Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis
- 1Strategic Research Centre for Molecular and Medical Research, School of Life and Environmental Sciences, Deakin University, Burwood, VIC, Australia
- 2Centre for Cellular and Molecular Biology, School of Life and Environmental Sciences, Deakin University, Burwood, VIC, Australia
- 3Oxidation Biology Unit, Florey Institute of Neuroscience and Mental Health, Parkville, VIC, Australia
- 4Centre for Neuroscience Research, The University of Melbourne, Parkville, VIC, Australia
Over the past two decades there have been significant advances in our understanding of copper homeostasis and the pathological consequences of copper dysregulation. Cumulative evidence is revealing a complex regulatory network of proteins and pathways that maintain copper homeostasis. The recognition of copper dysregulation as a key pathological feature in prominent neurodegenerative disorders such as Alzheimer’s, Parkinson’s, and prion diseases has led to increased research focus on the mechanisms controlling copper homeostasis in the brain. The copper-transporting P-type ATPases (copper-ATPases), ATP7A and ATP7B, are critical components of the copper regulatory network. Our understanding of the biochemistry and cell biology of these complex proteins has grown significantly since their discovery in 1993. They are large polytopic transmembrane proteins with six copper-binding motifs within the cytoplasmic N-terminal domain, eight transmembrane domains, and highly conserved catalytic domains. These proteins catalyze ATP-dependent copper transport across cell membranes for the metallation of many essential cuproenzymes, as well as for the removal of excess cellular copper to prevent copper toxicity. A key functional aspect of these copper transporters is their copper-responsive trafficking between the trans-Golgi network and the cell periphery. ATP7A- and ATP7B-deficiency, due to genetic mutation, underlie the inherited copper transport disorders, Menkes and Wilson diseases, respectively. Their importance in maintaining brain copper homeostasis is underscored by the severe neuropathological deficits in these disorders. Herein we will review and update our current knowledge of these copper transporters in the brain and the central nervous system, their distribution and regulation, their role in normal brain copper homeostasis, and how their absence or dysfunction contributes to disturbances in copper homeostasis and neurodegeneration.
Copper is indispensable for normal development and function of the central nervous system (CNS). The copper concentration of the human adult brain is significant, estimated at 7–10% of total body copper, similar to that of the liver, the major organ that regulates the copper status of the body (Cartwright and Wintrobe, 1964; Linder, 1991). Regional variance in brain copper concentrations reflects differing metabolic requirements for copper, which change during development (reviewed in Lutsenko et al., 2010). Copper is required as a cofactor for numerous critical enzymes that are involved in vital CNS processes such as respiration, neurotransmitter synthesis, activation of neuropeptides and hormones, protection from oxidative damage, myelination, pigmentation, and iron metabolism among others. The redox cycling of copper between Cu2+ and Cu+ oxidation states is utilized by enzymes involved in these processes for catalytic reactions. However, this redox activity also can lead to elevated reactive oxygen species (ROS) and corruption of critical proteins by adventitious binding of copper ions (Halliwell and Gutteridge, 1984). High oxygen consumption in the brain (20% of total body oxygen), coupled with low levels of antioxidants and antioxidant enzymes, and high levels of metal ions, mean the brain is particularly susceptible to ROS-induced oxidative stress. Hence, precise regulation of brain copper is essential to ensure appropriate levels and distribution for the maintenance of brain function, without risking inadvertent interactions with other cellular components.
Much of what is currently known about brain copper regulation comes from studies of diseases where copper dysregulation is associated with neurodegeneration. Menkes disease (MD; OMIM 309400) is an X-linked inherited disorder with serious neurological symptoms and neurodegeneration resulting from severe copper deficiency. Occipital horn syndrome (OHS; OMIM 304150) is an allelic variant of MD with milder neurological symptoms and predominantly connective tissue defects. In Wilson disease (WD; OMIM 277900), an inherited, autosomal recessive copper toxicosis disorder, patients present with hepatic and neurological symptoms (reviewed in Danks, 1995). There is mounting evidence that copper dysregulation plays a key role in more common neurodegenerative diseases such as Alzheimer’s, Parkinson’s, Huntington’s, motor neuron, and prion diseases (reviewed in Scheiber et al., 2013).
The mechanisms of brain copper import, distribution, and export are now beginning to be elucidated. The exchange of copper between the periphery and the brain is highly regulated by the brain barriers. The copper concentration of cerebrospinal fluid (CSF; ~0.25 μM; Kjellin, 1963; Lentner, 1981) is up to 100-fold lower than that in the plasma (11–25 μM; Tietz, 1987). In a rat brain perfusion study that compared copper uptake into brain capillaries, parenchyma, choroid plexus, and CSF, non-protein bound free copper ion was the predominant copper species that entered the brain via both the blood–brain barrier (BBB) and the blood–CSF barrier (BCB; Choi and Zheng, 2009). The higher rate of copper transport into the brain parenchyma compared to the CSF suggests that the BBB is the main site through which copper enters the brain. Copper influx into the brain parenchyma and CSF is regulated by copper transporters CTR1, ATP7A, and ATP7B, which are highly expressed in the brain capillaries and choroid plexus (Iwase et al., 1996; Qian et al., 1998; Kuo et al., 2006; Niciu et al., 2006; Choi and Zheng, 2009; Donsante et al., 2010; Davies et al., 2013).
Significant insight into the mechanisms controlling brain copper homeostasis began two decades ago with the identification of the genes encoding the essential copper-transporting ATPases, ATP7A (Chelly et al., 1993; Mercer et al., 1993; Vulpe et al., 1993) and ATP7B (Bull et al., 1993; Petrukhin et al., 1993; Yamaguchi et al., 1993). Mutations in ATP7A and ATP7B underlie MD and WD, respectively. ATP7A is located on chromosome Xq13.2-13.3 and comprises 23 exons that span approximately 150 kb1. ATP7B is located on chromosome 13q14.3 and comprises 21 exons that span approximately 80 kb2. Transcripts of approximately 7.5–8.5 kb are produced from both genes and contain coding regions of 4.5 kb, which are translated to produce proteins of 180 and 165 kDa, respectively. ATP7A and ATP7B are members of the P1B-subfamily of the P-type ATPases. They undergo ATP-dependent cycles of phosphorylation and dephosphorylation to catalyze the translocation of copper across cellular membranes. Their structure and biochemistry was thoroughly reviewed by Lutsenko et al. (2007). They are highly related in structure and function with approximately 60% amino acid identity. They have eight transmembrane domains that form a path through cell membranes for copper translocation; and a large N-terminus with six metal-binding domains (MBDs), each comprising approximately 70 amino acids and the highly conserved metal-binding motif GMxCxxC (where x is any amino acid). Other highly conserved domains include the intramembrane CPC motif that is required for copper translocation through the membrane, the N-domain containing the ATP-binding site, the P-domain containing the conserved aspartic acid residue and the A-domain comprising the phosphatase domain. Copper-binding together with other N- and C-terminal signals regulate their activity, intracellular location, and copper-induced intracellular trafficking (see below and reviewed in La Fontaine and Mercer, 2007; Lutsenko et al., 2007; Figure 1).
FIGURE 1. Schematic diagram of the copper-ATPases, ATP7A and ATP7B. Shown are the highly conserved domains: the N-terminal copper-binding domain, the phosphatase (A-domain), phosphorylation (P-domain), and ATP-binding (N-domain) domains; and the motifs and sequences required for their localization and trafficking. The cylindrical regions labeled 1 -8 represent the transmembrane domains.
ATP7A and ATP7B possess dual functions, delivering copper for incorporation into copper-dependent enzymes, and removal of excess copper from cells. These functions are largely regulated by their sub-cellular localization (see below). ATP7A is ubiquitously expressed in extrahepatic cells and tissues, which explains the systemic defects caused by its absence or inactivation in MD and points to a house-keeping role for ATP7A. ATP7B has a more limited expression pattern, with the highest expression level in the liver, and lower levels in the kidney, placenta, brain, heart, and lungs (Bull et al., 1993; Tanzi et al., 1993; Vulpe et al., 1993). This restricted expression suggests more specialized functions for ATP7B in regulating copper physiology, such as biliary copper excretion (Terada et al., 1999). ATP7B also has a biosynthetic role, supplying copper to cuproenzymes such as ceruloplasmin (Terada et al., 1998). In cells where ATP7B is co-expressed with ATP7A, it often has a specific and distinct role (Veldhuis et al., 2009a; La Fontaine et al., 2010), for example in copper secretion into milk during lactation (Michalczyk et al., 2008), and in fine-tuning the intracellular copper balance in the kidney (Linz et al., 2008; Barnes et al., 2009). The expression of both copper-transporting P-type ATPases (copper-ATPases) in the brain and the severe neurological symptoms that arise from a deficiency of either transporter, suggest that they play key roles in regulating brain copper homeostasis. This review will summarize our current knowledge of the expression, localization, and contribution of ATP7A and ATP7B to maintaining and managing copper levels within the brain.
Expression and Localization of ATP7A and ATP7B in the Brain
The ATP7A gene is transcribed to produce an 8.5 kb transcript that is expressed in all tissues examined except for the liver (Chelly et al., 1993; Vulpe et al., 1993). In the mouse brain, the Atp7a transcript is expressed in the cerebrovascular endothelial (CVE) cells that form the BBB (Qian et al., 1998), and is strongly expressed in the choroid plexus (Kuo et al., 1997; Murata et al., 1997; Nishihara et al., 1998; Choi and Zheng, 2009), a structure that forms the BCB and regulates the concentration of substances in the CSF (Figure 2A). Choi and Zheng (2009) further showed that Atp7a is more highly expressed in the brain barriers (BBB and BCB), the brain capillaries and choroid plexus, than in brain parenchyma. Comparing the two barriers, Atp7a mRNA expression is 3.4-fold higher in the choroid plexus than in the cerebral capillaries. This observation is consistent with the finding that the Atp7a protein levels in the developing and adult mouse brain are highest in the choroid plexus/ependymal cells of the lateral and third ventricles (Niciu et al., 2006).
FIGURE 2. Schematic diagram illustrating the proposed mechanisms of copper transport across the blood brain barrier (BBB) and blood cerebrospinal fluid barrier (BCB). (A) Copper transport under physiological conditions. Copper import into cells is via the major copper import protein CTR1. The proposed locations and orientation of ATP7A and ATP7B are shown. ATP7A is expressed in cerebrovascular endothelial cells that form the BBB but its expression is 3.4-fold higher in the choroid plexus than in the cerebral capillaries. In both choroid plexus epithelial cells and capillary endothelial cells of the brain, ATP7A predominantly localizes to the basolateral membrane. ATP7A facilitates copper transport from the blood across the BBB to the brain parenchyma. At the choroid plexus, ATP7A facilitates the removal of excess copper from the brain into the blood. Therefore, the BCB serves as the main pathway for eliminating excess brain copper. In contrast, ATP7B is concentrated at the apical membrane. At the CSF-facing apical membrane of choroid plexus epithelial cells, ATP7B may contribute to copper transport into the CSF and copper sequestration in the choroid plexus. Astrocytes are the first brain parenchyma cells to encounter metal ions that cross the BBB and play an important role in copper transport from the blood and CSF toward neurons. Copper transport in glutamatergic neurons is depicted. Copper-independent and reversible trafficking of ATP7A is stimulated by N-methyl-D-aspartate receptor (NMDAR) activation that leads to Ca2+ influx and is associated with the rapid release of copper from neurons. The released copper down-regulates NMDAR activity thus protecting neurons from excitotoxicity. (B) Perturbed copper transport in Menkes disease due to the absence or inactivation of ATP7A. The predicted consequences of ATP7A inactivation in relation to copper levels in brain barrier cells, astrocytes and neurons are shown. Any copper that reaches the BBB accumulates within endothelial cells leading to reduced copper transport to the brain parenchyma, astrocytes and neurons. Any copper that reaches astrocytes also will accumulate. There is reduced copper transport across the BCB. Excitotoxicity due to impaired synaptic copper release from glutamatergic neurons, which down-regulates NMDAR activity, can contribute to seizures and neuronal degeneration in Menkes disease.
Based on abnormal copper accumulation in cultured astrocytes from the macular mouse, a model of MD, Kodama et al. (1991) proposed that astrocytes play an important role in copper transport from the blood and CSF toward neurons, and that this pathway is disturbed in MD and animal models (Figure 2B). Kaler and Schwartz (1998) later confirmed the expression of mouse and rat Atp7a in astrocytes from various brain regions (cerebral cortex, corpus striatum, and cerebellum). Therefore, ATP7A is postulated to play a key role in the copper distribution from astrocytes to neurons. Importantly, the successful treatment of MD mouse models by intravenous administration of copper earlier than postnatal day 7 (P7; Mann et al., 1979) was proposed to be a consequence of the immaturity of the BBB, which includes astrocytes (Kodama et al., 1991). This immaturity allows the penetration of copper that is prevented in these ATP7A-deficient models once development of the BBB is complete.
Early in situ hybridization studies in mouse brain showed significant levels of the Atp7a transcript in the hippocampal CA1 region, the dentate gyrus, the cerebellar granular layer and the olfactory bulb, and lower levels in the hippocampal CA3 region and Purkinje neurons (Iwase et al., 1996). Atp7a mRNA was detected also by RT-PCR in mouse and rat cerebral cortex and cerebellum, and in isolated rat cerebellar granule neurons (Kaler and Schwartz, 1998). Consistent with these observations, a detailed immunohistochemical study by Niciu et al. (2006) demonstrated the presence of the Atp7a protein in most CNS cell types at P11 in the developing mouse brain and in the adult brain. In transgenic mice that overexpressed human ATP7A, the protein is primarily produced in the CA2 region of the hippocampus, the Purkinje neurons of the cerebellum, and in the choroid plexus (Ke et al., 2006). The overexpression of ATP7A resulted in an overall reduction of brain copper concentrations (Ke et al., 2006), which is consistent with ATP7A in the choroid plexus functioning to efflux copper back into the circulation (Choi and Zheng, 2009). In more recent studies of human brain tissue, ATP7A protein levels are most prominent in the cerebellum and substantia nigra (Davies et al., 2013). The significance of ATP7A expression in these brain regions is poorly understood.
ATP7A expression is developmentally regulated (Kuo et al., 1997; Barnes et al., 2005; El Meskini et al., 2005; Niciu et al., 2006). The widespread expression of Atp7a mRNA in neurons and ependymal cells during embryonic and postnatal development in the mouse (Kuo et al., 1997; Murata et al., 1997) suggests a house-keeping role for ATP7A in the brain and CNS. Interestingly, Atp7a is not detectable by RT-PCR in embryonic day 20 rat astrocytes, but it is detectable in P3, P8, and adult astrocytes (Kaler and Schwartz, 1998). The study by Niciu et al. (2006) showed that Atp7a protein levels are most abundant in the early postnatal period, peaking in the neocortex and cerebellum at P4. From birth (P0) to adulthood, there is a decline in Atp7a levels in most brain regions, and this decline is more pronounced in the hippocampus and cerebellum than in the hypothalamus (Niciu et al., 2006). During this postnatal period, despite a general decline in Atp7a levels, there is increased Atp7a expression in CA2 hippocampal pyramidal cells and cerebellar Purkinje neurons. The authors proposed that since the CA2 region is resistant to epileptogenesis, the increase in CA2 Atp7a levels may contribute to seizure resistance (Niciu et al., 2006). The observed increase in Atp7a levels in Purkinje neurons is consistent with significant levels of ATP7A in human cerebellar Purkinje neurons (Davies et al., 2013), but it is inconsistent with other reports of a postnatal decline in mouse Atp7a mRNA and protein levels in these cells (Iwase et al., 1996; Barnes et al., 2005). Although Barnes et al. (2005) reported a postnatal switch in the expression of Atp7a from Purkinje neurons to Bergmann glia in the rodent brain, in human brain tissue, ATP7A could not be detected in the Bergmann glia (Davies et al., 2013). This discrepancy may allude to the possibility that different mechanisms regulate human and rodent cerebellar copper homeostasis. The increased ATP7A expression in the cerebellum may explain the increased sensitivity of this region, and in particular Purkinje neurons, to copper deficiency as observed in MD (Menkes et al., 1962; Kumode et al., 1993, 1994; Iwase et al., 1996; Geller et al., 1997; Liu et al., 2005a; Niciu et al., 2006).
In the olfactory system, neuronal Atp7a localization correlates with neuronal maturation. Atp7a is initially concentrated in neuronal cell bodies at early embryonic stages, then shifts to the extending axons during the postnatal period (El Meskini et al., 2005). Atp7a levels peak prior to synaptogenesis, which occurs postnatally. Similarly, increased expression levels precede synapse formation following injury-stimulated neurogenesis. Together with a follow-up study of the mottled brindled mouse model of MD (MoBr/y), these data suggest a role for ATP7A in axon extension and synaptogenesis, the absence of which may contribute to the neurodegeneration evident in MD and its mouse models (El Meskini et al., 2007).
The increase in ATP7A during the early postnatal period indicates a crucial role for copper during early development, and particularly in synaptogenesis. This may underlie the critical window during which some human MD patients and mouse models (the mottled mouse mutants) respond favorably to postnatal copper injections, especially when administered in the early postnatal period (Mann et al., 1979; Fujii et al., 1990; Niciu et al., 2006, 2007; Tang et al., 2008). Kaler et al. (2008) reported that this successful copper treatment depends on the presence of a mutant ATP7A protein with some residual copper transport function. Hence, the therapeutic efficacy of copper injections may be a consequence of increased levels of mutant ATP7A, albeit with significantly reduced catalytic activity (La Fontaine et al., 1999; Kaler, 2011).
A zebrafish mutant, calamity, with an embryonic-recessive lethal mutation in the ATP7A ortholog, shows impaired copper homeostasis with absent melanin pigmentation, defective notochord formation, and neurodegeneration in the hindbrain region of the developing brain (Mendelsohn et al., 2006; Madsen et al., 2008). These authors proposed a developmental hierarchy of copper metabolism, where notochord formation is preferentially preserved during copper limitation, potentially explaining some of the vascular and neurologic abnormalities observed in MD. Drosophila has a sole ortholog of ATP7A, DmATP7, which appears to play an important role in the developing Drosophila brain (Norgate et al., 2007). It is strongly expressed in the larval brain at different developmental stages (Burke et al., 2008). Strong DmATP7A expression is observed in the ventral ganglion but it is absent from most of the optic lobes (Burke et al., 2008).
Although ATP7B is expressed in the brain (Bull et al., 1993; Tanzi et al., 1993), its expression patterns and contribution to brain copper homeostasis are less well characterized than that of ATP7A. In the brain of the developing mouse embryo, Atp7b mRNA cannot be detected, suggesting that there may be no prenatal expression or that expression is below the detection limits (Kuo et al., 1997). Alternatively, consistent with the possibility that significant expression begins postnatally, brain copper levels in an Atp7b null mouse continues to increase slightly throughout adult life (Buiakova et al., 1999). In a study of Atp7b protein and mRNA distribution in the rat brain, Atp7b is detected in the hippocampus, the granular cells of the dentate gyrus and pyramidal cells of the CA1 to CA4 layers, the glomerular cell layer of the olfactory bulbs, Purkinje neurons of the cerebellum, pyramidal neurons of the cerebral cortex, and cores of several nuclei (e.g., pontine nuclei and lateral reticular nuclei) in the brainstem (Saito et al., 1999). In these brain regions, both Atp7b mRNA and protein correlate with copper distribution as determined by staining with the copper chelator bathocuproine disulfonic acid (BCS). Based on similar distribution patterns of cuproenzymes such as dopamine-β-hydroxylase (DBH) and Cu–Zn superoxide dismutase (Cu–Zn SOD), as well as abnormal catecholamine synthesis in the Long-Evans Cinnamon (LEC) rat model of WD (Saito et al., 1996; Okabe et al., 1998), these authors speculated that ATP7B-mediated control of copper homeostasis in these brain regions is important in regulating DBH activity.
In contrast to mouse Atp7a, there is continuous Atp7b expression in the adult mouse cerebellar Purkinje neurons, and an age-dependent down-regulation (Barnes et al., 2005). Based on kinetic studies and experiments in mice lacking Atp7b, these authors proposed a homeostatic role for ATP7A in maintaining intracellular copper at a certain level, and a biosynthetic role for ATP7B mediating the synthesis of copper-dependent enzymes such as ceruloplasmin (Barnes et al., 2005).
In the human brain, immunohistochemical staining reveals expression of the ATP7B protein in the visual cortex, anterior cingulate cortex, body of caudate, putamen, substantia nigra, and cerebellum, with the most significant levels of ATP7B detected in the cerebellum, anterior cingulated cortex, and caudate putamen (Davies et al., 2013). Strong staining of ATP7B in Purkinje neurons and not the Bergmann glia is consistent with the findings in the adult rat and mouse brains. However, there is no correlation between ATP7A and ATP7B protein levels and copper levels in the brain regions investigated (Davies et al., 2013).
Function and Regulation of the Copper-ATPases in CNS Cell Types
Regulation of ATP7A and ATP7B
Much of what is currently known about the copper-ATPases derives from studies in peripheral cells and tissues. Emerging studies of copper transport and the copper-ATPases in the brain and certain CNS cell types both support our current understanding of their mechanism of action and regulation, but also provide new insights into the complexity of copper’s role in the CNS.
ATP7A and ATP7B have a dual role in cells; a biosynthetic role, delivering copper to the secretory pathway for metallation of cuproenzymes, and a homeostatic role, exporting excess copper from the cell. Under normal, physiological conditions, ATP7A and ATP7B are localized at the trans-Golgi network (TGN) where they provide copper to copper-dependent enzymes synthesized in the secretory pathway. ATP7A has a role in the metallation of enzymes such as peptidylglycine α-amidating monooxygenase (PAM; El Meskini et al., 2003; Steveson et al., 2003), tyrosinase (Petris et al., 2000; Setty et al., 2008), extracellular SOD3 (Qin et al., 2005), DBH (Saito et al., 1996), and lysyl oxidase, all of which are expressed in the CNS (Lutsenko et al., 2010). ATP7A-mediated copper delivery to lysyl oxidase is proposed based on similar temporal expression of these two proteins in the developing rat brain and the sensitivity of lysyl oxidase-dependent processes to ATP7A inactivation as evident in MD and OHS (Royce et al., 1980; Kuivaniemi et al., 1985; Kaler et al., 1994; Kaler, 1998; Tchaparian et al., 2000; Lutsenko et al., 2007). Copper delivery to apo-ceruloplasmin in hepatocytes (Terada et al., 1998) and mouse cerebellum (Barnes et al., 2005) is mediated by Atp7b, and by Atp7a in macrophages in response to hypoxia-mediated increased copper uptake (White et al., 2009).
The key mechanism by which the copper-ATPases regulate cellular copper levels involves alteration of their cellular localization in response to changes in cytoplasmic copper concentration. When intracellular copper levels are elevated, ATP7A and ATP7B traffic from the TGN to the cell periphery to export excess copper from cells. The copper-induced trafficking of ATP7A was first described in Chinese hamster ovary (CHO-K1) cells (Petris et al., 1996), and since then, it has been reported in a wide range of non-polarized (e.g., human fibroblasts, HeLa, and mammary carcinoma cells; Yamaguchi et al., 1996; Ackland et al., 1997; Dierick et al., 1997; Francis et al., 1998; La Fontaine et al., 1998a,b; Qi and Byers, 1998) and polarized cell types (Madin–Darby canine kidney (MDCK), mouse enterocytes, Caco-2; Greenough et al., 2004; Monty et al., 2005; Nyasae et al., 2007). Trafficking of ATP7B also has been observed in non-polarized hepatoma, human bladder carcinoma, and CHO-K1 cells (Hung et al., 1997; Yang et al., 1997; Forbes and Cox, 2000; La Fontaine et al., 2001; Huster et al., 2003), and in polarized hepatic cells (HepG2 and WIF-B; Roelofsen et al., 2000; Guo et al., 2005; Cater et al., 2006).
In polarized cells, ATP7A traffics from the TGN to a rapidly recycling vesicular pool located near the basolateral membrane (Monty et al., 2005; Nyasae et al., 2007), whereas ATP7B traffics to sub-apical vesicles (Roelofsen et al., 2000; Guo et al., 2005; Cater et al., 2006). At these locations they sequester and mediate the export of excess copper. When copper levels return to normal, ATP7A and ATP7B recycle back to the TGN (Petris and Mercer, 1999; Cater et al., 2006; Nyasae et al., 2007). The trafficking and recycling of the copper-ATPases requires specific signal sequences (Figure 1). For both ATP7A and ATP7B, only MBD 5 or 6 is necessary and sufficient to mediate copper-stimulated trafficking from the TGN to the cell periphery (Strausak et al., 1999; Cater et al., 2004). C-terminal di- and tri-leucine motifs in ATP7A and ATP7B, respectively, are required for retrograde trafficking of the proteins to the TGN when copper levels return to normal (Petris et al., 1998; Cater et al., 2006; Braiterman et al., 2011), and for basolateral targeting of ATP7A in polarized MDCK cells (Greenough et al., 2004). TGN retention of ATP7A is mediated by a 38 amino acid sequence contained within transmembrane domain three (Francis et al., 1998) whereas ATP7A retention at the basolateral surface may require the PDZ-binding motif (D1497TAL) within the C-terminus (Greenough et al., 2004). In ATP7B, a nine amino acid sequence (F37AFDNVGYE) in the N-terminus is essential for TGN retention under low copper conditions and for apical targeting in polarized hepatocytes when copper levels are elevated (Braiterman et al., 2009). Although details of the trafficking machinery involved in these processes remain to be fully elucidated, interacting partners that may play a role include AIPP1, a PDZ domain-containing protein that may bind to the PDZ motif in ATP7A (Stephenson et al., 2005), and dynactin subunit p62 that may be involved in ATP7B trafficking (Lim et al., 2006b).
In addition to the N- and C-terminal signals that control the copper-ATPase response to elevated copper, other processes also contribute to regulating copper-ATPase activity. They include, posttranslational modifications such as transient auto-phosphorylation at the invariant aspartate residue (D1044KTGT; Figure 1) to form an acyl-phosphate intermediate, a process that is characteristic of the P-type ATPase catalytic cycle (Voskoboinik et al., 1998, 2001a,b; Petris et al., 2002; Tsivkovskii et al., 2002; Cater et al., 2007), copper-stimulated phosphorylation by kinases (Vanderwerf et al., 2001; Voskoboinik et al., 2003; Veldhuis et al., 2009b), and protein interactions. ATOX1 was the first protein shown to interact in a copper-dependent manner with the N-terminal domain of both proteins for delivery of copper to the secretory pathway (Hamza et al., 1999; Larin et al., 1999). MBD 1–4 is most important for this interaction, in particular MBD 2 and 4 (Strausak et al., 2003; Walker et al., 2004; Achila et al., 2006). This is supported by studies in the Atox1 null mice, which demonstrated a critical requirement for Atox1 in Atp7a function and copper homeostasis (Hamza et al., 2001, 2003). A 45 kDa isoform of the promyelocytic leukemia zinc finger (PLZF) protein, a transcriptional repressor of Hox genes, interacts with the C-terminus of ATP7B (Ko et al., 2006). Both proteins co-localized within the TGN, and based on experiments in HepG2 cells and Drosophila, this interaction is proposed to have a role in regulating ERK signal transduction. However, the functional consequences of these associations remain to be elucidated. The glutaredoxin1 (GRX1)/glutathione (GSH) system may play a key role in regulating the trafficking and activity of the copper-ATPases by regulating their redox state through glutathionylation and deglutathionylation by GRX1 (Lim et al., 2006a; Singleton et al., 2010). GRX1 protects proteins from oxidative damage (Mieyal et al., 2008), and it is expressed throughout the brain with highest activity in the hippocampus, cortex and midbrain (Balijepalli et al., 1999; Ehrhart et al., 2002; Aon-Bertolino et al., 2011). Hence, GRX1/GSH may preserve the integrity and function of ATP7A and ATP7B during oxidative stress, which accompanies neuropathological processes. Clusterin (ApoJ) and COMMD1 regulate the degradation of misfolded and mutant copper-ATPases via the lysosomal and proteasomal pathways, respectively (de Bie et al., 2007; Materia et al., 2011, 2012).
Role of the Copper-ATPases in CNS Cell Types
Information on the activity of the copper-ATPases in specific CNS cell types is limited and somewhat fragmentary, but emerging evidence is revealing specific roles for ATP7A and ATP7B in brain and CNS copper homeostasis. Peripherally, ATP7A and ATP7B mostly have cell type-specific expression patterns and where co-expressed in certain cells and tissues (e.g., kidney, placenta, and mammary gland), they have distinct roles (reviewed in La Fontaine and Mercer, 2007 and Veldhuis et al., 2009a). Similarly in the CNS, ATP7A and ATP7B may be uniquely expressed in certain cell types and co-expressed in others.
Choroidal Epithelial Cells and Brain Capillary Endothelial Cells
The BBB and BCB regulate the movement of copper between the brain and peripheral circulation. In both choroid plexus epithelial cells and capillary endothelial cells of the brain, ATP7A predominantly localizes to the basolateral membrane, which is consistent with its location in other polarized epithelial cell types such as intestinal enterocytes (Monty et al., 2005; Nyasae et al., 2007; Davies et al., 2013). In contrast, ATP7B is concentrated at the apical membrane, again consistent with its localization in polarized hepatocytes (Roelofsen et al., 2000; Guo et al., 2005; Cater et al., 2006; Davies et al., 2013). This distinct membrane localization of ATP7A and ATP7B combined with their discrete enzyme kinetics may be a mechanism to ensure strict control over copper transport across the BCB and BBB (Tsivkovskii et al., 2002; Barnes et al., 2005; Hung et al., 2007). The kinetically slower ATP7B at the CSF-facing apical membrane of choroid plexus epithelial cells may explain the slower rate of copper transport into the CSF relative to the choroid plexus copper uptake rate, and may contribute to copper sequestration in the choroid plexus (Barnes et al., 2005, 2009; Choi and Zheng, 2009). In contrast, the basolateral location of the kinetically faster ATP7A facilitates the removal of excess copper from the brain into the blood (Davies et al., 2013). This arrangement of the copper-ATPases is similar to that in other tissues such as the mammary epithelium or the kidney where ATP7A serves to protect from copper excess while ATP7B serves a biosynthetic role (La Fontaine and Mercer, 2007; Veldhuis et al., 2009a). Therefore, the BCB serves as the main pathway for eliminating excess brain copper (Figure 2). In a further study that utilized cultured choroidal epithelial Z310 cells, siRNA-mediated knockdown of ATOX1 and ATP7A resulted in increased cellular copper retention, confirming the involvement of ATP7A in copper transport across the choroid plexus and hence in regulating copper homeostasis of the CSF (Monnot et al., 2012). The BBB, which regulates copper influx into the brain, has lower levels of ATP7A at the basolateral surface of brain capillary endothelial cells to enable rapid but limited transport of copper into the brain to accommodate sudden changes in brain copper concentration (Choi and Zheng, 2009).
Astrocytes play a pivotal role in brain copper homeostasis. They are strategically sandwiched between endothelial cells of the BBB and neurons, hence, they are the first brain parenchyma cells to encounter metal ions that cross the BBB. Astrocytes are able to efficiently take up and store copper, and with greater resistance to copper-induced toxicity, they protect neurons from copper toxicity (reviewed in Tiffany-Castiglioni et al., 2011; Scheiber and Dringen, 2012). Atp7a has been detected in rodent astrocytes in culture and in brain tissue (Qian et al., 1997; Barnes et al., 2005; Niciu et al., 2007; Scheiber et al., 2012). These studies implicate Atp7a in copper export from astrocytes, which is consistent with the early observations by Kodama et al. (1991) of copper accumulation in astrocytes of the macular mouse (Figure 2B). In astrocytes, similar to peripheral cell types, Atp7a localizes to a perinuclear region and undergoes copper-responsive trafficking between the TGN and the cell periphery. Therefore, it was proposed that Atp7a mediates copper export from astrocytes, which is time-, concentration- and temperature-dependent (Scheiber et al., 2012). However, in contrast to previous studies, copper export from cultured astrocytes is non-saturable and does not follow the established Michaelis–Menten kinetics for ATP7A-dependent copper transport (Scheiber et al., 2012). Therefore, additional ATP7A-independent mechanisms may be involved in copper export from astrocytes. The rate of copper export is proportional to the increase in copper content after copper exposure, which led Scheiber et al. (2012) to propose that the copper export rate is determined by the trafficking or fusion of Atp7a-containing vesicles with the plasma membrane, rather than by ATP7A-mediated transport of copper into vesicles.
Cerebellar Purkinje neurons are highly sensitive to copper deficiency during development (Lyons and Prohaska, 2009). In the human brain, ATP7A and ATP7B are co-expressed in Purkinje neurons (Davies et al., 2013), and in the mouse brain, for a postnatal period of up to 2 weeks (Barnes et al., 2005). Co-expression of both copper-ATPases may be a mechanism to achieve a delicate balance of copper that is critical to cerebellar development and function. Based on the faster kinetics of copper transport by Atp7a relative to Atp7b, a homeostatic role is proposed for Atp7a in maintaining the intracellular copper level, and a biosynthetic role for Atp7b to mediate the synthesis of copper-dependent enzymes such as ceruloplasmin (Barnes et al., 2005).
Hippocampal ATP7A plays a pivotal role in learning and memory. In mature rat primary hippocampal neurons, Atp7a undergoes both copper-dependent and -independent redistribution from the TGN to dendrites and axons (Schlief et al., 2005). The study by Schlief et al. (2005) provides the first evidence of copper-independent and reversible trafficking of Atp7a that (i) is stimulated by N-methyl-D-aspartate (NMDA) receptor activation, (ii) requires Ca2+ influx through the NMDA receptor, and (iii) is associated with the rapid release of copper from hippocampal neurons (Figure 2A). The inability to detect Atp7a at the cell surface prompted the suggestion that copper may be released by exocytosis from vesicles once Atp7a has recycled back to the TGN. This possibility is consistent with the rapid efflux of copper following NMDA receptor activation. The authors suggest that NMDA receptor activation-mediated trafficking of copper-loaded, ATP7A-associated vesicles provides a readily available and releasable pool of copper following Ca2+ influx (Schlief et al., 2005). In the hippocampus, following neuronal depolarization, about 15 μM of copper is released into the glutamatergic synaptic cleft from synaptic vesicles (Rajan et al., 1976; Hartter and Barnea, 1988; Kardos et al., 1989; Barnea et al., 1990; Hopt et al., 2003). While the physiological significance of synaptic copper release is not yet clear, it is proposed that copper down-regulates NMDA activity through redox processes that involve S-nitrosylation of specific cysteine residues within NMDA subunits NR1 and NR2A, thus protecting hippocampal neurons from excitotoxicity (Schlief et al., 2006). These findings link ATP7A and copper with modulating memory and learning processes that depend on precise regulation of NMDA receptor activity (Schlief et al., 2006). In MD, deficiencies in both brain copper and ATP7A activity will prevent copper release, thus impairing NMDA receptor modulation. The subsequent NMDA-mediated excitotoxicity may contribute to the pathological features, seizures and neuronal degeneration, that are characteristic of MD (Schlief et al., 2006). In Alzheimer’s disease (AD), the combination of increased copper and Aβ [the amyloidogenic cleavage product of the amyloid precursor protein (APP)] in the synaptic cleft may promote the formation of neurotoxic Aβ-copper oligomers contributing to the neuropathology of AD.
The recent identification of a new ATP7A-related distal hereditary motor neuropathy (dHMN), caused by mutations in ATP7A (see below), has drawn attention to the role of ATP7A in motor neurons (Kennerson et al., 2010; Yi et al., 2012). The cell bodies of motor neurons are located within the anterior horn of the spinal cord, and their axons extend for long distances to distal limb muscles. Hence, both the CNS and peripheral nervous system are affected in motor neuron disorders (Harding and Thomas, 1980). In undifferentiated NCS-34 cells (a motor neuron-enriched cell line), Atp7a is localized at the TGN and traffics to the cell periphery with elevated copper, as it does in most other cell types. In differentiated NSC-34 cells, Atp7a can be detected along the full length of Tau-1-positive neuritic projections, with localization to the axonal membrane when copper levels are elevated (Yi et al., 2012). Based on the data presented, ATP7A was postulated to traffic along axons, and to mediate copper release from the axonal membrane of motor neurons.
Retinal Pigment Epithelium
Retinal degeneration is observed in both MD and WD (Ferreira et al., 1998). The essential requirement for copper and ATP7B for retinal structure integrity is underscored by reduced thickness of total macula as well as ganglion cell and inner plexiform layer in WD patients. Up to 50% of WD patients have abnormal visual evoked potentials (VEPs; Albrecht et al., 2012). Immunohistochemical studies of mouse and human retina identified the presence of ATP7A in the retinal pigment epithelium (RPE), outer plexiform layer (OPL), and ganglion cell layer (GCL) of the BALB/c mouse retina (Krajacic et al., 2006). In contrast, ATP7B expression is restricted to the RPE. Within the RPE, both copper-ATPases localize to a perinuclear region that overlap with TGN and Golgi markers, consistent with their biosynthetic role in delivering copper to tyrosinase for melanogenesis, and to the iron homeostatic proteins ceruloplasmin and hephaestin. Increased copper levels trigger a redistribution of ATP7B to a diffuse cytoplasmic compartment in an immortalized human RPE cell line.
Activated microglial cells concentrate at sites of neuronal damage and inflammation. Atp7a expression is elevated in activated microglia surrounding Aβ plaques in the TgCRND8 transgenic mouse model of AD (Zheng et al., 2010). Data from cultured mouse BV-2 microglial cells suggest Atp7a expression and trafficking is responsive to stimulation by the pro-inflammatory cytokine interferon-gamma (IFN-γ). Concomitant copper accumulation due to upregulation of the copper import protein, Ctr1 and copper uptake, suggests a role for copper in the pro-inflammatory pathway. Furthermore, the IFN-γ-stimulated ATP7A redistribution differs from that induced by copper, and appears to mediate copper sequestration in cytoplasmic vesicles rather than copper export. This mechanism is postulated to represent a protective mechanism by activated microglia at sites of amyloidogenesis to reduce aberrant copper-Aβ interactions in the extracellular milieu (Zheng et al., 2010).
Pineal night-specific ATPase (PINA) is a novel splice variant of ATP7B, lacking the N-terminal MBDs and the first four transmembrane domains. It has a predominant nocturnal expression in the pineal gland and retina, under the control of the retina-specific protein, cone rod homeobox (CRX; Li et al., 1998). Despite a large N-terminal truncation, PINA retains a weak copper transport function in a Saccharomyces cerevisiae ccc2Δ complementation assay (Borjigin et al., 1999). This finding implicates a yet-to-be-defined role for PINA-mediated copper metabolism in pineal and retinal circadian function (Li et al., 1998; Borjigin et al., 1999).
Neuroblastoma cells have a high demand for copper for proliferation. High concentrations of copper in neuroblastoma cells are likely achieved via down-regulation of ATP7A expression and thus, reduced copper efflux. Retinoid treatment of neuroblastoma cells causes transcriptional upregulation of ATP7A and an increase in ATP7A protein levels (Liu et al., 2005b; Bohlken et al., 2009). Ectopic expression of the retinoic acid receptor β2 subtype (RARβ2) also induces ATP7A expression, which is associated a growth inhibitory effect. Conversely, knockdown of ATP7A is associated with reduced copper efflux and increased viability of retinoid-treated cells. These data support a model where malignant neuroblastoma cells have a high copper-dependency for viability and proliferation, and copper depletion by retinoid/RARβ2-induced ATP7A upregulation offers therapeutic benefit (Bohlken et al., 2009).
Functional Contribution of ATP7A and ATP7B to Brain Copper Homeostasis
An appreciation of the role of ATP7A and ATP7B in brain copper management derives largely from the functional consequences of their absence or inactivation in the genetically inherited diseases, MD, OHS, WD, and the recently identified ATP7A-related motor neuropathy. The importance of their correct function is also emerging in the context of other neurological diseases where there is perturbed copper metabolism, such as the prion diseases and AD. Our current understanding of the copper-ATPase contribution to brain copper homeostasis and the consequences of their absence or impaired function is summarized below.
Menkes Disease and Occipital Horn Syndrome
The widespread expression of ATP7A accounts for the systemic defects that arise from mutation of this gene in MD. This X-linked disease presents in males within the first few months of life, and in severe cases, it is fatal within 2–3 years. The severity of the clinical presentation can vary, but commonly includes abnormal neurodevelopment, seizures associated with cerebral atrophy and dysmyelination, a range of connective tissue and vascular abnormalities, fragile bones, an unusual kinky hair structure (pili torti), hair and skin pigmentation defects and failure to thrive (reviewed in Danks, 1995; Kaler, 2011). These symptoms arise from impaired intestinal copper absorption leading to systemic copper deficiency and consequently, reduced activity of critical copper-dependent enzymes. Paradoxically, copper retention is evident in certain tissues exposed to the limited copper that reaches them and in MD patient skin fibroblast cells (Camakaris et al., 1980; Danks, 1995). Histochemical analysis of brain tissue from affected MD patients revealed neurodegeneration in the cerebral cortex, cerebellum, and hippocampus (Okeda et al., 1991) where ATP7A is enriched (see above).
Occipital horn syndrome is also caused by mutations in ATP7A, but it is a milder disease with primarily connective tissue defects and moderate neurological symptoms (Kaler et al., 1994; Kaler, 1998). Causative mutations are often splice site mutations that result in reduced levels of normal ATP7A mRNA (reviewed in Kaler, 2011). The milder phenotype suggests that sufficient residual functional ATP7A is produced, but the prominent connective tissue defects indicate that copper delivery to lysyl oxidase is severely disrupted (Kaler, 2011; Scheiber et al., 2013).
The neurological symptoms of MD and OHS have been attributed to impaired ATP7A-mediated copper transport across the BBB (Figure 2B), leading to deficiencies of enzymes such as cytochrome c oxidase, SOD1, BDH, PAM, lysyl oxidase, and tyrosinase, some of which require ATP7A for metallation in the TGN. The bioactivity of many neuropeptides is dependent on their amidation by PAM, while DBH is important for the production of the neurotransmitter norepinephrine from dopamine (reviewed in Lutsenko et al., 2010; Kaler, 2011). However, impairment of other ATP7A-mediated functions also is likely to contribute to the neurodegeneration in MD. For example, excitotoxicity due to impaired synaptic copper release, which down-regulates NMDA receptor activity, can contribute to seizures and neuronal degeneration (Schlief et al., 2005, 2006; Figure 2). In MoBr/y mice, the absence of a functional ATP7A protein results in degeneration of Purkinje neurons, cytoskeletal abnormalities, and impaired synaptogenesis and axonal outgrowth (Niciu et al., 2006; El Meskini et al., 2007; Niciu et al., 2007).
There are a number of MD mouse models. As noted in the preceding sections, these mouse models have been invaluable in revealing insights into the critical role of ATP7A in the brain. The mottled mice are a series of mouse mutants with mutations in the murine ortholog of ATP7A. They exhibit a range of phenotypes that recapitulate the variable clinical severity of the human disease (Levinson et al., 1994; Mercer et al., 1994; Mercer, 1998). The MoBr/y mouse model resembles most closely classical MD with neurological deficits and early postnatal lethality. This mouse expresses close to normal levels of Atp7a that has severely reduced copper transport activity due to an in-frame deletion of six nucleotides, leading to the loss of highly conserved amino acids A799 and L800 (Grimes et al., 1997). Studies in this mouse elegantly demonstrated the importance of Atp7a in supplying copper to PAM for the amidation of neuropeptides (Steveson et al., 2003), in axon extension and synaptogenesis, and in compensatory mechanisms to facilitate copper transport across the BBB. The latter includes upregulation of the mutant Atp7a in endothelial cells, as well as increased association of MoBr/y astrocytes and microglia with the BBB, and these mechanisms possibly contribute to the effectiveness of early copper treatment (El Meskini et al., 2005, 2007; Niciu et al., 2007). The severe copper deficiency in the brain of MoBr/y mice can be rescued by transgenic expression of the human ATP7A. Expression of the ATP7A transgene was detected in the cerebellar Purkinje cell layer, the CA1 and CA2 regions of the hippocampus, the mitral layer of the olfactory bulb, the vascular endothelium, and the choroid plexus, but it could not be detected in astrocytes (Llanos et al., 2006). The gene correction significantly improved the survival of the ATP7A-expressing transgenic MoBr/y mice compared with non-transgenic animals. Furthermore, a recent study demonstrated rescue of neonatal MoBr/y mice following lateral ventricle injections of adeno-associated virus serotype 5 (AAV5) harboring a truncated ATP7A cDNA, in combination with copper treatment (Donsante et al., 2011). The authors proposed different effects of the two treatments: the copper injections increased the amount of brain copper available to levels that were 25–50% of the wild type, while the AAV5 gene delivery improved copper utilization. This was associated with enhanced activity of DBH and correction of brain pathology (Donsante et al., 2011). These findings further illustrate the critical role of copper and ATP7A for brain function and highlight the potential for gene therapy in the treatment of MD patients.
ATP7A-Related Motor Neuropathy
Recently, missense mutations in ATP7A were found to cause a form of dHMN (Kennerson et al., 2010; Yi et al., 2012), which represents the third clinical phenotype associated with mutations in ATP7A. dHMNs are a clinically and genetically heterogeneous group of diseases characterized by lower-motor neuron weakness and muscular atrophy (Rossor et al., 2012). Merner et al. (2010) proposed that a common factor in the disease mechanism may be altered copper homeostasis. The phenotype of ATP7A-related motor neuropathy is clinically distinct from that of MD, with variable age of onset that ranges from the first to the sixth decade of life, no overt abnormalities of copper metabolism, and typically distal muscle weakness and atrophy of the lower extremities leading to hand and foot deformities (Kaler, 2011). Nerve conduction studies suggest that the disease causes gradual degeneration of motor neuron axons in the limbs, beginning in the distal portion and progressing toward the cell body (Takata et al., 2004; Kennerson et al., 2009, 2010). The late-onset nature of the disease suggests that these mutations in ATP7A have subtle effects on ATP7A function that can take years to manifest clinically.
The missense mutations within ATP7A that result in T994I and P1386S substitutions were identified in two families with multiple affected males (Kennerson et al., 2010; Yi et al., 2012). These mutations are outside of the conserved functional domains and they cause abnormal ATP7A trafficking, affecting specifically motor neuron function. An abnormal interaction between ATP7A (T994I) and valosin-containing protein (p97/VCP) was demonstrated, the latter, an ATPase with functions that include vesicular trafficking and protein degradation by the ubiquitin (Ub)-proteasome system (UPS; Watts et al., 2004; Yi et al., 2012). Mutations in p97/VCP are also associated with other diseases that involve motor neuron degeneration (Watts et al., 2004). The significance of this interaction in mediating the disease phenotype awaits further investigation. Potential mechanisms that can lead to axonal degeneration as a result of these ATP7A mutations include copper deficiency, oxidative damage from mislocalized copper, and/or slowed synaptic copper release, resulting in inefficient down-regulation of the NMDA receptor and hence excitotoxicity leading to neuronal damage and axonal dieback.
In a significant proportion of WD patients, neurodegeneration and neurological presentation reveals an important role for ATP7B in maintaining neuronal copper homeostasis. WD manifests primarily in the liver and brain. Mutations that inactivate ATP7B lead to impaired biliary copper excretion (Terada et al., 1999) and consequently, hepatic copper overload, apoptotic cell death, liver damage, and spillage of copper into the plasma and CSF (Weisner et al., 1987; Kodama et al., 1988; Strand et al., 1998; Gitlin, 2003). Hence, copper also accumulates in extrahepatic tissues, notably the brain, kidneys, and cornea (Danks, 1995; Culotta and Gitlin, 2001).
Approximately 40–50% of WD cases present with neurological symptoms and these patients typically have a later onset than those with the liver disease, presenting in the second or third decade (Das and Ray, 2006; Gouider-Khouja, 2009). Although ATP7B is expressed in several brain regions, brain copper accumulation in WD appears to be secondary to the liver disease, because it can be reversed by transplantation (Emre et al., 2001; Schumacher et al., 2001). The psychiatric symptoms also are reversible with chelation therapy (Madsen and Gitlin, 2007). The main areas of the brain affected in WD patients include the thalamus, subthalamic nuclei, brainstem, cerebellum, and frontal cortex (Das and Ray, 2006). The precise mechanisms mediating neuronal injury in WD are not clear, but potentially involve increased extracellular copper combined with impaired copper homeostasis in those regions of the brain suffering loss of ATP7B function. For example, impaired DBH synthesis may explain the predominant abnormalities of the basal ganglia that result in Parkinsonian symptoms such as rigidity and tremor (Das and Ray, 2006; Pfeiffer, 2007).
The toxic milk mouse (tx) and the LEC rat are mouse models of WD that harbor a point mutation (Theophilos et al., 1996) or deletion (Wu et al., 1994), respectively, in Atp7b. Studies of the neurological symptoms and neurodegenerative processes in these models have been lacking until recently. One study found that despite an increase in brain copper levels of the tx mouse, there are no neurological or behavioral symptoms (Allen et al., 2006). In contrast, a more recent study reported copper deposition in the striatum and hippocampus of tx mice associated with an inflammatory response in these tissues, as well as motor and cognitive disturbances and impaired spatial memory (Terwel et al., 2011). The reason for the discrepancy between these two studies is not clear but may relate to the genetic background of the tx mice used.
Alzheimer’s disease is a progressive neurodegenerative disorder occurring late in life. Patients suffer memory loss and cognitive decline. Key pathological hallmarks include intra- and extracellular proteinaceous deposits (senile plaques comprising the Aβ peptides derived from the processing of APP and neurofibrillary tangles (NFTs) composed of hyperphosphorylated tau). The role of copper in AD is gaining prominence with the discoveries that: (i) it is increased and/or mis-localized in the AD brain; (ii) enriched in extracellular plaques; (iii) deficient in Aβ plaque neighboring brain regions; and (iv) disease-linked proteins, APP, Aβ, tau, and BACE1, are copper-binding proteins with key roles in brain metal regulation (reviewed in Kozlowski et al., 2009; Hung et al., 2010). These observations and findings of dysregulation of other metals such as iron and zinc have led to the “metal theory of AD” with the coining of the term, “metallostasis.” This represents the fatigue of brain metal regulation and distribution, leading to Aβ aggregation and deposition, intraneuronal iron accumulation, and consequently, oxidative injury and neurodegeneration (Roberts et al., 2012; Bush, 2013).
Genetic analysis of AD patients and healthy controls uncovered ATP7B as a genetic risk factor for AD. A number of single nucleotide polymorphisms (SNPs) in ATP7B are associated with increased risk for AD (Bucossi et al., 2011, 2012; Squitti et al., 2013). These changes occur in either a MBD, the ATP-binding N-domain or transmembrane domains, which may negatively affect ATP7B function in relation to metal-binding, ATP hydrolysis or copper translocation across the membrane. SNPs in the transmembrane domains present the strongest association for AD risk (Squitti et al., 2013). These observations further support a crucial role for ATP7B in maintaining brain copper homeostasis and a potential role in AD pathogenesis. In contrast to these observations, transgenic APP mice (CRND8) that are homozygous for the txJ mutation, and therefore lacking a functional ATP7B protein, exhibit elevated brain copper levels, but a markedly reduced number of amyloid plaques and decreased plasma Aβ levels (Phinney et al., 2003). The authors postulated that the mechanism of this beneficial effect of the txJ mutation involves increased clearance of peripheral Aβ pools. Alternatively, elevated intracellular copper due to the txJ mutation may correct the copper-deficient phenotype of the CRND8 mice. The copper-induced retention of APP at the cell surface, leading to reduced Aβ production and interaction with copper in lipid rafts may explain the decrease in Aβ and amyloid plaques (Hung et al., 2009; Acevedo et al., 2011).
APOE and CLUSTERIN (APOJ) polymorphisms represent the strongest and third strongest genetic risk factors for AD, respectively (Bertram et al., 2007). The encoded proteins have long associations with AD (Mahley et al., 2006; Nuutinen et al., 2009; Yu and Tan, 2012). ApoE and clusterin are well-known for their function as secreted extracellular chaperones with key roles in lipid transport. They have neuroprotective functions, cooperatively regulating the deposition and clearance of Aβ (DeMattos et al., 2004; Wilson et al., 2008). In humans, there are three common APOE alleles, ε2, ε3, and ε4. APOE-ε4 confers increased risk for AD. The presence of APOE-ε4 in WD patients with the common H1069Q mutation in ATP7B is associated with an earlier onset of symptoms (Litwin et al., 2012). In contrast, APOE-ε3 is associated with a significant delay in the onset of WD symptoms compared with APOE-ε4 carrying patients (Schiefermeier et al., 2000; Wang et al., 2003). This difference may be linked to the isoform-specific antioxidant activity of the ApoE isoforms (Miyata and Smith, 1996). ApoE4 is less effective than ApoE2/ApoE3 as an antioxidant, which may explain the greater susceptibility of ApoE4 patients to copper toxicity. While the exact mechanism remains unclear, these studies suggest a role for ApoE in copper regulation and in influencing WD phenotypes.
We recently demonstrated that clusterin interacts with ATP7A and ATP7B, and this interaction appears to facilitate the degradation of misfolded copper-ATPase molecules predominantly via the lysosome (Materia et al., 2011, 2012). Both MD and WD exhibit a high degree of clinical variability (de Bie et al., 2007; Tumer and Moller, 2009), with reports of identical mutations, even among siblings, conferring variable clinical expression (Duc et al., 1998; Borm et al., 2004). Hence, these observations implicate other factors in determining the clinical phenotype. Based on functional similarities between clusterin and ApoE, the association between ApoE isoforms and WD onset, and the role of clusterin in copper-ATPase degradation, these molecules potentially could play a role in modifying the expression of neurological disease such as AD, MD, and WD. Conceivably, genetic variations in the clusterin and ApoE alleles, together with environmental factors, could contribute to the variability in the clinical expression of MD and WD.
Prion diseases are characterized by the continual conformational change of the normal prion protein (PrPC) to an infectious, protease-resistant, β-sheet-rich form of the protein (PrPSc; Prusiner, 1982). The resultant toxic PrPSc aggregates can disrupt axonal transport and synaptic transmission and/or trigger apoptosis, leading to the neurodegenerative pathologies that are collectively termed transmissible spongiform encephalopathies (TSE) (reviewed in Davies and Brown, 2013).
Prion protein is a membrane glycoprotein with four N-terminal octameric repeats and a nearby site that binds copper (Hornshaw et al., 1995a,b; Brown et al., 1997). This protein is ubiquitously expressed but enriched in neurons and concentrated at the synapse (Sales et al., 1998). Its normal physiological role still remains to be fully elucidated but insight into the cell biology and biochemical properties of PrPC is revealing some clues regarding its function. Various studies have demonstrated that copper-binding induces PrPC internalization (Davies and Brown, 2013) prompting the suggestion that PrPC may be involved as a receptor for copper uptake or efflux (Brown and Harris, 2003). More recently, You et al. (2012) confirmed previous findings that copper modulates NMDA receptor activity. They further demonstrated that this occurs through a copper-dependent interaction between PrPC and the GluN1 subunit, which reduces glycine affinity for the receptor, thus suppressing its activity. The role of ATP7A-mediated synaptic copper release may be important in this context but whether it plays a direct role in PrPC-copper interactions is not clear.
In contrast to the beneficial role of copper in PrPC function noted above, other studies reported that copper binding to PrPC increases its conversion to PrPSc, and that copper chelation delays the onset of prion disease (Sigurdsson et al., 2003). In support of these studies, disruption of copper homeostasis due to a hypomorphic mutation in ATP7A delays the onset of prion disease in mice (Siggs et al., 2012). Copper levels in the brain are reduced by 60% and the amount of the disease-causing PrPSc is significantly lower than that of the controls. The controversies over the role of copper in PrPC function and prion disease remain to be clarified.
Copper plays a central role in a complex network of signaling pathways that regulate a host of physiological and pathophysiological processes. The crucial role of copper in brain and CNS development and function was highlighted three decades ago when the connection was made between infants with MD and copper deficiency (Danks et al., 1972). However, despite its importance, detailed knowledge of the mechanisms controlling brain copper homeostasis remains limited. Significant advances have been made with the subsequent discovery of key components of the copper regulatory network. The copper-ATPases, ATP7A and ATP7B are among these and since their discovery two decades ago, significant progress has been made toward understanding their pivotal role in normal copper homeostasis. Emerging data now reveal a complex and varied role for copper in the brain, and that the copper-ATPases are integral to the regulation and maintenance of copper-mediated processes within the brain. The consequences of their malfunction are clearly illustrated by the severe neurological deficits and neurodegeneration that accompany the disorders of copper transport, MD and WD. More subtle functional defects in the copper-ATPases or in factors that regulate their activity and/or stability are likely to contribute to other neurodegenerative diseases where copper is dysregulated, such as Alzheimer’s, motor neuron and prion diseases. Given the complexity of the CNS, much remains to be learned about the role of ATP7A and ATP7B in neurological development and neurodegenerative processes. Current ongoing research into the factors that affect the regulation of their expression, post-translational modification and activity will continue to provide new insights into their involvement and adaptive capacity during neuropathological processes associated with aging and disease.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This work was supported by funding from the National Health and Medical Research Council of Australia (Sharon La Fontaine). Jonathon Telianidis is supported by an Australian Postgraduate Award. The Florey Institute of Neuroscience and Mental Health acknowledges the strong support from the Victorian Government and in particular the funding from the Operational Infrastructure Support Grant.
- ^ http://asia.ensembl.org/Homo_sapiens/Gene/Summary?g=ENSG00000165240;r=X:77166194-77305892
- ^ http://asia.ensembl.org/Homo_sapiens/Gene/Summary?g=ENSG00000123191;r=13:52506809-52585630
Acevedo, K. M., Hung, Y. H., Dalziel, A. H., Li, Q. X., Laughton, K., Wikhe, K., et al. (2011). Copper promotes the trafficking of the amyloid precursor protein. J. Biol. Chem. 286, 8252–8262. doi: 10.1074/jbc.M110.128512
Achila, D., Banci, L., Bertini, I., Bunce, J., Ciofi-Baffoni, S., and Huffman, D. L. (2006). Structure of human Wilson protein domains 5 and 6 and their interplay with domain 4 and the copper chaperone HAH1 in copper uptake. Proc. Natl. Acad. Sci. U.S.A. 103, 5729–5734. doi: 10.1073/pnas.0504472103
Albrecht, P., Müller, A.-K., Ringelstein, M., Finis, D., Geerling, G., Cohn, E., et al. (2012). Retinal neurodegeneration in Wilson’s disease revealed by spectral domain optical coherence tomography. PLoS ONE 7:e49825. doi: 10.1371/journal.pone.0049825
Allen, K., Buck, N., Cheah, D., Gazeas, S., Bhathal, P., and Mercer, J. (2006). Chronological changes in tissue copper, zinc and iron in the toxic milk mouse and effects of copper loading. Biometals 19, 555–564. doi: 10.1007/s10534-005-5918-5
Aon-Bertolino, M. L., Romero, J. I., Galeano, P., Holubiec, M., Badorrey, M. S., Saraceno, G. E., et al. (2011). Thioredoxin and glutaredoxin system proteins-immunolocalization in the rat central nervous system. Biochim. Biophys. Acta 1810, 93–110. doi: 10.1016/j.bbagen.2010.06.011
Balijepalli, S., Tirumalai, P. S., Swamy, K. V., Boyd, M. R., Mieyal, J. J., and Ravindranath, V. (1999). Rat brain thioltransferase: regional distribution, immunological characterization, and localization by fluorescent in situ hybridization. J. Neurochem. 72, 1170–1178. doi: 10.1046/j.1471-4159.1999.0721170.x
Barnea, A., Hartter, D., Cho, G., Bhasker, K., Katz, B., and Edwards, M. (1990). Further characterization of the process of in vitro uptake of radiolabeled copper by the rat brain. J. Inorg. Biochem. 40, 103–110. doi: 10.1016/0162-0134(90)80043-W
Barnes, N., Tsivkovskii, R., Tsivkovskaia, N., and Lutsenko, S. (2005). The copper-transporting ATPases, Menkes and Wilson disease proteins, have distinct roles in adult and developing cerebellum. J. Biol. Chem. 280, 9640–9645. doi: 10.1074/jbc.M413840200
Barnes, N. L., Bartee, M., Y., Braiterman, L., Gupta, A., Ustiyan, V., Zuzel, V., et al. (2009). Cell-specific trafficking suggests a new role for renal ATP7B in the intracellular copper storage. Traffic 10, 767–779. doi: 10.1111/j.1600-0854.2009.00901.x
Bertram, L., Mcqueen, M. B., Mullin, K., Blacker, D., and Tanzi, R. E. (2007). Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database. Nat. Genet. 39, 17–23. doi: 10.1038/ng1934
Bohlken, A., Cheung, B. B., Bell, J. L., Koach, J., Smith, S., Sekyere, E., et al. (2009). ATP7A is a novel target of retinoic acid receptor [beta]2 in neuroblastoma cells. Br. J. Cancer 100, 96–105. doi: 10.1038/sj.bjc.6604833
Borm, B., Moller, L. B., Hausser, I., Emeis, M., Baerlocher, K., Horn, N., et al. (2004). Variable clinical expression of an identical mutation in the ATP7A gene for Menkes disease/occipital horn syndrome in three affected males in a single family. J. Pediatr. 145, 119–121. doi: 10.1016/j.jpeds.2004.04.033
Braiterman, L., Nyasae, L., Guo, Y., Bustos, R., Lutsenko, S., and Hubbard, A. (2009). Apical targeting and Golgi retention signals reside within a 9-amino acid sequence in the copper-ATPase, ATP7B. Am. J. Physiol. Gastrointest. Liver Physiol. 296, G433–G444. doi: 10.1152/ajpgi.90489.2008
Braiterman, L., Nyasae, L., Leves, F., and Hubbard, A. L. (2011). Critical roles for the COOH terminus of the Cu-ATPase ATP7B in protein stability, trans-Golgi network retention, copper sensing, and retrograde trafficking. Am. J. Physiol. Gastrointest. Liver Physiol. 301, G69–G81. doi: 10.1152/ajpgi.00038.2011
Brown, L. R., and Harris, D. A. (2003). Copper and zinc cause delivery of the prion protein from the plasma membrane to a subset of early endosomes and the Golgi. J. Neurochem. 87, 353–363. doi: 10.1046/j.1471-4159.2003.01996.x
Bucossi, S., Mariani, S., Ventriglia, M., Polimanti, R., Gennarelli, M., Bonvicini, C., et al. (2011). Association between the c. 2495 A>G ATP7B polymorphism and sporadic Alzheimer’s disease. Int. J. Alzheimers Dis. 2011, 973692. doi: 10.4061/2011/973692
Bucossi, S., Polimanti, R., Mariani, S., Ventriglia, M., Bonvicini, C., Migliore, S., et al. (2012). Association of K832R and R952K SNPs of Wilson’s disease gene with Alzheimer’s disease. J. Alzheimers Dis. 29, 913–919. doi: 10.3233/JAD-2012-111997
Buiakova, O. I., Xu, J., Lutsenko, S., Zeitlin, S., Das, K., Das, S., et al. (1999). Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation. Hum. Mol. Genet. 8, 1665–1671. doi: 10.1093/hmg/8.9.1665
Bull, P. C., Thomas, G. R., Rommens, J. M., Forbes, J. R., and Cox, D. C. (1993). The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nat. Genet. 5, 327–337 (Erratum in Nat. Genet. 1994, 6, 214). doi: 10.1038/ng1293-327
Burke, R., Commons, E., and Camakaris, J. (2008). Expression and localisation of the essential copper transporter DmATP7 in Drosophila neuronal and intestinal tissues. Int. J. Biochem. Cell Biol. 40, 1850–1860. doi: 10.1016/j.biocel.2008.01.021
Camakaris, J., Danks, D. M., Ackland, L., Cartwright, E., Borger, P., and Cotton, R. G. H. (1980). Altered copper metabolism in cultured cells from human Menkes’ syndrome and mottled mouse mutants. Biochem. Genet. 18, 117–131. doi: 10.1007/BF00504364
Cater, M. A., Forbes, J., La Fontaine, S., Cox, D., and Mercer, J. F. B. (2004). Intracellular trafficking of the human Wilson protein: the role of the six N-terminal metal binding sites. Biochem. J. 380(Pt 3), 805–813. doi: 10.1042/BJ20031804
Cater, M. A., La Fontaine, S., Deal, Y., Shield, K., and Mercer, J. F. B. (2006). ATP7B mediates vesicular sequestration of copper: insights into biliary copper excretion. Gastroenterology 130, 493–506. doi: 10.1053/j.gastro.2005.10.054
Cater, M. A., La Fontaine, S., and Mercer, J. F. (2007). Copper binding to the N-terminal metal binding sites or the CPC motif is not essential for copper-induced trafficking of the human Wilson protein (ATP7B). Biochem. J. 401, 143–153. doi: 10.1042/BJ20061055
Chelly, J., Tumer, Z., Tonnesen, T., Petterson, A., Ishikawa-Brush, Y., Tommerup, N., et al. (1993). Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein. Nat. Genet. 3, 14–19. doi: 10.1038/ng0193-14
Culotta, V. C., and Gitlin, J. D. (2001). “Disorders of copper transport,” in The Metabolic and Molecular Basis of Inherited Disease, 8th Edn, eds C. R. Scriver, A. L. Beaudet, W. S. Sly, and D. Valle (New York: McGraw-Hill), 3105–3126.
Danks, D. M. (1995). “Disorders of copper transport,” in The Metabolic and Molecular Basis of Inherited Disease, 7th Edn, eds C. R. Scriver, A. L. Beaudet, W. M. Sly, and D. Valle. (New York: McGraw-Hill), 2211–2235.
Davies, K. M., Hare, D. J., Cottam, V., Chen, N., Hilgers, L., Halliday, G., et al. (2013). Localization of copper and copper transporters in the human brain. Metallomics 5, 43–51. doi: 10.1039/c2mt20151h
de Bie, P., Muller, P., Wijmenga, C., and Klomp, L. W. (2007). Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes. J. Med. Genet. 44, 673–688. doi: 10.1136/jmg.2007.052746
de Bie, P., Vandesluis, B., Burstein, E., Berghe, P. V. E. V. D., Muller, P., Berger, R., et al. (2007). Distinct Wilson’s disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B. Gastroenterology 133, 1316–1326. doi: 10.1053/j.gastro.2007.07.020
DeMattos, R. B., Cirrito, J. R., Parsadanian, M., May, P. C., O’Dell, M. A., Taylor, J. W., et al. (2004). ApoE and clusterin cooperatively suppress A[beta] levels and deposition: evidence that ApoE regulates extracellular A[beta] metabolism in vivo. Neuron 41, 193–202. doi: 10.1016/S0896-6273(03)00850-X
Dierick, H. A., Adam, A. N., Escara-Wilke, J. F., and Glover, T. W. (1997). Immunocytochemical localization of the Menkes copper transport protein (ATP7A) to the trans Golgi network. Hum. Mol. Genet. 6, 409–416. doi: 10.1093/hmg/6.3.409
Donsante, A., Johnson, P., Jansen, L. A., and Kaler, S. G. (2010). Somatic mosaicism in Menkes disease suggests choroid plexus-mediated copper transport to the developing brain. Am. J. Med. Genet. A 152A, 2529–2534. doi: 10.1002/ajmg.a.33632
Donsante, A., Yi, L., Zerfas, P. M., Brinster, L. R., Sullivan, P., Goldstein, D. S., et al. (2011). ATP7A gene addition to the choroid plexus results in long-term rescue of the lethal copper transport defect in a Menkes disease mouse model. Mol. Ther. 19, 2114–2123. doi: 10.1038/mt.2011.143
Duc, H. H., Hefter, H., Stremmel, W., Castaneda-Guillot, C., Hernandez Hernandez, A., Cox, D. W., et al. (1998). His1069Gln and six novel Wilson disease mutations: analysis of relevance for early diagnosis and phenotype. Eur. J. Hum. Genet. 6, 616–623.
Ehrhart, J., Gluck, M., Mieyal, J., and Zeevalk, G. D. (2002). Functional glutaredoxin (thioltransferase) activity in rat brain and liver mitochondria. Parkinsonism Relat. Disord. 8, 395–400. doi: 10.1016/S1353-8020(02)00020-2
El Meskini, R., Cline, L. B., Eipper, B. A., and Ronnett, G. V. (2005). The developmentally regulated expression of Menkes protein ATP7A suggests a role in axon extension and synaptogenesis. Dev. Neurosci. 27, 333–348. doi: 10.1159/000086713
El Meskini, R., Crabtree, K. L., Cline, L. B., Mains, R. E., Eipper, B. A., and Ronnett, G. V. (2007). ATP7A (Menkes protein) functions in axonal targeting and synaptogenesis. Mol. Cell. Neurosci. 34, 409–421. doi: 10.1016/j.mcn.2006.11.018
El Meskini, R., Culotta, V. C., Mains, R. E., and Eipper, B. A. (2003). Supplying copper to the cuproenzyme peptidylglycine alpha-amidating monooxygenase. J. Biol. Chem. 278, 12278–12284. doi: 10.1074/jbc.M211413200
Emre, S., Atillasoy, E. O., Ozdemir, S., Schilsky, M., Rathna Varma, C. V., Thung, S. N., et al. (2001). Orthotopic liver transplantation for Wilson’s disease: a single-center experience. Transplantation 72, 1232–1236. doi: 10.1097/00007890-200110150-00008
Ferreira, R., Heckenlively, J. R., Menkes, J. H., and Bateman, B. (1998). Menkes disease. New ocular and electroretinographic findings. Ophthalmology 105, 1076–1078. doi: 10.1016/S0161-6420(98)96010-9
Francis, M. J., Jones, E. E., Levy, E. R., Ponnambalam, S., Chelly, J., and Monaco, A. P. (1998). A Golgi localization signal identified in the Menkes recombinant protein. Hum. Mol. Genet. 7, 1245–1252. doi: 10.1093/hmg/7.8.1245
Fujii, T., Ito, M., Tsuda, H., and Mikawa, H. (1990). Biochemical study on the critical period for treatment of the mottled brindled mouse. J. Neurochem. 55, 885–889. doi: 10.1111/j.1471-4159.1990.tb04574.x
Greenough, M., Pase, L., Voskoboinik, I., Petris, M. J., O’Brien, A. W., and Camakaris, J. (2004). Signals regulating trafficking of the Menkes (MNK; ATP7A) copper translocating P-type ATPase in polarized MDCK cells. Am. J. Physiol. Cell Physiol. 287, C1463–C1471. doi: 10.1152/ajpcell.00179.2004
Grimes, A., Hearn, C. J., Lockhart, P., Newgreen, D. F., and Mercer, J. F. B. (1997). Molecular basis of the brindled mouse mutant (Mobr): a murine model of Menkes disease. Hum. Mol. Genet. 6, 1037–1042. doi: 10.1093/hmg/6.7.1037
Guo, Y., Nyasae, L., Braiterman, L. T., and Hubbard, A. L. (2005). NH2-terminal signals in ATP7B Cu-ATPase mediate its Cu-dependent anterograde traffic in polarized hepatic cells. Am. J. Physiol. Gastrointest. Liver Physiol. 289, 904–916. doi: 10.1152/ajpgi.00262.2005
Hamza, I., Faisst, A., Prohaska, J., Chen, J., Gruss, P., and Gitlin, J. D. (2001). The metallochaperone Atox1 plays a critical role in perinatal copper homeostasis. Proc. Natl. Acad. Sci. U.S.A. 98, 6848–6852. doi: 10.1073/pnas.111058498
Hamza, I., Prohaska, J., and Gitlin, J. D. (2003). Essential role for Atox1 in the copper-mediated intracellular trafficking of the Menkes ATPase. Proc. Natl. Acad. Sci. U.S.A. 100, 1215–1220. doi: 10.1073/pnas.0336230100
Hamza, I., Schaefer, M., Klomp, L. W. J., and Gitlin, J. (1999). Interaction of the copper chaperone HAH1 with the Wilson disease protein is essential for copper homeostasis. Proc. Natl. Acad. Sci. U.S.A. 96, 13363–13368. doi: 10.1073/pnas.96.23.13363
Hopt, A., Korte, S., Fink, H., Panne, U., Niessner, R., Jahn, R., et al. (2003). Methods for studying synaptosomal copper release. J. Neurosci. Methods 128, 159–172. doi: 10.1016/S0165-0270(03)00173-0
Hornshaw, M. P., Mcdermott, J. R., and Candy, J. M. (1995a). Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein. Biochem. Biophys. Res. Commun. 207, 621–629. doi: 10.1006/bbrc.1995.1233
Hornshaw, M. P., Mcdermott, J. R., Candy, J. M., and Lakey, J. H. (1995b). Copper binding to the N-terminal tandem repeat region of mammalian and avian prion protein: structural studies using synthetic peptides. Biochem. Biophys. Res. Commun. 214, 993–999. doi: 10.1006/bbrc.1995.2384
Hung, I. H., Suzuki, M., Yamaguchi, Y., Yuan, D. S., Klausner, R. D., and Gitlin, J. D. (1997). Biochemical characterization of the Wilson disease protein and functional expression in the yeast Saccharomyces cerevisiae. J. Biol. Chem. 272, 21461–21466. doi: 10.1074/jbc.272.34.21461
Hung, Y. H., Layton, M. J., Voskoboinik, I., Mercer, J. F., and Camakaris, J. (2007). Purification and membrane reconstitution of catalytically active Menkes copper-transporting P-type ATPase (MNK; ATP7A). Biochem. J. 401, 569–579. doi: 10.1042/BJ20060924
Hung, Y. H., Robb, E. L., Volitakis, I., Ho, M., Evin, G., Li, Q. X., et al. (2009). Paradoxical condensation of copper with elevated beta-amyloid in lipid rafts under cellular copper deficiency conditions: implications for Alzheimer disease. J. Biol. Chem. 284, 21899–21907. doi: 10.1074/jbc.M109.019521
Huster, D., Hoppert, M., Lutsenko, S., Zinke, J., Lehmann, C., Mossner, J., et al. (2003). Defective cellular localization of mutant ATP7B in Wilson’s disease patients and hepatoma cell lines. Gastroenterology 124, 335–345. doi: 10.1053/gast.2003.50066
Iwase, T., Nishimura, M., Sugimura, H., Igarashi, H., Ozawa, F., Shinmura, K., et al. (1996). Localization of Menkes gene expression in the mouse brain; its association with neurological manifestations in Menkes model mice. Acta Neuropathol. 91, 482–488. doi: 10.1007/s004010050455
Kaler, S. G., Gallo, L. K., Proud, V. K., Percy, A. K., Mark, Y., Segal, N. A., et al. (1994). Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus. Nat. Genet. 8, 195–202. doi: 10.1038/ng1094-195
Kaler, S. G., Holmes, C. S., Goldstein, D. S., Tang, J., Godwin, S. C., Donsante, A., et al. (2008). Neonatal diagnosis and treatment of Menkes disease. N. Engl. J. Med. 358, 605–614. doi: 10.1056/NEJMoa070613
Kaler, S. G., and Schwartz, J. P. (1998). Expression of the Menkes disease homolog in rodent neuroglial cells. Neurosci. Res. Commun. 23, 61–66. doi: 10.1002/(SICI)1520-6769(199807/08)23:1<61::AID-NRC7>3.0.CO;2-J
Kardos, J., Kovacs, I., Hajos, F., Kalman, M., and Simonyi, M. (1989). Nerve endings from rat brain tissue release copper upon depolarization. A possible role in regulating neuronal excitability. Neurosci. Lett. 103, 139–144. doi: 10.1016/0304-3940(89)90565-X
Ke, B.-X., Llanos, R. M., Wright, M., Deal, Y., and Mercer, J. F. B. (2006). Alteration of copper physiology in mice overexpressing the human Menkes protein ATP7A. Am. J. Physiol. Regul. Integr. Comp. Physiol. 290, R1460–R1467. doi: 10.1152/ajpregu.00806.2005
Kennerson, M., Nicholson, G., Kowalski, B., Krajewski, K., El-Khechen, D., Feely, S., et al. (2009). X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21. Neurology 72, 246–252. doi: 10.1212/01.wnl.0000339483.86094.a5
Kennerson, M. L., Nicholson, G. A., Kaler, S. G., Kowalski, B., Mercer, J. F. B., Tang, J., et al. (2010). Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy. Am. J. Hum. Genet. 86, 343–352. doi: 10.1016/j.ajhg.2010.01.027
Ko, J. H., Son, W., Bae, G. Y., Kang, J. H., Oh, W., and Yoo, O. J. (2006). A new hepatocytic isoform of PLZF lacking the BTB domain interacts with ATP7B, the Wilson disease protein, and positively regulates ERK signal transduction. J. Cell Biochem. 99, 719–734. doi: 10.1002/jcb.20980
Kodama, H., Meguro, Y., Abe, T., Rayner, M. H., Suzuki, K. T., Kobayashi, S., et al. (1991). Genetic expression of Menkes disease in cultured astrocytes of the macular mouse. J. Inherit. Metab. Dis. 14, 896–901. doi: 10.1007/BF01800470
Kodama, H., Okabe, I., Yanagisawa, M., Nomiyama, H., Nomiyama, K., Nose, O., et al. (1988). Does CSF copper level in Wilson disease reflect copper accumulation in the brain? Pediatr. Neurol. 4, 35–37. doi: 10.1016/0887-8994(88)90022-7
Kozlowski, H., Janicka-Klos, A., Brasun, J., Gaggelli, E., Valensin, D., and Valensin, G. (2009). Copper, iron, and zinc ions homeostasis and their role in neurodegenerative disorders (metal uptake, transport, distribution and regulation). Coord. Chem. Rev. 253, 2665–2685. doi: 10.1016/j.ccr.2009.05.011
Krajacic, P., Qian, Y., Hahn, P., Dentchev, T., Lukinova, N., and Dunaief, J. L. (2006). Retinal localization and copper-dependent relocalization of the Wilson and Menkes disease proteins. Invest. Ophthalmol. Vis. Sci. 47, 3129–3134. doi: 10.1167/iovs.05-1601
Kuivaniemi, H., Peltonen, L., and Kivirikko, K. I. (1985). Type IX Ehlers-Danlos syndrome and Menkes syndrome: the decrease in lysyl oxidase activity is associated with a corresponding deficiency in the enzyme protein. Am. J. Hum. Genet. 37, 798–808.
Kumode, M., Yamano, T., and Shimada, M. (1994). Histochemical study of mitochondrial enzymes in cerebellar cortex of macular mutant mouse, a model of Menkes kinky hair disease. Acta Neuropath. 87, 313–316. doi: 10.1007/BF00296748
Kuo, Y.-M., Gitschier, J., and Packman, S. (1997). Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transporters. Hum. Mol. Genet. 6, 1043–1049. doi: 10.1093/hmg/6.7.1043
Kuo, Y. M., Gybina, A. A., Pyatskowit, J. W., Gitschier, J., and Prohaska, J. R. (2006). Copper transport protein (Ctr1) levels in mice are tissue specific and dependent on copper status. J. Nutr. 136, 21–26.
La Fontaine, S., Ackland, M. L., and Mercer, J. F. B. (2010). Mammalian copper-transporting P-type ATPases, ATP7A and ATP7B: emerging roles. Int. J. Biochem. Cell Biol. 42, 206–209. doi: 10.1016/j.biocel.2009.11.007
La Fontaine, S., Firth, S. D., Camakaris, J., Englezou, A., Theophilos, M. B., Petris, M. J., et al. (1998a). Correction of the copper transport defect of Menkes patient fibroblasts by expression of the Menkes and Wilson ATPases. J. Biol. Chem. 273, 31375–31380. doi: 10.1074/jbc.273.47.31375
La Fontaine, S., Firth, S. D., Lockhart, P. J., Brooks, H., Parton, R. G., Camakaris, J., et al. (1998b). Functional analysis and intracellular localization of the human Menkes protein (MNK) stably expressed from a cDNA construct in Chinese Hamster Ovary cells (CHO-K1). Hum. Mol. Genet. 7, 1293–1300. doi: 10.1093/hmg/7.8.1293
La Fontaine, S., Firth, S. D., Lockhart, P. J., Brooks, H., Camakaris, J., and Mercer, J. F. B. (1999). Intracellular localization and loss of copper-responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Moblo) and brindled (Mobr) mouse mutants. Hum. Mol. Genet. 8, 1069–1075. doi: 10.1093/hmg/8.6.1069
La Fontaine, S., Theophilos, M. B., Firth, S. D., Gould, R., Parton, R. G., and Mercer, J. F. B. (2001). Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPase. Hum. Mol. Genet. 10, 361–370. doi: 10.1093/hmg/10.4.361
Larin, D., Mekios, C., Das, K., Ross, B., An-Suei, Y., and Gilliam, T. C. (1999). Characterization of the interaction between the Wilson and Menkes disease proteins and the cytoplasmic copper chaperone, HAH1P. J. Biol. Chem. 274, 28497–28504. doi: 10.1074/jbc.274.40.28497
Levinson, B., Vulpe, C., Elder, B., Martin, C., Verley, F., Packman, S., et al. (1994). The mottled gene is the mouse homologue of the Menkes disease gene. Nat. Genet. 6, 369–373. doi: 10.1038/ng0494-369
Li, X., Chen, S., Wang, Q., Zack, D. J., Snyder, S. H., and Borjigin, J. (1998). A pineal regulatory element (PIRE) mediates transactivation by the pineal/retina-specific transcription factor CRX. Proc. Natl. Acad. Sci. U.S.A. 95, 1876–1881. doi: 10.1073/pnas.95.4.1876
Lim, C. M., Cater, M. A., Mercer, J. F., and La Fontaine, S. (2006a). Copper-dependent interaction of glutaredoxin with the N termini of the copper-ATPases (ATP7A and ATP7B) defective in Menkes and Wilson diseases. Biochem. Biophys. Res. Commun. 348, 428–436. doi: 10.1016/j.bbrc.2006.07.067
Lim, C. M., Cater, M. A., Mercer, J. F. B., and La Fontaine, S. (2006b). Copper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7A. J. Biol. Chem. 281, 14006–14014. doi: 10.1074/jbc.M512745200
Linz, R., Barnes, N. L., Zimnicka, A. M., Kaplan, J. H., Eipper, B., and Lutsenko, S. (2008). Intracellular targeting of copper-transporting ATPase ATP7A in a normal and Atp7b -/- kidney. Am. J. Physiol. Renal. Physiol. 294, F53–F61. doi: 10.1152/ajprenal.00314.2007
Litwin, T., Gromadzka, G., and Czlonkowska, A. (2012). Apolipoprotein E gene (APOE) genotype in Wilson’s disease: impact on clinical presentation. Parkinsonism Relat. Disord. 18, 367–369. doi: 10.1016/j.parkreldis.2011.12.005
Liu, P.-C., Chen, Y.-W., Centeno, J., Quezado, M., Lem, K., and Kaler, S. (2005a). Downregulation of myelination, energy, and translational genes in Menkes disease brain. Mol. Genet. Metab. 85, 291–300. doi: 10.1016/j.ymgme.2005.04.007
Liu, T., Bohlken, A., Kuljaca, S., Lee, M., Nguyen, T., Smith, S., et al. (2005b). The retinoid anticancer signal: mechanisms of target gene regulation. Br. J. Cancer 93, 310–318. doi: 10.1038/sj.bjc.6602700
Llanos, R. M., Ke, B.-X., Wright, M., Deal, Y., Monty, F., Kramer, D. R., et al. (2006). Correction of a mouse model of Menkes disease by the human Menkes gene. Biochim. Biophys. Acta 1762, 485–493. doi: 10.1016/j.bbadis.2005.12.011
Madsen, E. C., Morcos, P. A., Mendelsohn, B. A., and Gitlin, J. D. (2008). In vivo correction of a Menkes disease model using antisense oligonucleotides. Proc. Natl. Acad. Sci. U.S.A. 105, 3909–3914. doi: 10.1073/pnas.0710865105
Mahley, R. W., Weisgraber, K. H., and Huang, Y. (2006). Apolipoprotein E4: a causative factor and therapeutic target in neuropathology, including Alzheimer’s disease. Proc. Natl. Acad. Sci. U.S.A. 103, 5644–5651. doi: 10.1073/pnas.0600549103
Materia, S., Cater, M. A., Klomp, L. W., Mercer, J. F., and La Fontaine, S. (2011). Clusterin (APOJ): a molecular chaperone that facilitates degradation of the copper-ATPases, ATP7A and ATP7B. J. Biol. Chem. 286, 10073–10083. doi: 10.1074/jbc.M110.190546
Materia, S., Cater, M. A., Klomp, L. W. J., Mercer, J. F. B., and La Fontaine, S. (2012). Clusterin and COMMD1 independently regulate degradation of the mammalian copper ATPases ATP7A and ATP7B. J. Biol. Chem. 287, 2485–2499. doi: 10.1074/jbc.M111.302216
Mendelsohn, B. A., Yin, C., Johnson, S. L., Wilm, T. P., Solnica-Krezel, L., and Gitlin, J. D. (2006). Atp7a determines a hierarchy of copper metabolism essential for notochord development. Cell Metab. 4, 155–162. doi: 10.1016/j.cmet.2006.05.001
Menkes, J. H., Alter, M., Steigleder, G. K., Weakley, D. R., and Sung, J. H. (1962). A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration. Pediatrics 29, 764–779.
Mercer, J. F. B., Grimes, A., Ambrosini, L., Lockhart, P., Paynter, J. A., Dierick, H., et al. (1994). Mutations in the murine homologue of the Menkes disease gene in dappled and blotchy mice. Nat. Genet. 6, 374–378. doi: 10.1038/ng0494-374
Mercer, J. F. B., Livingston, J., Hall, B. K., Paynter, J. A., Begy, C., Chandrasekharappa, S., et al. (1993). Isolation of a partial candidate gene for Menkes disease by positional cloning. Nat. Genet. 3, 20–25. doi: 10.1038/ng0193-20
Merner, N. D., Dion, P. A., and Rouleau, G. A. (2010). Recent advances in the genetics of distal hereditary motor neuropathy give insight to a disease mechanism involving copper homeostasis that may extend to other motor neuron disorders. Clin. Genet. 79, 23–34. doi: 10.1111/j.1399-0004.2010.01591.x
Michalczyk, A., Bastow, E., Greenough, M., Camakaris, J., Freestone, D., Taylor, P., et al. (2008). ATP7B expression in human breast epithelial cells is mediated by lactational hormones. J. Histochem. Cytochem. 56, 389–399. doi: 10.1369/jhc.7A7300.2008
Mieyal, J. J., Gallogly, M. M., Qanungo, S., Sabens, E. A., and Shelton, M. D. (2008). Molecular mechanisms and clinical implications of reversible protein S-glutathionylation. Antioxid. Redox Signal. 10, 1941–1988. doi: 10.1089/ars.2008.2089
Miyata, M., and Smith, J. D. (1996). Apolipoprotein E allele-specific antioxidant activity and effects on cytotoxicity by oxidative insults and [beta]-amyloid peptides. Nat. Genet. 14, 55–61. doi: 10.1038/ng0996-55
Monnot, A. D., Zheng, G., and Zheng, W. (2012). Mechanism of copper transport at the blood-cerebrospinal fluid barrier: influence of iron deficiency in an in vitro model. Exp. Biol. Med. (Maywood) 237, 327–333. doi: 10.1258/ebm.2011.011170
Monty, J.-F., Llanos, R. M., Mercer, J. F. B., and Kramer, D. R. (2005). Copper exposure induces trafficking of the Menkes protein in intestinal epithelium of ATP7A transgenic mice. J. Nutr. 135, 2762–2766.
Murata, Y., Kodama, H., Abe, T., Ishida, N., Nishimura, M., Levinson, B., et al. (1997). Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes disease. Pediatr. Res. 42, 436–442. doi: 10.1203/00006450-199710000-00003
Niciu, M. J., Ma, X. M., El Meskini, R., Pachter, J. S., Mains, R. E., and Eipper, B. A. (2007). Altered ATP7A expression and other compensatory responses in a murine model of Menkes disease. Neurobiol. Dis. 27, 278–291. doi: 10.1016/j.nbd.2007.05.004
Niciu, M. J., Ma, X.-M., El-Meskini, R., Ronnett, G. V., Mains, R. E., and Eipper, B. A. (2006). Developmental changes in the expression of ATP7A during a critical period in postnatal neurodevelopment. Neuroscience 139, 947–964. doi: 10.1016/j.neuroscience.2006.01.044
Norgate, M., Southon, A., Zou, S., Zhan, M., Sun, Y., Batterham, P., and Camakaris, J. (2007). Copper homeostasis gene discovery in Drosophila melanogaster. Biometals 20, 683–697. doi: 10.1007/s10534-006-9075-2
Nyasae, L., Bustos, R., Braiterman, L., Eipper, B., and Hubbard, A. (2007). Dynamics of endogenous ATP7A (Menkes protein) in intestinal epithelial cells: copper-dependent redistribution between two intracellular sites. Am. J. Physiol. Gastrointest. Liver Physiol. 292, G1181–G1194. doi: 10.1152/ajpgi.00472.2006
Okabe, M., Saito, S., Saito, T., Ito, K., Kimura, S., Niioka, T., et al. (1998). Histochemical localization of superoxide dismutase activity in rat brain. Free Radic. Biol. Med. 24, 1470–1476. doi: 10.1016/S0891-5849(98)00013-6
Okeda, R., Gei, S., Chen, I., Okaniwa, M., Shinomiya, M., and Matsubara, O. (1991). Menkes’ kinky hair disease: morphological and immunohistochemical comparison of two autopsied patients. Acta Neuropathol. (Berl.) 81, 450–457. doi: 10.1007/BF00293467
Petris, M. J., Camakaris, J., Greenough, M., La Fontaine, S., and Mercer, J. F. B. (1998). A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network. Hum. Mol. Genet. 7, 2063–2071. doi: 10.1093/hmg/7.13.2063
Petris, M. J., and Mercer, J. F. B. (1999). The Menkes protein (ATP7A; MNK) cylces via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal. Hum. Mol. Genet. 8, 2107–2115. doi: 10.1093/hmg/8.11.2107
Petris, M. J., Mercer, J. F. B., Culvenor, J. G., Lockhart, P., Gleeson, P. A., and Camakaris, J. (1996). Ligand-regulated transport of the Menkes copper P-type ATPase efflux pump from the Golgi apparatus to the plasma membrane: a novel mechanism of regulated trafficking. EMBO J. 15, 6084–6095.
Petris, M. J., Voskoboinik, I., Cater, M., Smith, K., Kim, B. E., Llanos, R. M., et al. (2002). Copper-regulated trafficking of the Menkes disease copper ATPase is associated with formation of a phosphorylated catalytic intermediate. J. Biol. Chem. 277, 46736–46742. doi: 10.1074/jbc.M208864200
Petrukhin, K., Fischer, S. G., Pirastu, M., Tanzi, R. E., Chernov, I., Devoto, M., et al. (1993). Mapping, cloning ang genetic characterization of the region containing the Wilson disease gene. Nat. Genet. 5, 338–343. doi: 10.1038/ng1293-338
Phinney, A., Drisaldi, B., Sd Schmidt, A., Lugowski, S., Coronado, V., Liang, Y., et al. (2003). In vivo reduction of amyloid-beta by a mutant copper transporter. Proc. Natl. Acad. Sci. U.S.A. 100, 14193–14198. doi: 10.1073/pnas.2332851100
Qi, M., and Byers, P. H. (1998). Constitutive skipping of alternatively spliced exon 10 in the ATP7A gene abolishes Golgi localization of the Menkes protein and produces the occipital horn syndrome. Hum. Mol. Genet. 7, 465–469. doi: 10.1093/hmg/7.3.465
Qian, Y., Tiffany-Castiglioni, E., and Harris, E. D. (1997). A Menkes P-type ATPase involved in copper homeostasis in the central nervous system of the rat. Brain Res. Mol. Brain Res. 48, 60–66. doi: 10.1016/S0169-328X(97)00083-1
Qin, Z., Itoh, S., Jeney, V., Ushio-Fukai, M., and Fukai, T. (2005). Essential role for the Menkes ATPase in activation of extracellular superoxide dismutase: implication for vascular oxidative stress. FASEB J. 334–336. doi: 10.1096/fj.05-4564fje
Roberts, B. R., Ryan, T. M., Bush, A. I., Masters, C. L., and Duce, J. A. (2012). The role of metallobiology and amyloid-β peptides in Alzheimer’s disease. J. Neurochem. 120, 149–166. doi: 10.1111/j.1471-4159.2011.07500.x
Roelofsen, H., Wolters, H., Luyn, M. J. A. V., Miura, N., Kuipers, F., and Vonk, R. J. (2000). Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion. Gastroenterology 119, 782–793. doi: 10.1053/gast.2000.17834
Saito, T., Nagao, T., Okabe, M., and Saito, K. (1996). Neurochemical and histochemical evidence for an abnormal catecholamine metabolism in the cerebral cortex of the Long-Evans Cinnamon rat before excessive copper accumulation in the brain. Neurosci. Lett. 216, 195–198.
Saito, T., Okabe, M., Hosokawa, T., Kurasaki, M., Hata, A., Endo, F., et al. (1999). Immunohistochemical determination of the Wilson copper-transporting P-type ATPase in the brain tissues of the rat. Neurosci. Lett. 266, 13–16. doi: 10.1016/S0304-3940(99)00258-X
Sales, N., Rodolfo, K., Hassig, R., Faucheux, B., Di Giamberardino, L., and Moya, K. L. (1998). Cellular prion protein localization in rodent and primate brain. Eur. J. Neurosci. 10, 2464–2471. doi: 10.1046/j.1460-9568.1998.00258.x
Scheiber, I., Dringen, R., and Mercer, J. F. B. (2013). “Copper: effects of deficiency and overload,” in Interrelations between Essential Metal Ions and Human Diseases, eds A. Sigel, H. Sigel, and R. K. O. Sigel (Dordrecht: Springer) (in press).
Schiefermeier, M., Kollegger, H., Madl, C., Polli, C., Oder, W., Kuhn, H., et al. (2000). The impact of apolipoprotein E genotypes on age at onset of symptoms and phenotypic expression in Wilson’s disease. Brain 123(Pt 3), 585–590. doi: 10.1093/brain/123.3.585
Schlief, M. L., West, T., Craig, A. M., Holtzman, D. M., and Gitlin, J. D. (2006). Role of the Menkes copper-transporting ATPase in NMDA receptor-mediated neuronal toxicity. Proc. Natl. Acad. Sci. U.S.A. 103, 14919–14924. doi: 10.1073/pnas.0605390103
Schumacher, G., Platz, K. P., Mueller, A. R., Neuhaus, R., Luck, W., Langrehr, J. M., et al. (2001). Liver transplantation in neurologic Wilson’s disease. Transplant. Proc. 33, 1518–1519. doi: 10.1016/S0041-1345(00)02578-1
Setty, S. R. G., Tenza, D., Sviderskaya, E. V., Bennett, D. C., Raposo, G., and Marks, M. S. (2008). Cell-specific ATP7A transport sustains copper-dependent tyrosinase activity in melanosomes. Nature 454, 1142–1146. doi: 10.1038/nature07163
Siggs, O. M., Cruite, J. T., Du, X., Rutschmann, S., Masliah, E., Beutler, B., et al. (2012). Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease. Proc. Natl. Acad. Sci. U.S.A. 109, 13733–13738. doi: 10.1073/pnas.1211499109
Sigurdsson, E. M., Brown, D. R., Alim, M. A., Scholtzova, H., Carp, R., Meeker, H. C., et al. (2003). Copper chelation delays the onset of prion disease. J. Biol. Chem. 278, 46199–46202. doi: 10.1074/jbc.C300303200
Singleton, W. C., Mcinnes, K. T., Cater, M. A., Winnall, W. R., Mckirdy, R., Yu, Y., et al. (2010). Role of glutaredoxin1 and glutathione in regulating the activity of the copper-transporting P-type ATPases, ATP7A and ATP7B. J. Biol. Chem. 285, 27111–27121. doi: 10.1074/jbc.M110.154468
Squitti, R., Polimanti, R., Bucossi, S., Ventriglia, M., Mariani, S., Manfellotto, D., et al. (2013). Linkage disequilibrium and haplotype analysis of the ATP7B gene in Alzheimer’s disease. Rejuvenation Res. 16, 3–10. doi: 10.1089/rej.2012.1357
Stephenson, S. E. M., Dubach, D., Lim, C. M., Mercer, J. F. B., and La Fontaine, S. (2005). A single PDZ domain protein interacts with the Menkes copper ATPase, ATP7A: a new protein implicated in copper homeostasis. J. Biol. Chem. 280, 33270–33279. doi: 10.1074/jbc.M505889200
Steveson, T. C., Ciccotosto, D. D., Ma, X.-M., Mueller, G. P., Mains, R. E., and Eipper, B. A. (2003). Menkes protein contirbutes to the function of peptidylglycine a-amidating monooxygenase. Endocrinology 144, 188–200. doi: 10.1210/en.2002-220716
Strand, S., Hofmann, W. J., Grambihler, A., Hug, H., Volkmann, M., Otto, G., et al. (1998). Hepatic failure and liver cell damage in acute Wilson’s disease involve CD95 (APO-1/Fas) mediated apoptosis. Nat. Med. 4, 588–593. doi: 10.1038/nm0598-588
Strausak, D., Howie, M. K., Firth, S. D., Schlicksupp, A., Pipkorn, R., Multhaup, G., et al. (2003). Kinetic analysis of the interaction of the copper chaperone Atox1 with the metal binding sites of the Menkes protein. J. Biol. Chem. 278, 20821–20827. doi: 10.1074/jbc.M212437200
Strausak, D., La Fontaine, S., Hill, J., Firth, S. D., Lockhart, P. J., and Mercer, J. F. B. (1999). The role of GMXCXXC metal binding sites in the copper-induced redistribution of the Menkes protein. J. Biol. Chem. 274, 11170–11177. doi: 10.1074/jbc.274.16.11170
Takata, R. I., Speck Martins, C. E., Passosbueno, M. R., Abe, K. T., Nishimura, A. L., Da Silva, M. D., et al. (2004). A new locus for recessive distal spinal muscular atrophy at Xq13.1-q21. J. Med. Genet. 41, 224–229. doi: 10.1136/jmg.2003.013201
Tang, J., Donsante, A., Desai, V., Patronas, N., and Kaler, S. G. (2008). Clinical outcomes in Menkes disease patients with a copper-responsive ATP7A mutation, G727R. Mol. Genet. Metab. 95, 174–181. doi: 10.1016/j.ymgme.2008.06.015
Tanzi, R. E., Petrukhin, K., Chernov, I., Pellequer, J. L., Wasco, W., Ross, B., et al. (1993). The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Nat. Genet. 5, 344–350. doi: 10.1038/ng1293-344
Tchaparian, E. H., Uriu-Adams, J. Y., Keen, C. L., Mitchell, A. E., and Rucker, R. B. (2000). Lysyl oxidase and P-ATPase-7A expression during embryonic development in the rat. Arch. Biochem. Biophys. 379, 71–77. doi: 10.1006/abbi.2000.1842
Terada, K., Aiba, N., Yang, X.-L., Iida, M., Nakai, M., Miura, N., et al. (1999). Biliary excretion of copper in LEC rat after introduction of copper transporting P-type ATPase, ATP7B. FEBS Lett. 448, 53–56. doi: 10.1016/S0014-5793(99)00319-1
Terada, K., Nakako, T., Yang, X.-L., Iida, M., Aiba, N., Minamiya, Y., et al. (1998). Restoration of holoceruloplasmin synthesis in LEC rat after infusion of recombinant adenovirus bearing WND cDNA. J. Biol. Chem. 273, 1815–1820. doi: 10.1074/jbc.273.3.1815
Terwel, D., Loschmann, Y. N., Schmidt, H. H., Scholer, H. R., Cantz, T., and Heneka, M. T. (2011). Neuroinflammatory and behavioural changes in the Atp7B mutant mouse model of Wilson’s disease. J. Neurochem. 118, 105–112. doi: 10.1111/j.1471-4159.2011.07278.x
Tiffany-Castiglioni, E., Hong, S., and Qian, Y. (2011). Copper handling by astrocytes: insights into neurodegenerative diseases. Int. J. Dev. Neurosci. 29, 811–818. doi: 10.1016/j.ijdevneu.2011.09.004
Tsivkovskii, R., Eisses, J. F., Kaplan, J. H., and Lutsenko, S. (2002). Functional properties of the copper-transporting ATPase ATP7B (the Wilson’s disease protein) expressed in insect cells. J. Biol. Chem. 277, 976–983. doi: 10.1074/jbc.M109368200
Vanderwerf, S. M., Cooper, M. J., Stetsenko, I. V., and Lutsenko, S. (2001). Copper specifically regulates intracellular phosphorylation of the Wilson’s disease protein, a human copper-transporting ATPase. J. Biol. Chem. 276, 36289–36294. doi: 10.1074/jbc.M102055200
Veldhuis, N., Gaeth, A., Pearson, R., Gabriel, K., and Camakaris, J. (2009a). The multi-layered regulation of copper translocating P-type ATPases. Biometals 22, 177–190. doi: 10.1007/s10534-008-9183-2
Veldhuis, N. A., Valova, V. A., Gaeth, A. P., Palstra, N., Hannan, K. M., Michell, B. J., et al. (2009b). Phosphorylation regulates copper-responsive trafficking of the Menkes copper transporting P-type ATPase. Int. J. Biochem. Cell Biol. 41, 2403–2412. doi: 10.1016/j.biocel.2009.06.008
Voskoboinik, I., Brooks, H., Smith, S., Shen, P., and Camakaris, J. (1998). ATP-dependent copper transport by the Menkes protein in membrane vesicles isolated from cultured Chinese hamster ovary cells. FEBS Lett. 438, 178–182. doi: 10.1016/S0014-5793(98)01059-X
Voskoboinik, I., Fernando, R., Veldhuis, N., Hannan, K. M., Marmy-Conus, N., Pearson, R. B., et al. (2003). Protein kinase-dependent phosphorylation of the Menkes copper P-type ATPase. Biochem. Biophys. Res. Commun. 303, 337–342. doi: 10.1016/S0006-291X(03)00329-2
Voskoboinik, I., Greenough, M., La Fontaine, S., Mercer, J. F. B., and Camakaris, J. (2001a). Functional studies on the Wilson copper P-type ATPase and toxic milk mouse mutant. Biochem. Biophys. Res. Comm. 281, 966–970. doi: 10.1006/bbrc.2001.4445
Voskoboinik, I., Mar, J., Strausak, D., and Camakaris, J. (2001b). The regulation of catalytic activity of the menkes copper-translocating P-type ATPase. Role of high affinity copper-binding sites. J. Biol. Chem. 276, 28620–28627. doi: 10.1074/jbc.M103532200
Vulpe, C., Levinson, B., Whitney, S., Packman, S., and Gitschier, J. (1993). Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase. Nat. Genet. 3, 7–13. doi: 10.1038/ng0193-7
Walker, J. M., Huster, D., Ralle, M., Morgan, C. T., Blackburn, N. J., and Lutsenko, S. (2004). The N-terminal metal-binding site 2 of the Wilson’s Disease Protein plays a key role in the transfer of copper from Atox1. J. Biol. Chem. 279, 15376–15384. doi: 10.1074/jbc.M400053200
Watts, G. D., Wymer, J., Kovach, M. J., Mehta, S. G., Mumm, S., Darvish, D., et al. (2004). Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. Nat. Genet. 36, 377–381. doi: 10.1038/ng1332
Weisner, B., Hartard, C., and Dieu, C. (1987). CSF copper concentration: a new parameter for diagnosis and monitoring therapy of Wilson’s disease with cerebral manifestation. J. Neurol. Sci. 79, 229–237. doi: 10.1016/0022-510X(87)90275-9
White, C., Kambe, T., Fulcher, Y. G., Sachdev, S. W., Bush, A. I., Fritsche, K., et al. (2009). Copper transport into the secretory pathway is regulated by oxygen in macrophages. J. Cell Sci. 122, 1315–1321. doi: 10.1242/jcs.043216
Wilson, M. R., Yerbury, J. J., and Poon, S. (2008). Potential roles of abundant extracellular chaperones in the control of amyloid formation and toxicity. Mol. Biosyst. 4, 42–52. doi: 10.1039/b712728f
Wu, J., Forbes, J. R., Chen, H. S., and Cox, D. W. (1994). The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene. Nat. Genet. 7, 541–544. doi: 10.1038/ng0894-541
Yamaguchi, Y., Heiny, M. E., and Gitlin, J. D. (1993). Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease. Biochem. Biophys. Res. Comm. 197, 271–277. doi: 10.1006/bbrc.1993.2471
Yamaguchi, Y., Heiny, M. E., Suzuki, M., and Gitlin, J. D. (1996). Biochemical characterization and intracellular localization of the Menkes disease protein. Proc. Natl. Acad. Sci. U.S.A. 93, 14030–14035. doi: 10.1073/pnas.93.24.14030
Yang, X.-L., Miura, N., Kawarada, Y., Terada, K., Petrukhin, K., Gilliam, T. C., et al. (1997). Two forms of Wilson disease protein produced by alternative splicing are localized in distinct cellular compartments. Biochem. J. 326, 897–902.
Yi, L., Donsante, A., Kennerson, M. L., Mercer, J. F., Garbern, J. Y., and Kaler, S. G. (2012). Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathy. Hum. Mol. Genet. 21, 1794–1807. doi: 10.1093/hmg/ddr612
You, H., Tsutsui, S., Hameed, S., Kannanayakal, T. J., Chen, L., Xia, P., et al. (2012). Abeta neurotoxicity depends on interactions between copper ions, prion protein, and N-methyl-D-aspartate receptors. Proc. Natl. Acad. Sci. U.S.A. 109, 1737–1742. doi: 10.1073/pnas.1110789109
Keywords: copper, copper homeostasis, ATP7A, ATP7B, Menkes disease, Wilson disease, occipital horn syndrome, ATP7A-related motor neuropathy
Citation: Telianidis J, Hung YH, Materia S and La Fontaine S (2013) Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis. Front. Aging Neurosci. 5:44. doi: 10.3389/fnagi.2013.00044
Received: 06 May 2013; Paper pending published: 14 June 2013;
Accepted: 05 August 2013; Published online: 23 August 2013.
Edited by:Anthony Robert White, The University of Melbourne, Australia
Reviewed by:Anthony Robert White, The University of Melbourne, Australia
Katherine Price, Icahn School of Medicine at Mount Sinai, USA
Copyright © 2013 Telianidis, Hung, Materia and La Fontaine. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Sharon La Fontaine, Centre for Cellular and Molecular Biology, School of Life and Environmental Sciences, Deakin University, Melbourne Campus, 221 Burwood Highway, Burwood, VIC 3125, Australia e-mail: email@example.com
†Present address: Jonathon Telianidis, Department of Physiology, Monash University, Clayton, VIC, Australia