Abstract
The retinal pigment epithelium (RPE) is a uniquely polarized epithelium that lies adjacent to the photoreceptor cells in the retina, and is essential for photoreceptor function and viability. Two major motile organelles present in the RPE are the melanosomes, which are important for absorbing stray light, and phagosomes that result from the phagocytosis of the distal tips of the photoreceptor cilium, known as the photoreceptor outer segment (POS). These organelles are transported along microtubules, aligned with the apical-basal axis of the RPE. Although they undergo a directional migration, the organelles exhibit bidirectional movements, indicating both kinesin and dynein motor function in their transport. Apical melanosome localization requires dynein; it has been suggested that kinesin contribution might be complex with the involvement of more than one type of kinesin. POS phagosomes undergo bidirectional movements; roles of both plus- and minus-end directed motors appear to be important in the efficient degradation of phagosomes. This function is directly related to retinal health, with defects in motor proteins, or in the association of the phagosomes with the motors, resulting in retinal degenerative pathologies.
Introduction
Motor-dependent intracellular transport is an essential process for all eukaryotic cells. It underlies numerous critical functions, including the trafficking and positioning of organelles, the endo- and exocytosis of biological molecules, the establishment of polarized domains, and the translocation of chromosomes during cell division. Impaired motor-dependent trafficking is at the root etiology of several neuro-pathologies, lysosomal storage disorders, and ciliopathies. In vitro models well suited for the study of intracellular transport, and its disease-related mechanisms, include polarized cells, such as neurons and epithelial cells, in which specific cargos must be trafficked to distinct cellular compartments.
The retinal pigment epithelium (RPE) is a polarized monolayer of cells situated between the light-sensitive photoreceptor cells and the nutrient-rich choriocapillaris (Lakkaraju et al., 2020). These pigmented cells perform supportive functions that are vital to the health of photoreceptors and the retina as a whole. Functions include: 1) absorption of stray light, 2) transport of water, ions, nutrients, and waste products, 3) recycling of the visual chromophore, 4) secretion of growth and signaling factors, 5) phagocytosis of distal photoreceptor outer segment (POS) disk membranes, and 6) contribution to the metabolic ecosystem of the outer retina (Strauss, 2005; Lakkaraju et al., 2020). In the mouse retina, a single RPE cell serves up to 200 photoreceptor cells (Volland et al., 2015). RPE cells are postmitotic and must therefore perform these functions throughout the lifetime of the organism (Ts’o and Friedman, 1967). The supportive capability of the RPE in the retina is heavily dependent on its differentiated state (Zhao et al., 2011), which represents a highly specialized epithelium (Lakkaraju et al., 2020).
Studies of the properties of specialized cells, like the RPE, tell us about the generality of basic principles and adaptions of molecular mechanisms. In this Mini Review, we highlight the role molecular motor proteins play in facilitating the functions of polarized RPE cells. We focus on microtubule motor-driven motility of two major RPE organelles: melanosomes, which characterize the RPE in most animals, and phagosomes, which result from the daily ingestion of POS tips. We also discuss how defective microtubule motor transport may contribute to retinal pathologies that impair our sense of vision.
Organization of the Microtubule Cytoskeleton in the RPE
Cells have a cytoskeleton composed of microtubules, actin, and intermediate filaments, which maintain cell shape and organization. Of these cytoskeletal elements, the microtubules are the biggest; they are composed of a- and ß-tubulin monomers that form a hollow cylindrical polymer 25 nm in diameter (Akhmanova and Steinmetz, 2008). Microtubules are highly dynamic and polarized structures, with a plus-end that is fast growing and a minus-end that is slow growing (Mitchison and Kirschner, 1984). In a nonpolarized cell, the microtubule plus-end is directed towards the cell periphery while the minus-end is anchored at the microtubule-organizing center (MTOC) (Vorobjev and Nadezhdina, 1987). The MTOC is composed of the centrosome and surrounding pericentriolar material, and typically lies near the nucleus (Vorobjev and Nadezhdina, 1987). In contrast, polarized cells such as the RPE have an MTOC that has migrated away from the nucleus and towards the apical region of the cell (Bacallao et al., 1989; Bre et al., 1990). The microtubule organization of the RPE is similar to that reported for other confluent epithelial cells (Bacallao et al., 1989; Gilbert et al., 1991; Jiang et al., 2015). Horizontal microtubules emanate from the MTOC, which is at the level of the circumferential actin filaments (Jiang et al., 2015), and are perpendicular to the apical-basal axis of the cell (Figure 1). The majority of microtubules have their minus-ends at the level of the MTOC, but they are removed from the MTOC and are aligned vertically along the apical-basal axis of the cell; their plus-ends face the basal surface (Musch, 2004; Jiang et al., 2015) (Figure 1). Thus, the apical region of the cell is devoid of microtubules, except for those in the cilium, which extends from the apical surface; actin filaments occupy the entire apical region, including the apical microvilli.
FIGURE 1
In both polarized and nonpolarized cells, the microtubules serve as tracks for molecular motors that transport a variety of cargos (Toomre et al., 1999). Two families of motor proteins travel along microtubules. Kinesins are plus-end-directed motors while dyneins are minus-end-directed motors. The cargos transported by these two motors include, membrane-bound organelles, proteins, mRNA, and viruses (Cianfrocco et al., 2015). The kinesin superfamily of motors is quite diverse, with 15 identified families. Even with such diversity, kinesins require adaptor proteins that ensure specificity of cargo binding (Tempes et al., 2020). In contrast to the large kinesin family, dyneins are based on far fewer different motor subunits (heavy chains). However, these motor subunits associate with a large variety of other subunits, as well as adaptor proteins that are essential for cargo specificity and linkage to dynein in the cytoplasm of animal cells (Reck-Peterson et al., 2018). Moreover, the adaptor proteins allow the dynein motor to travel with processivity such that it does not detach from microtubules before reaching its destination (McKenney et al., 2014; Schlager et al., 2014). In the RPE, microtubule motors transport two important motile organelles necessary for their supportive function, including the pigment-containing melanosome and the POS-derived phagosome.
Transport of Melanosomes in the RPE
Melanosomes play an important role in the absorption of stray light in the eyes of invertebrates and vertebrates, with their movements providing a means to alter visual sensitivity and resolution. Examples are found among mollusks (Daw and Pearlman, 1974), arthropods (Boschek, 1971; Williams, 1982; 1983), and fish and amphibians (Back et al., 1965; Burnside and Basinger, 1983; Burnside, 2001; Burgoyne et al., 2015). In vertebrate eyes, cylindrically-shaped melanosomes enter the narrow apical processes of the RPE, which project among the POS, thus affecting light absorption by the POS. In addition to screening light, melanosomes may also contribute to the heavy phagocytic role of the RPE, as they contain proteases (Azarian et al., 2006), and have been observed to fused with phagosomes (Schraermeyer et al., 1999).
The localization of melanosomes to the actin-rich apical RPE is dependent on the actin-based motor protein, myosin-7a, which functionally associates with RPE melanosomes by linkage through RAB27A and the exophilin, MYRIP (El-Amraoui et al., 2002; Futter et al., 2004; Gibbs et al., 2004; Klomp et al., 2007; Lopes et al., 2007). This apical localization also requires cytoplasmic dynein, with lack of cytoplasmic dynein or myosin-7a resulting in comparable phenotypes (Liu et al., 1998; Jiang et al., 2020). It appears that dynein is responsible for delivering melanosomes from the cell body to the apical region of the RPE, and myosin-7a takes delivery and keeps them in the actin-rich, apical domain. However, in the cell body, melanosomes undergo bidirectional movements along microtubules (Jiang et al., 2020), suggesting the involvement of a kinesin as well as dynein (Figure 2A). Loss of kinesin-1 function (due to loss of KIF5B) affected melanosome motility, although, unlike loss of cytoplasmic dynein function, it did not have an obvious effect on overall melanosome localization (Jiang et al., 2020). In some instances, plus-end directed microtubule movement involves more than one kinesin (Shin et al., 2003; Miller et al., 2005; Twelvetrees et al., 2010; Nakajima et al., 2012). Perhaps loss of kinesin-1 function, together with the inhibition of a second kinesin, would completely inhibit plus-end directed movements, and thus have an overall effect on melanosome localization within the RPE.
FIGURE 2
Melanosome transport in the RPE can be compared to that in skin melanocytes, but there are significant distinctions. In melanocytes, there is a net migration of melanosomes from the cell body to the dendrites, in the periphery of the cell; from there they are delivered to the keratinocytes (Wasmeier et al., 2008; Hume and Seabra, 2011; Wu and Hammer, 2014; Moreiras et al., 2019). Melanosome movements along the microtubules are nevertheless bidirectional, with transport towards the nucleus driven by dynein (Byers et al., 2000). Their movement to the dendrites was proposed to be driven mainly by kinesin-1 (Ishida et al., 2012; Ishida et al., 2015). However, more recent evidence argues that kinesin-1 is not necessary for movement to the dendrites, and that it can be accomplished entirely by myosin-5a activity along cortical actin filaments (Evans et al., 2014; Robinson et al., 2017).
The dynein-driven motility of melanocyte melanosomes is an example of where dynein adaptor proteins have been reported to function as regulatory linkers between motor and cargo. The adaptors include melanoregulin (Ohbayashi et al., 2012) and Rab36 (Matsui et al., 2012). Interestingly, melanoregulin in the RPE appears to be involved in the maturation of POS-derived phagosomes rather than melanosome transport (Damek-Poprawa et al., 2009). Further studies are necessary to reveal the mechanisms by which melanosomes link to microtubule motors of the dynein and kinesin family.
Transport of Phagosomes in the RPE
The RPE plays an essential role in the renewal of the outer segments of photoreceptor cells (Young and Bok, 1969; Williams and Fisher, 1987). The outer segments contain thousands of lipid disk membranes, the site where phototransduction begins (Burns and Arshavsky, 2005). New disk membranes are continually synthesized and formed at the base of the POS (Young, 1967). The apical surface of the RPE faces the photoreceptor cells, with its apical microvilli interdigitating the POS. Following a circadian rhythm, the RPE phagocytizes the tips of the POS. The phagosome containing these lipid disk membranes is unique in its composition, and appears to undergo a series of interactions to be degraded properly (Bosch et al., 1993; Wavre-Shapton et al., 2014).
The processing of POS-derived phagosomes in the RPE is heavily dependent on their motor-dependent trafficking to ensure interactions with degradative organelles, including endosomes and lysosomes (Figure 2B). Studies by Herman and Steinberg showed that disruption of the microtubule cytoskeleton in tapetal RPE of the opossum impedes the movement of POS-derived phagosomes (Herman and Steinberg, 1982b; a). More recently, the association of POS-derived phagosomes with a light chain of the kinesin-1 motor (KLC1) was observed as the phagosomes transitioned from the apical region to the cell body of mouse RPE (Jiang et al., 2015). Lack of KLC1 in mouse RPE impaired the trafficking of the phagosomes towards the basal surface of the RPE as well as their degradation (Jiang et al., 2015). Interestingly, live-cell imaging of POS-derived phagosomes in primary mouse RPE cells has shown that these organelles exhibit bidirectional movements along the microtubules (Jiang et al., 2015; Hazim et al., 2016), suggesting the actions of opposing motors; although the exact role of the minus-end dynein motor in the transport of POS-derived phagosomes remains unclear. The bidirectional movement of phagosomes may be necessary to ensure sufficient interactions with early and late endosomes, which prime the phagosome for fusion with lysosomes. Bidirectional movements of phagosomes, particularly in combination with bidirectional movements of endolysosomes on the same or nearby microtubules, should increase the probability of interactions between phagosomes and endolysosomes. Presumably, the number of such interactions is related to the efficiency of phagosome maturation and degradation—and whether undigested lipid membranes accumulate (Keeling et al., 2019).
Although there is evidence that microtubule-based motor transport is essential for the proper trafficking of POS-derived phagosomes, and therefore their timely clearance, there is still a knowledge gap with respect to the transport mechanisms that underlie this process. This gap includes the mechanisms that regulate the bidirectional motility of the phagosome, as well as the identification of adaptor proteins that facilitate the recruitment of motor proteins to the phagosome membrane.
Motor Proteins in the Context of RPE and Retinal Pathology
The RPE is essential to retinal health. Most forms of macular degeneration, including age-related macular degeneration (AMD), a common affliction among the elderly (Wong et al., 2014), arise from primary lesions in the RPE. Several monogenic forms of retinal degeneration are also caused by mutations in genes that are expressed in the RPE; for example, mutations in MERTK (Gal et al., 2000), which cause retinitis pigmentosa, CHM (Cremers et al., 1990), which cause choroideremia, and MYO7A which cause Usher syndrome type 1B (Weil et al., 1995). Studies from animal models provide some insight into whether defects in the motility or localization of organelles transported by microtubule motors could contribute to RPE dysfunction and pathology.
Melanosomes in mouse models of choroideremia (Tolmachova et al., 2010) and Usher syndrome 1B (Liu et al., 1998) do not localize normally to the apical region, but these models also demonstrate other potentially more serious RPE defects, including retarded POS phagosome degradation (see below) (Gibbs et al., 2003; Gordiyenko et al., 2010; Lopes et al., 2011; Williams and Lopes, 2011; Wavre-Shapton et al., 2013). Whether this mislocalization contributes to retinal pathology is not known. Nevertheless, it seems that melanosome mislocalization could be a useful biomarker for diseases such as choroideremia and Usher syndrome 1B, since it may be detectable with advanced retinal imaging (Liu et al., 2019).
Given how important the trafficking of phagosomes is to their timely processing and clearance, it is perhaps no surprise that motility defects result in pathological conditions that affect the health of the RPE and therefore the retina. In mice lacking kinesin-1 light chain, phagosome degradation was delayed resulting in AMD-like symptoms in aged animals, including oxidative stress, complement system activation, and photoreceptor death (Jiang et al., 2015). Interestingly, a similar pathology was reported in mice with RPE-specific ablation of the orthologue of the CHM gene, which encodes Rab Escort Protein-1 (REP-1) (Wavre-Shapton et al., 2013). REP-1 functions in the prenylation of Rab proteins, which serve as regulators of membrane trafficking. REP-1 depletion in human fetal RPE has been shown to impair the association of POS-derived phagosomes with RAB7-positive late endosomes, thereby delaying their clearance by the RPE (Gordiyenko et al., 2010).
Defects in dynein-specific trafficking of phagosomes have also been shown to impair the clearance of these organelles by the RPE. In a mouse model of Stargardt 3 macular degeneration, phagosomes contain a mutant form of the elongation of very long-chain fatty acids 4 (ELOVL4) protein, and were found to exhibit increased association with dynein and reduced clearance (Esteve-Rudd et al., 2018). This study indicates that the content of the POS-derived phagosome is an important characteristic that affects the recruitment and association of motor proteins with organelles in the cell. With artificial phagosomes, generated by the phagocytosis of latex beads, the cholesterol content of the enclosing membrane has been shown to influence phagosome motility by the dynein motor (Rai et al., 2016). Targeted approaches to modify the POS content prior to RPE phagocytosis would provide a physiological system for testing how cholesterol, and other macromolecules, affect the trafficking and clearance of phagosomes. Elucidating these mechanisms would provide a better understanding of how motor dysfunction and impaired subcellular trafficking contribute to pathology in the RPE and the retina.
Statements
Author contributions
RH and DW researched and wrote the manuscript.
Funding
The study was supported by National Institutes of Health grants R01EY027442, R21EY031109, and P30EY00331 (DW).
Conflict of interest
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.
Publisher’s note
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References
1
AkhmanovaA.SteinmetzM. O. (2008). Tracking the Ends: a Dynamic Protein Network Controls the Fate of Microtubule Tips. Nat. Rev. Mol. Cel Biol9 (4), 309–322. 10.1038/nrm2369
2
AzarianS. M.McLeodI.LilloC.GibbsD.YatesJ. R.WilliamsD. S. (2006). Proteomic Analysis of Mature Melanosomes from the Retinal Pigmented Epithelium. J. Proteome Res.5 (3), 521–529. 10.1021/pr0502323
3
BacallaoR.AntonyC.DottiC.KarsentiE.StelzerE. H.SimonsK. (1989). The Subcellular Organization of Madin-Darby Canine Kidney Cells during the Formation of a Polarized Epithelium. J. Cel Biol109, 2817–2832. 10.1083/jcb.109.6.2817
4
BäckI.DonnerK. O.ReuterT. (1965). The Screening Effect of the Pigment Epithelium on the Retinal Rods in the Frog. Vis. Res5 (3), 101–111. 10.1016/0042-6989(65)90058-1
5
BoschE.HorwitzJ.BokD. (1993). Phagocytosis of Outer Segments by Retinal Pigment Epithelium: Phagosome-Lysosome Interaction. J. Histochem. Cytochem.41 (2), 253–263. 10.1177/41.2.8419462
6
BoschekG. B. (1971). On the fine Structure of the Peripheral Retina and Lamina Ganglionaris of the Fly, Musca domestica. Z. Zellforsch.118, 369–409. 10.1007/bf00331193
7
BréM. H.PepperkokR.HillA. M.LevilliersN.AnsorgeW.StelzerE. H.et al (1990). Regulation of Microtubule Dynamics and Nucleation during Polarization in MDCK II Cells. J. Cel Biol111, 3013–3021. 10.1083/jcb.111.6.3013
8
BurgoyneT.O'ConnorM. N.SeabraM. C.CutlerD. F.FutterC. E. (2015). Regulation of Melanosome Number, Shape and Movement in the Zebrafish Retinal Pigment Epithelium by OA1 and PMEL. J. Cel Sci.128 (7), 1400–1407. 10.1242/jcs.164400
9
BurnsM. E.ArshavskyV. Y. (2005). Beyond Counting Photons: Trials and Trends in Vertebrate Visual Transduction. Neuron48 (3), 387–401. 10.1016/j.neuron.2005.10.014
10
BurnsideB.BasingerS. (1983). Retinomotor Pigment Migration in the Teleost Retinal Pigment Epithelium. II. Cyclic-3',5'-Adenosine Monophosphate Induction of Dark-Adaptive Movement In Vitro. Invest. Ophthalmol. Vis. Sci.24, 16–23.
11
BurnsideB. (2001). Chapter 34 Light and Circadian Regulation of Retinomotor Movement. Prog. Brain Res.131, 477–485. 10.1016/s0079-6123(01)31038-5
12
ByersH. R.YaarM.EllerM. S.JalbertN. L.GilchrestB. A. (2000). Role of Cytoplasmic Dynein in Melanosome Transport in Human Melanocytes. J. Invest. Dermatol.114 (5), 990–997. 10.1046/j.1523-1747.2000.00957.x
13
CianfroccoM. A.DeSantisM. E.LeschzinerA. E.Reck-PetersonS. L. (2015). Mechanism and Regulation of Cytoplasmic Dynein. Annu. Rev. Cel Dev. Biol.31, 83–108. 10.1146/annurev-cellbio-100814-125438
14
CremersF. P. M.Van de PolD. J. R.Van KerkhoffL. P. M.WieringaB.RopersH.-H. (1990). Cloning of a Gene that Is Rearranged in Patients with Choroideraemia. Nature347, 674–677. 10.1038/347674a0
15
Damek-PoprawaM.DiemerT.LopesV. S.LilloC.HarperD. C.MarksM. S.et al (2009). Melanoregulin (MREG) Modulates Lysosome Function in Pigment Epithelial Cells. J. Biol. Chem.284 (16), 10877–10889. 10.1074/jbc.m808857200
16
DawN. W.PearlmanA. L. (1974). Pigment Migration and Adaptation in the Eye of the Squid, Loligo Pealei. J. Gen. Physiol.63, 22–36. 10.1085/jgp.63.1.22
17
El-AmraouiA.SchonnJ. S.Küssel-AndermannP.BlanchardS.DesnosC.HenryJ. P.et al (2002). MyRIP, a Novel Rab Effector, Enables Myosin VIIa Recruitment to Retinal Melanosomes. EMBO Rep.3 (5), 463–470. 10.1093/embo-reports/kvf090
18
EncaladaS. E.GoldsteinL. S. B. (2014). Biophysical Challenges to Axonal Transport: Motor-Cargo Deficiencies and Neurodegeneration. Annu. Rev. Biophys.43 (1), 141–169. 10.1146/annurev-biophys-051013-022746
19
Esteve-RuddJ.HazimR. A.DiemerT.PaniaguaA. E.VollandS.UmapathyA.et al (2018). Defective Phagosome Motility and Degradation in Cell Nonautonomous RPE Pathogenesis of a Dominant Macular Degeneration. Proc. Natl. Acad. Sci. USA115, 5468–5473. 10.1073/pnas.1709211115
20
EvansR. D.RobinsonC.BriggsD. A.ToothD. J.RamalhoJ. S.CanteroM.et al (2014). Myosin-Va and Dynamic Actin Oppose Microtubules to Drive Long-Range Organelle Transport. Curr. Biol.24 (15), 1743–1750. 10.1016/j.cub.2014.06.019
21
FentonA. R.JongensT. A.HolzbaurE. L. F. (2021). Mitochondrial Adaptor TRAK2 Activates and Functionally Links Opposing Kinesin and Dynein Motors. Nat. Commun.12 (1), 4578. 10.1038/s41467-021-24862-7
22
FutterC. E.RamalhoJ. S.JaissleG. B.SeeligerM. W.SeabraM. C. (2004). The Role of Rab27a in the Regulation of Melanosome Distribution within Retinal Pigment Epithelial Cells. MBoC15 (5), 2264–2275. 10.1091/mbc.e03-10-0772
23
GalA.LiY.ThompsonD. A.WeirJ.OrthU.JacobsonS. G.et al (2000). Mutations in MERTK, the Human Orthologue of the RCS Rat Retinal Dystrophy Gene, Cause Retinitis Pigmentosa. Nat. Genet.26 (3), 270–271. 10.1038/81555
24
GibbsD.AzarianS. M.LilloC.KitamotoJ.KlompA. E.SteelK. P.et al (2004). Role of Myosin VIIa and Rab27a in the Motility and Localization of RPE Melanosomes. J. Cel Sci117, 6473–6483. 10.1242/jcs.01580
25
GibbsD.KitamotoJ.WilliamsD. S. (2003). Abnormal Phagocytosis by Retinal Pigmented Epithelium that Lacks Myosin VIIa, the Usher Syndrome 1B Protein. Proc. Natl. Acad. Sci.100 (11), 6481–6486. 10.1073/pnas.1130432100
26
GilbertT.Le BivicA.QuaroniA.Rodriguez-BoulanE. (1991). Microtubular Organization and its Involvement in the Biogenetic Pathways of Plasma Membrane Proteins in Caco-2 Intestinal Epithelial Cells. J. Cel Biol113 (2), 275–288. 10.1083/jcb.113.2.275
27
GordiyenkoN. V.FarissR. N.ZhiC.MacDonaldI. M. (2010). Silencing of theCHMGene Alters Phagocytic and Secretory Pathways in the Retinal Pigment Epithelium. Invest. Ophthalmol. Vis. Sci.51 (2), 1143–1150. 10.1167/iovs.09-4117
28
HazimR.JiangM.Esteve-RuddJ.DiemerT.LopesV. S.WilliamsD. S. (2016). Live-Cell Imaging of Phagosome Motility in Primary Mouse RPE Cells. Adv. Exp. Med. Biol.854, 751–755. 10.1007/978-3-319-17121-0_100
29
HermanK. G.SteinbergR. H. (1982a). Phagosome Degradation in the Tapetal Retinal Pigment Epithelium of the Opossum. Invest. Ophthalmol. Vis. Sci.23 (3), 291–304.
30
HermanK. G.SteinbergR. H. (1982b). Phagosome Movement and the Diurnal Pattern of Phagocytosis in the Tapetal Retinal Pigment Epithelium of the Opossum. Invest. Ophthalmol. Vis. Sci.23 (3), 277–290.
31
HumeA. N.SeabraM. C. (2011). Melanosomes on the Move: a Model to Understand Organelle Dynamics. Biochem. Soc. Trans.39 (5), 1191–1196. 10.1042/bst0391191
32
IshidaM.OhbayashiN.FukudaM. (2015). Rab1A Regulates Anterograde Melanosome Transport by Recruiting Kinesin-1 to Melanosomes through Interaction with SKIP. Scientific Rep.5 (1), 8238. 10.1038/srep08238
33
IshidaM.OhbayashiN.MarutaY.EbataY.FukudaM. (2012). Functional Involvement of Rab1A in Microtubule-dependent Anterograde Melanosome Transport in Melanocytes. J. Cel Sci.125, 5177. 10.1242/jcs.109314
34
JiangM.PaniaguaA. E.VollandS.WangH.BalajiA.LiD. G.et al (2020). Microtubule Motor Transport in the Delivery of Melanosomes to the Actin-Rich Apical Domain of the Retinal Pigment Epithelium. J. Cel Sci133, 1–10. 10.1242/jcs.242214
35
JiangM.Esteve-RuddJ.LopesV. S.DiemerT.LilloC.RumpA.et al (2015). Microtubule Motors Transport Phagosomes in the RPE, and Lack of KLC1 Leads to AMD-like Pathogenesis. J. Cel Biol210 (4), 595–611. 10.1083/jcb.201410112
36
KeelingE.ChateletD. S.JohnstonD. A.PageA.TumbarelloD. A.LoteryA. J.et al (2019). Oxidative Stress and Dysfunctional Intracellular Traffic Linked to an Unhealthy Diet Results in Impaired Cargo Transport in the Retinal Pigment Epithelium (RPE). Mol. Nutr. Food Res.63, e1800951. 10.1002/mnfr.201800951
37
KlompA. E.TeofiloK.LegackiE.WilliamsD. S. (2007). Analysis of the Linkage of MYRIP and MYO7A to Melanosomes by RAB27A in Retinal Pigment Epithelial Cells. Cell Motil. Cytoskeleton64 (6), 474–487. 10.1002/cm.20198
38
LakkarajuA.UmapathyA.TanL. X.DanieleL.PhilpN. J.Boesze-BattagliaK.et al (2020). The Cell Biology of the Retinal Pigment Epithelium. Prog. Retin. Eye Res.78, 100846. 10.1016/j.preteyeres.2020.100846
39
LiuX.OndekB.WilliamsD. S. (1998). Mutant Myosin VIIa Causes Defective Melanosome Distribution in the RPE of Shaker-1 Mice. Nat. Genet.19, 117–118. 10.1038/470
40
LiuZ.KurokawaK.HammerD. X.MillerD. T. (2019). In Vivo measurement of Organelle Motility in Human Retinal Pigment Epithelial Cells. Biomed. Opt. Express10 (8), 4142. 10.1364/boe.10.004142
41
LopesV. S.GibbsD.LibbyR. T.AlemanT. S.WelchD. L.LilloC.et al (2011). The Usher 1B Protein, MYO7A, Is Required for normal Localization and Function of the Visual Retinoid Cycle Enzyme, RPE65. Hum. Mol. Genet.20, 2560. 10.1093/hmg/ddr155
42
LopesV. S.RamalhoJ. S.OwenD. M.KarlM. O.StraussO.FutterC. E.et al (2007). The Ternary Rab27a-Myrip-Myosin VIIa Complex Regulates Melanosome Motility in the Retinal Pigment Epithelium. Traffic8 (5), 486–499. 10.1111/j.1600-0854.2007.00548.x
43
MatsuiT.OhbayashiN.FukudaM. (2012). The Rab Interacting Lysosomal Protein (RILP) Homology Domain Functions as a Novel Effector Domain for Small GTPase Rab36. J. Biol. Chem.287 (34), 28619–28631. 10.1074/jbc.M112.370544
44
McKenneyR. J.HuynhW.TanenbaumM. E.BhabhaG.ValeR. D. (2014). Activation of Cytoplasmic Dynein Motility by Dynactin-Cargo Adapter Complexes. Science345, 337–341. 10.1126/science.1254198
45
MillerK. E.DeProtoJ.KaufmannN.PatelB. N.DuckworthA.Van VactorD. (2005). Direct Observation Demonstrates that Liprin-α Is Required for Trafficking of Synaptic Vesicles. Curr. Biol.15, 684–689. 10.1016/j.cub.2005.02.061
46
MitchisonT.KirschnerM. (1984). Dynamic Instability of Microtubule Growth. Nature312, 237–242. 10.1038/312237a0
47
MoreirasH.Lopes‐da‐SilvaM.SeabraM. C.BarralD. C. (2019). Melanin Processing by Keratinocytes: A Non‐microbial Type of Host‐pathogen Interaction?Traffic20 (4), 301–304. 10.1111/tra.12638
48
MüschA. (2004). Microtubule Organization and Function in Epithelial Cells. Traffic5, 1–9. 10.1111/j.1600-0854.2003.00149.x
49
NakajimaK.YinX.TakeiY.SeogD.-H.HommaN.HirokawaN. (2012). Molecular Motor KIF5A Is Essential for GABAA Receptor Transport, and KIF5A Deletion Causes Epilepsy. Neuron76, 945–961. 10.1016/j.neuron.2012.10.012
50
OhbayashiN.MarutaY.IshidaM.FukudaM. (2012). Melanoregulin Regulates Retrograde Melanosome Transport through Interaction with the RILP·p150Glued Complex in Melanocytes. J. Cel Sci.125, 1508. 10.1242/jcs.094185
51
RaiA.PathakD.ThakurS.SinghS.DubeyA. K.MallikR. (2016). Dynein Clusters into Lipid Microdomains on Phagosomes to Drive Rapid Transport toward Lysosomes. Cell164 (4), 722–734. 10.1016/j.cell.2015.12.054
52
Reck-PetersonS. L.RedwineW. B.ValeR. D.CarterA. P. (2018). The Cytoplasmic Dynein Transport Machinery and its many Cargoes. Nat. Rev. Mol. Cel Biol19 (6), 382–398. 10.1038/s41580-018-0004-3
53
RobinsonC. L.EvansR. D.BriggsD. A.RamalhoJ. S.HumeA. N. (2017). Deficiency in Kinesin-1 Recruitment to Melanosomes Precludes it from Facilitating Their Centrifugal Transport. J. Cel Sci.130, 2056. 10.1242/jcs.186064
54
SchlagerM. A.HoangH. T.UrnaviciusL.BullockS. L.CarterA. P. (2014). In Vitro reconstitution of a Highly Processive Recombinant Human Dynein Complex. Embo J.33 (17), 1855–1868. 10.15252/embj.201488792
55
SchraermeyerU.PetersS.ThumannG.KociokN.HeimannK. (1999). Melanin Granules of Retinal Pigment Epithelium Are Connected with the Lysosomal Degradation Pathway. Exp. Eye Res.68 (2), 237–245. 10.1006/exer.1998.0596
56
ShinH.WyszynskiM.HuhK.-H.ValtschanoffJ. G.LeeJ.-R.KoJ.et al (2003). Association of the Kinesin Motor KIF1A with the Multimodular Protein Liprin-α. J. Biol. Chem.278, 11393–11401. 10.1074/jbc.m211874200
57
StraussO. (2005). The Retinal Pigment Epithelium in Visual Function. Physiol. Rev.85 (3), 845–881. 10.1152/physrev.00021.2004
58
TempesA.WeslawskiJ.BrzozowskaA.JaworskiJ. (2020). Role of Dynein-Dynactin Complex, Kinesins, Motor Adaptors, and Their Phosphorylation in Dendritogenesis. J. Neurochem.155 (1), 10–28. 10.1111/jnc.15010
59
TolmachovaT.Wavre-ShaptonS. T.BarnardA. R.MacLarenR. E.FutterC. E.SeabraM. C. (2010). Retinal Pigment Epithelium Defects Accelerate Photoreceptor Degeneration in Cell Type-specific Knockout Mouse Models of Choroideremia. Invest. Ophthalmol. Vis. Sci.51 (10), 4913. 10.1167/iovs.09-4892
60
ToomreD.KellerP.WhiteJ.OlivoJ. C.SimonsK. (1999). Dual-color Visualization of Trans-golgi Network to Plasma Membrane Traffic along Microtubules in Living Cells. J. Cel Sci112, 21–33. 10.1242/jcs.112.1.21
61
Ts'oM. O. M.FriedmanE. (1967). The Retinal Pigment Epithelium. Arch. Ophthalmol.78, 641–649. 10.1001/archopht.1967.00980030643016
62
TwelvetreesA. E.YuenE. Y.Arancibia-CarcamoI. L.MacAskillA. F.RostaingP.LumbM. J.et al (2010). Delivery of GABAARs to Synapses Is Mediated by HAP1-KIF5 and Disrupted by Mutant Huntingtin. Neuron65, 53–65. 10.1016/j.neuron.2009.12.007
63
VollandS.Esteve-RuddJ.HooJ.YeeC.WilliamsD. S. (2015). A Comparison of Some Organizational Characteristics of the Mouse central Retina and the Human Macula. PLoS One10 (4), e0125631. 10.1371/journal.pone.0125631
64
VorobjevI. A.NadezhdinaE. S. (1987). The Centrosome and its Role in the Organization of Microtubules. Int. Rev. Cytol.106, 227–293. 10.1016/s0074-7696(08)61714-3
65
WasmeierC.HumeA. N.BolascoG.SeabraM. C. (2008). Melanosomes at a Glance. J. Cel Sci121, 3995–3999. 10.1242/jcs.040667
66
Wavre-ShaptonS. T.MeschedeI. P.SeabraM. C.FutterC. E. (2014). Phagosome Maturation during Endosome Interaction Revealed by Partial Rhodopsin Processing in Retinal Pigment Epithelium. J. Cel Sci127 (Pt 17), 3852–3861. 10.1242/jcs.154757
67
Wavre-ShaptonS. T.TolmachovaT.da SilvaM. L.FutterC. E.SeabraM. C. (2013). Conditional Ablation of the Choroideremia Gene Causes Age-Related Changes in Mouse Retinal Pigment Epithelium. PloS one8 (2), e57769. 10.1371/journal.pone.0057769
68
WeilD.BlanchardS.KaplanJ.GuilfordP.GibsonF.WalshJ.et al (1995). Defective Myosin VIIA Gene Responsible for Usher Syndrome Type 1B. Nature374, 60–61. 10.1038/374060a0
69
WilliamsD. S.FisherS. K. (1987). Prevention of Rod Disk Shedding by Detachment from the Retinal Pigment Epithelium. Invest. Ophthalmol. Vis. Sci.28, 184–187.
70
WilliamsD. S. (1982). Ommatidial Structure in Relation to Turnover of Photoreceptor Membrane in the Locust. Cell Tissue Res225 (3), 595–617. 10.1007/BF00214807
71
WilliamsD. S. (1983). Changes of Photoreceptor Performance Associated with the Daily Turnover of Photoreceptor Membrane in Locusts. J. Comp. Physiol.150, 509–519. 10.1007/bf00609577
72
WilliamsD. S.LopesV. S. (2011). The many Different Cellular Functions of MYO7A in the Retina. Biochem. Soc. Trans.39 (5), 1207–1210. 10.1042/BST0391207
73
WongW. L.SuX.LiX.CheungC. M. G.KleinR.ChengC.-Y.et al (2014). Global Prevalence of Age-Related Macular Degeneration and Disease burden Projection for 2020 and 2040: a Systematic Review and Meta-Analysis. Lancet Glob. Health2 (2), e106–e116. 10.1016/S2214-109X(13)70145-1
74
WuX.HammerJ. A. (2014). Melanosome Transfer: it Is Best to Give and Receive. Curr. Opin Cel Biol.29, 1–7. 10.1016/j.ceb.2014.02.003
75
YoungR. W.BokD. (1969). Participation of the Retinal Pigment Epithelium in the Rod Outer Segment Renewal Process.J. Cel Biol42, 392–403. 10.1083/jcb.42.2.392
76
YoungR. W. (1967). The Renewal of Photoreceptor Cell Outer Segments. J. Cel Biol.33 (1), 61–72. 10.1083/jcb.33.1.61
77
ZhaoC.YasumuraD.LiX.MatthesM.LloydM.NielsenG.et al (2011). mTOR-Mediated Dedifferentiation of the Retinal Pigment Epithelium Initiates Photoreceptor Degeneration in Mice. J. Clin. Invest.121 (1), 369–383. 10.1172/JCI44303
Summary
Keywords
RPE—retinal pigment epithelium, organelle transport, kinesin, dynein, retinal degeneration
Citation
Hazim RA and Williams DS (2022) Microtubule Motor Transport of Organelles in a Specialized Epithelium: The RPE. Front. Cell Dev. Biol. 10:852468. doi: 10.3389/fcell.2022.852468
Received
11 January 2022
Accepted
01 February 2022
Published
04 March 2022
Volume
10 - 2022
Edited by
Xin Xiang, Uniformed Services University of the Health Sciences, United States
Reviewed by
Thomas Burgoyne, University College London, United Kingdom
Clare Futter, University College London, United Kingdom
Updates
Copyright
© 2022 Hazim and Williams.
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) and the copyright owner(s) 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: Roni A. Hazim, rhazim@ucla.edu; David S. Williams, dswilliams@ucla.edu
This article was submitted to Membrane Traffic, a section of the journal Frontiers in Cell and Developmental Biology
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