Reciprocal Relationship Between Calcium Signaling and Circadian Clocks: Implications for Calcium Homeostasis, Clock Function, and Therapeutics

GRAPHICAL ABSTRACT

Graphical Abstract. Reciprocal relationship between Ca²⁺ signaling and the circadian clock. In Drosophila and mice, circadian clocks impose a daily rhythmicity to Ca²⁺ signaling; and, conversely, Ca²⁺ rhythms and signaling contribute to transmitting daily external signals to the clock TTFL. This bidirectional regulation is critical to the daily rhythmicity of many physiological and behavioral processes.

Introduction

All multicellular animals contain a biological clock that allows them to anticipate the daily changes in the environment, such as the arrival of dawn or dusk. These are endogenous mechanisms that are cell-autonomous and are invariably controlled by highly conserved intracellular transcription-translation feedback loops (TTFL) (Hardin, 2011; Takahashi, 2017). At their core, these TTFLs include the transcription factors, CLOCK and CYCLE (usually called BMAL1 in mammals), which activate the transcription of the period (per) and either the timeless (tim) or the cryptochrome (cry) genes in Drosophila and mammals, respectively. In the cytoplasm, the corresponding PER and either TIM (Drosophila) or CRY (mammals) proteins dimerize, re-enter the nucleus, and inhibit the activity of CLOCK-CYCLE, thereby preventing their own expression. The exact functioning of this core TTFL is, in addition, modified by a growing number of intracellular factors, which include additional secondary TTFLs, kinases and phosphatases that regulate the stability of PER and TIM (CRY) proteins, as well as chromatin and chromatin-modifying complexes, all of which contribute to producing a molecular rhythm with near-24 h periodicity. Circadian clocks are classified according to where they reside: central oscillators are located in the brain whereas peripheral oscillators can be housed in a wide variety of tissues, where they impose a daily rhythmicity to the physiology of each organ (Mohawk et al., 2012). Yet, the different cells that make up the central oscillators must coordinate their activity and must also be entrainable by the daily environmental signals that synchronize the organism’s pattern of activity to the appropriate time of day (usually light, but for ectothermal animals can also be temperature). In addition, peripheral clocks are coordinated with the central clock to produce a unitary biological time for the organism. And, finally, the activity of clocks can in turn be modified by the organism’s physiology and/or behavior (e.g., through feeding, Damiola et al., 2000). At the systems level, the entrainment of central and peripheral clocks, the coordination between clocks as well as between clocks and their host, occurs via neuronal, endocrine, and paracrine signals (Schibler et al., 2015; King and Sehgal, 2020). These signals are transduced by various signaling pathways that ultimately alter the temporal pattern of gene expression. Here, we review the role of Ca²⁺ in clock function by considering intracellular and extracellular signals that regulate Ca²⁺ levels in circadian clocks (see section “Ca²⁺ Rhythms in Biological Clocks Are Regulated by Intracellular and Extracellular Signals”). In addition, we discuss the mechanism by which Ca²⁺ signaling affects clock function (see section “Effects of Ca²⁺ Signaling on the Expression of Clock Genes and Rhythmic Behavior”), and, in turn, how clock function affects Ca²⁺ signaling (see section “Circadian Regulation of Ca²⁺ Associated Proteins”). Finally, as a result of our growing appreciation of the importance of clocks in health and disease, we discuss how our knowledge of the reciprocal relationship between clocks and Ca²⁺ signaling impacts the effectiveness of drugs and is relevant to the development of improved therapeutics (see section “Ca²⁺ Signaling and Clocks: Implications for Diseases and Chronomedicine”).

Ca²⁺ Rhythms in Biological Clocks Are Regulated by Intracellular and Extracellular Signals

In animals, intracellular Ca²⁺ levels ([Ca²⁺]_i) are essential for the proper functioning of many cellular and physiological processes, including circadian rhythms. For example, in the case of pacemakers housed within neuronal tissues, fluctuations in [Ca²⁺]_i have been associated with the circadian control of neuropeptide release, the expression of clock genes, synaptic plasticity, and the periodicity of rhythmic behaviors (Lundkvist et al., 2005; Harrisingh et al., 2007; Depetris-Chauvin et al., 2011). For this reason, an important area of research in chronobiology is devoted to identifying changes in [Ca²⁺]_i that occur in circadian pacemaker neurons and understanding their origin. Interestingly, daily Ca²⁺ variations occur in circadian oscillators of rodents (Colwell, 2000; Ikeda et al., 2003; Enoki et al., 2012, 2017; Brancaccio et al., 2013; Noguchi et al., 2017), flies (Liang et al., 2016; Guo et al., 2017), and mollusks (Colwell et al., 1994).

Neuropeptide-Mediated Ca²⁺ Rhythms

In mice, Ca²⁺ rhythms have been described in neurons and astrocytes of the central mammalian clock, which is located in the suprachiasmatic nucleus (SCN) (Ikeda et al., 2003; Brancaccio et al., 2017). Remarkably, they are not uniform over the entire nucleus. Indeed, the phase of Ca²⁺ oscillations in dorsal regions are advanced relative to those in the ventral zone, and this spatial organization is highly dependent on neuronal network properties within the SCN (Enoki et al., 2012; Brancaccio et al., 2013). In addition, this difference in Ca²⁺ phase is abolished when the intercellular synchronization within the SCN is weak (Enoki et al., 2017), suggesting that diffusible factors such as the neuropeptides, arginine vasopressin (AVP) or vasoactive intestinal peptide (VIP), which are enriched in dorsal and ventral regions of SCN, respectively (see Figure 4 from Enoki et al., 2017), are relevant for maintaining the phase difference between Ca²⁺ oscillations in the dorsal vs. ventral SCN. Similarly, in Drosophila, where daily locomotor activity shows a bi-modal pattern, the central clock neurons that control the morning and the evening peaks of activity express different Ca²⁺ phases (Liang et al., 2016). In particular, neurons that regulate the morning activity (the so-called M-cells) exhibit an advanced Ca²⁺ phase relative to circadian pacemaker neurons that control the evening activity (the so-called E-cells) (see Figure 2 in Kozlov and Nagoshi, 2019). Remarkably, inhibiting signaling mediated by pigment dispersing factor (PDF), a neuropeptide analogous to mammalian VIP, causes the phases of Ca²⁺ oscillations in M and E cells to be synchronous (Liang et al., 2016) and the pattern of behavior to be unimodal or arrhythmic (Hyun et al., 2005). In addition, in Drosophila, [Ca²⁺]_i varies during the course of the day in the prothoracic gland (PG), a peripheral clock that regulates the circadian rhythm of adult eclosion (Morioka et al., 2012; Palacios-Munoz and Ewer, 2018). A study carried out in organotypic PG cultures shows that the phase of the Ca²⁺ oscillations is set by inputs from the brain (Morioka et al., 2012), which are probably mediated by prothoracicotropic hormone, a neuropeptide that transmits time information from the central clock to the PG (Selcho et al., 2017). Of note, Ca²⁺ plays a critical role in the synthesis and release of the molting hormone, ecdysone, from the PG (Huang et al., 2008; Smith et al., 2012; Yamanaka et al., 2015), suggesting that fluctuations in [Ca²⁺]_i due to clock activity could produce a daily rhythm in hemolymph ecdysone titers and, consequently, be relevant to the circadian control of adult emergence. Nevertheless, although such oscillations occur in some insects (Ampleford and Steel, 1985), they have not been detected in Drosophila.

Clock Genes and Ca²⁺ Oscillations

Although neuropeptides can set the phase of Ca²⁺ oscillations in biological clocks, these extracellular signals are not the only relevant ones for regulating Ca²⁺ rhythms. In mice, an early study using FURA-2, a synthetic fluorescent Ca²⁺-sensitive dye, showed that Ca²⁺ oscillations are completely abolished by tetrodotoxin (TTX) treatments, suggesting that neuronal firing of SCN neurons is essential for maintaining these rhythms (Colwell, 2000). However, FURA-2 does not allow for the long-term measurement of Ca²⁺ oscillations because it is eventually cleared from the cytoplasm. In contrast to these results, studies that have expressed genetically encoded Ca²⁺ sensors such as GCaMP or Cameleon in the SCN have shown that Ca²⁺ rhythms are only partially reduced in the absence of neuronal firing, suggesting that intracellular signaling and possibly also non-action potential dependent signaling (e.g., Hablitz et al., 2020) also plays a role in regulating the oscillations of [Ca²⁺]_i (Enoki et al., 2012; Noguchi et al., 2017). Intracellular pathways could be associated with TTFLs of clock genes. Indeed, in mammals, overexpression of a dominant-negative allele of BMAL1, a transcription factor and core element of the clock, inhibits Ca²⁺ rhythms in the SCN (Ikeda and Ikeda, 2014). Similarly, in Drosophila a null allele of the period gene, which is also a core component of the clock, reduces the rhythm and coherence of Ca²⁺ oscillations in central clock neurons (Liang et al., 2016), and similar results have been described for the peripheral clock housed in the prothoracic gland (Palacios-Munoz and Ewer, 2018).

Photic Inputs Set the Phase of Ca²⁺ Oscillations

A third regulator of intracellular Ca²⁺ rhythms is photic inputs. Light is the most potent signal for phase shifting and for entraining circadian rhythms of behavior. In the mammalian SCN, light causes a time-dependent shift in the phase of the spontaneous Ca²⁺ oscillations exhibited by neurons that produce VIP, which are critical for propagating photic inputs through the SCN as well as for resetting the daily rhythms (Jones et al., 2018). Consistent with this, the behavioral rhythms of mice lacking calbindin (a cytosolic Ca²⁺-buffering protein) display increased phase delays when they receive a light stimulus in the early part of the night (Stadler et al., 2010). Interestingly, in rodents, photic inputs also regulate Ca²⁺ rhythms using intracellular stores (Ding et al., 1998; Ikeda et al., 2003; Aguilar-Roblero et al., 2007). Indeed, blockers of the ryanodine receptor impair Ca²⁺ oscillations in organotypic cultures of rat SCN (Ding et al., 1998), suggesting that the release of Ca²⁺ from the endoplasmic reticulum is critical for the regulation of the rhythm of [Ca²⁺]_i in the mammalian central clock. On other hand, in Drosophila, photic inputs set the phase of Ca²⁺ oscillations in central clock neurons through two pathways: they either act through the visual system via PDF, or they act directly on the circadian pacemaker through the internal photoreceptor, CRYPTOCROME (CRY), to set the phase of a group of E-cell neurons (Liang et al., 2017). By contrast, in the PG, CRY-dependent photoreception inhibits Ca²⁺ activity and this effect is abolished when the brain-PG complex is treated with TTX, suggesting that in this peripheral oscillator the actions of light are mediated by neuronal pathways from the brain (Morioka et al., 2012). In insects, light can also penetrate the translucid exoskeleton and entrain peripheral clocks; however, whether these photic inputs can directly affect the Ca²⁺ rhythms of pacemaker neurons is currently unknown.

Overall, this evidence suggests that Ca²⁺ rhythms in circadian clocks are regulated by both intracellular and extracellular signals. In addition, extracellular signals from neuropeptides and photic inputs can set the phase of these rhythms and coordinate the relative timing of the Ca²⁺ oscillations (Figure 1A), whereas TTFLs, and probably also intracellular Ca²⁺ stores, can contribute to generate Ca²⁺ oscillations in circadian clocks (Figure 2A). This model is based on the proposal that the central clock is comprised of interconnected autonomous circadian oscillators whose emerging network properties reinforce their circadian rhythmicity, synchronizing their oscillations, and adjusting them to the day-night cycles (Welsh et al., 2010).

FIGURE 1

Figure 1. Ca²⁺ signaling modulates the core components of the circadian clock. (A) In Drosophila and mammals, intracellular cytosolic Ca²⁺ rhythms are regulated by external signals such as light stimuli and neuropeptides. (B) In the SCN, external signals may affect the TTFL via the G_q-Ca²⁺ pathway. In turn, Ca²⁺ signaling via CREB and the regulation of the phosphorylation state (C) and proteasomal degradation (D) of clock proteins, orchestrate the effect of Ca²⁺ on the circadian clock in Drosophila and mammals. BMAL1, Brain and Muscle ARNT-Like 1, ortholog of Drosophila Cycle gene; CaMK, Ca²⁺/calmodulin-dependent protein kinase. CLOCK, Circadian Locomotor Output Cycles Kaput; CREB, cAMP response element-binding protein; CRE elements, cAMP response elements; CRY, cryptochrome; E-box, circadian enhancer box; ER, endoplasmic reticulum; PER, PERIOD protein; PKC, protein kinase C; ROR-α, retinoid-related orphan receptor alpha; TIM, TIMELESS protein.

FIGURE 2

Figure 2. Circadian clocks impose a daily rhythm on intracellular Ca²⁺ signaling. (A) Photic inputs via CRY or other signaling molecules such as PLC cause a phase-shift in the expression of molecular clock components in the mammalian and Drosophila central clocks. In turn, TTFL regulate cytosolic Ca²⁺ rhythms. In SCN neurons, circadian oscillations of Ca²⁺ levels are also dependent on the mobilization of Ca²⁺ from the endoplasmic reticulum. (B) Circadian clocks impose a daily rhythm of expression to a large number of components of the Ca²⁺ signaling pathway by acting at transcriptional or post-transcriptional levels (including by regulating alternative splicing in Drosophila and microRNA in mice). In addition, in mice, the Ca²⁺/calcineurin/NFAT pathway exhibits a rhythmic activity in peripheral clocks, such as the one present in skeletal muscle or heart, which is probably mediated by inputs from the central clock. IP₃R, inositol 1,4,5-triphosphate Receptor; NFAT, nuclear factor of activated T-cells; RORE, ROR response elements. RCAN1, regulator of calcineurin 1. RyR, ryanodine receptor. SERCA, sarcoplasmic/endoplasmic reticulum Ca²⁺ ATPase. See Figure 1 for other abbreviations.

Effects of Ca²⁺ Signaling on the Expression of Clock Genes and Rhythmic Behavior

In multicellular organisms, a variety of molecules are critical for sustaining circadian behavior. In Drosophila and mammals, transcription factors, microRNAs, and protein kinases, control the proper functioning of biological clocks (Patke et al., 2020). Interestingly, Ca²⁺ signaling is also involved in driving rhythmic behaviors and rhythms of gene expression. In Drosophila, genetic manipulations that decrease Ca²⁺ levels or reduce the expression of proteins such as Ca²⁺/calmodulin-dependent protein kinase II (CaMKII) in circadian pacemaker neurons, lengthen the periodicity of the circadian rhythms of locomotor activity and of adult eclosion (Harrisingh et al., 2007; Palacios-Munoz and Ewer, 2018). Similarly, a mouse bearing a mutation in the CaMKII gene that abolishes all kinase activity exhibits a longer free-running period of locomotor activity and a desynchronization between the molecular rhythms of the left and right nuclei of the SCN (Kon et al., 2014). In terms of gene expression, buffering intracellular Ca²⁺ abolishes Per1 oscillations in cultured SCN slices, and voltage-gated Ca²⁺ channel antagonists dampen the rhythm of Per2 and Bmal1 in an SCN cell line (Lundkvist et al., 2005; Nahm et al., 2005). Likewise, in the peripheral clock of the rat liver, lowering extracellular [Ca²⁺] abolishes Per1 rhythmicity (Lundkvist et al., 2005). Remarkably, blocking Ca²⁺ flux mediated by the 1,4,5-trisphosphate receptor (IP₃R) and the sarco/endoplasmic reticulum Ca²⁺ ATPase (SERCA) in rat liver explants lengthens the period of Per1-luc oscillations (Baez-Ruiz and Diaz-Munoz, 2011), which provides additional evidence that intracellular Ca²⁺ stores play a key role in the generation of circadian rhythms.

The growing evidence of the role of Ca²⁺ in the control of the clock genes expression raises the question of how Ca²⁺ signaling would influence the TTFL. To date, three mechanism has been proposed: (a) regulation via Ca²⁺/cAMP-responsive elements (CREs); and by modifying the phosphorylation state of clock proteins that affect the functioning of TTFLs at (b) the transcriptional or (c) the post-translational level.

Ca²⁺/cAMP-Responsive Elements

cAMP-responsive element is a sequence that binds CRE-binding protein (CREB) and is present within the promoter region of several mammalian clock genes (Zhang et al., 2005). In flies and mice, CREB induces changes in clock gene expression in response to light and contributes to the synchronization of activity among pacemaker cells (Ginty et al., 1993; Welsh et al., 2010; Tanenhaus et al., 2012). Several findings suggest that CREB is critical for integrating the signaling mediated by second messengers, such as Ca²⁺, into the rhythm of expression of clock genes. For instance, in the hamster SCN, the phase-shifts in Per1 and Per2 induced by light are mediated by CaMKII (Yokota et al., 2001), which can stimulate CRE-promotor activity through the phosphorylation of CREB (Figure 1B) (Nomura et al., 2003). In addition to actions mediated through CaMK signaling, manipulations of electrical activity in neurons reveals a close relationship between Ca²⁺-induced changes in CREB expression and alterations in TTFL. In Drosophila, for example, the hyperexcitation of a cluster of clock neurons triggers a morning-like transcriptome profile whereas their hyperpolarization induces an evening-like transcription state (Mizrak et al., 2012). Many of the genes differentially expressed in response to electrical activity code for K⁺ channels and proteins that are part of the PKC, PI₃K, and MAPK signaling pathways, and are enriched in CRE elements in their promotor region. In addition, manipulating the state of excitability of clock neurons regulates CREB expression, respectively, increasing or decreasing its levels in response to depolarization or hyperpolarization at night (Mizrak et al., 2012). These findings suggest that, in Drosophila, the electrical state of clock neurons imposes a daily rhythm to the transcriptional profile via CREB. On other hand, assays using a CRE-luciferase reporter system have shown that CRE-mediated transcription exhibits a circadian rhythmicity in neurons and glia in multiple areas of the Drosophila brain (Tanenhaus et al., 2012); in the mouse SCN, this oscillation is highly dependent on the Gq-Ca²⁺ axis (Figure 1B) (Brancaccio et al., 2013). In particular, the Ca²⁺ peak occurs earlier than the CRE-luc peak, which in turn, precedes the peaks in Per1-luc and Per2-luc activity (see in Figure 4 from Enoki et al., 2017). Remarkably, the activation of the G_q-dependent pathways using DREADDs (designer receptor exclusively activated by designer drug) reorganizes this hierarchical organization altering Ca²⁺ rhythms in clocks cells and lengthening the period of CRE-luc and Per-luc cycling in the SCN. These effects are not mediated through G_s or G_i, indicating that CRE-mediated transcription is exclusively activated through the Gq-Ca²⁺ axis.

Ca²⁺ Signaling and Transcriptional Changes Mediated by Phosphorylation of Clock Proteins

The phosphorylation state of clock proteins plays a pivotal role in the functioning of circadian clocks. Indeed, mutations in a variety of protein kinase and phosphatases alter the rhythm of circadian behaviors in flies, hamsters, mice, and humans (Reischl and Kramer, 2011). At the molecular level, kinase activity can regulate the transcription levels of canonical clocks genes, their accumulation in the nucleus, their ability to bind other proteins, and their stability (Gallego and Virshup, 2007). Interestingly, Ca²⁺ signaling has been implicated in the control of the phosphorylation state of clock proteins (Figure 1C). For instance, protein kinase C (PKC) and phospholipase C are critical to light-induced clock resetting in mice (Jakubcakova et al., 2007) and Drosophila (Saint-Charles et al., 2016; Ogueta et al., 2018, 2020), respectively. In the mouse SCN, the adaptation to photic stimuli is highly dependent on the phosphorylation state of chromatin modifiers mediated by PKC. In particular, PKCα phosphorylates a lysine-specific demethylase 1 (LSD1) that controls the phase resetting of pacemaker cells and the circadian control of locomotor activity in mice (Nam et al., 2014). At the molecular level, phosphorylated LSD1 binds the BMAL1/CLOCK complex, which controls the pattern of expression of clock genes that contain an E-box sequence (a circadian transcriptional enhancer) in their promotor region (Nam et al., 2014). In addition, in a variety of mammalian cell types, PKCα can act autonomously on core clock proteins, for instance by phosphorylating BMAL1, and this activity is enhanced by RACK1 (receptor for activated C kinase-1), a signaling protein that recruits PKC to its substrates (Robles et al., 2010). The PKCα/RACK-1 complex is recruited to BMAL1 in a circadian manner in central and peripheral mammalian pacemakers. In a fibroblast cell line, the PKCα/RACK1 complex controls the circadian period by acting as a negative regulator of BMAL1-CLOCK transcriptional activity, which supports the idea that PKC plays a key role in regulating mammalian circadian clocks (Robles et al., 2010). CaMKII is another protein associated with Ca²⁺ signaling that directly phosphorylates core clock proteins in the mouse SCN. Indeed, in pacemaker cells of this brain area, this protein kinase phosphorylates CLOCK in a circadian manner by promoting BMAL1-CLOCK heteromerization and enhancing E-box-dependent gene expression including that of Per1-3 and Cry1 (Kon et al., 2014). Remarkably, in the mammalian SCN, the pattern of expression of these genes is also altered by calmodulin inhibitors and Ca²⁺ chelators (Kon et al., 2014), indicating that the Ca²⁺/calmodulin/CaMKII-mediated phosphorylation of CLOCK is an important regulator of cell-autonomous clockwork periodicity.

Ca²⁺ Signaling and Posttranslational Modifications Mediated by the Phosphorylation of Clock Proteins

In the circadian clocks of flies and mammals, the actions mediated through Ca²⁺ modulation of kinase/phosphatase activity are not restricted to the nucleus of pacemaker cells (Figure 1D). For instance, transfection of PKC in mammalian cell lines increases the stability of PER2 and promotes its cytoplasmic localization (Jakubcakova et al., 2007). These effects are independent of the CREB pathway and may involve CK1ε (casein kinase 1 epsilon), which is known to regulate the proteasomal degradation of PER2 and its shuttling between the cytoplasm and the nucleus (Akashi et al., 2002; Eide et al., 2005). On other hand, in Drosophila, calcineurin, a Ca²⁺/calmodulin-dependent serine/threonine phosphatase, also controls the stability of clock proteins at the posttranslational level (Kweon et al., 2018). In particular, a null mutant of sarah, a calcineurin regulator, reduces the levels of TIM (also a canonical clock protein in Drosophila) and PER proteins in head extracts but not those of their respective transcripts. Of note, the effect of calcineurin on clock proteins levels is abolished when the proteasomal machinery is inhibited (Kweon et al., 2018), suggesting that in Drosophila, calcineurin regulates the core clock mechanism by protecting PER and TIM from proteasomal degradation.

Collectively, these findings demonstrate that the role of Ca²⁺ signaling is not limited to transducing the actions of external inputs within circadian pacemakers. Instead, studies in mammals and flies show that PKC, CaMK, calmodulin, and calcineurin, are integral components of clocks’ transcriptional and posttranslational feedback loops (Figures 1C,D). How is circadian rhythmicity decoded by these signaling protein? Here, we propose a model in which the oscillations of free Ca²⁺ in the cytoplasm impose a daily rhythm to the activity of its associated proteins (Figure 1). Thus, Ca²⁺ and its signaling pathways may regulate the molecular machinery of pacemaker cells and, consequently, also the periodicity of the resulting circadian behavior.

Circadian Regulation of Ca²⁺ Associated Proteins

Rhythmic Expression of Genes Coding for Proteins Associated With Ca²⁺ Pathways

In animals, the core molecular clock machinery directly or indirectly controls the expression of multiple downstream genes involved in the generation of rhythmic cellular process and circadian behaviors. Interestingly, in both mammals and Drosophila, a number of genes coding for proteins associated with Ca²⁺ pathways exhibit rhythmic transcription within a variety of biological clocks. For example, microarray and high throughput RNAseq analyses of mouse SCN reveal that genes that code for key proteins in Ca²⁺ signaling pathways such as camkii, pkc-α, and calcineurin, are under circadian control (Table 1) (Panda et al., 2002; Pembroke et al., 2015). These findings are consistent with previous studies that demonstrate that PKC activity shows a daily rhythm in SCN cells lines (Rivera-Bermudez et al., 2003) and that CaMKII is rhythmically expressed in the hamster central pacemaker (Agostino et al., 2004). In mice, canonical endoplasmic reticulum Ca²⁺ transporters (serca, ip₃r, and ryr) also exhibit circadian regulation at the transcriptional level in the SCN (Table 1). Interestingly, the contribution of the RyR to the phase-shifting mediated by light in the central clock is restricted to the early night (Ding et al., 1998), which in the mouse coincides with the time of peak protein levels in SCN [Table 1 and (Pfeffer et al., 2009)] and, as a result, cytosolic Ca²⁺ reaches high enough levels to phase shift the core molecular clock. Importantly, in mice, the promotor regions of camkii, pkcα, serca, ip₃r, and ryr, include E-BOX and ROREs motifs (consensus sequences for transcriptional regulation mediated by core clock components) (Table 1), suggesting that the rhythmic oscillation in mRNA levels of these genes may result from a direct regulation by the molecular machinery of the clock. Indeed, a deletion in a promotor region of ryr2 that includes the E-box sequence, reduces the transcriptional activation induced by the BMAL1-CLOCK complex in a mouse fibroblast cell line (Pfeffer et al., 2009), supporting the idea that the molecular clockwork can directly influence Ca²⁺ signaling.

TABLE 1

Table 1. Circadian regulation of genes coding for proteins associated with Ca²⁺ signaling in mice.

In mammals, the central clock can regulate Ca²⁺ influx from the extracellular milieu via voltage-gated Ca²⁺ channels (VGCCs). Indeed, in the SCN, some VGCCs subunits mediate the phase shifting induced by photic inputs as well as the daily changes in conductance (Colwell, 2011). In addition, L-type, T-type, and P/Q type VGCCs, are under circadian control at the transcriptional level in the rat SCN (Nahm et al., 2005). Interestingly, the rhythmic expression of L-type Ca²⁺ channels, the most abundant VGCCs in the SCN, is regulated by the circadian clock component, REV-ERBα (Schmutz et al., 2014). In particular, in mouse hypothalamic tissues (including the SCN), REV-ERBα binds to the promotor region of an L-type Ca²⁺ channel (Cacna1c) at ROREs and direct mutagenesis of this sequence abolishes the oscillation of Cacna1c mRNA levels, indicating that REV-ERBα plays a critical role in this circadian regulation. Of note, this mechanism is not the only one that has been associated with the rhythmic control of expression of L-type VGGCs. Indeed, in chicken cone photoreceptors, L-type-VGCCα1Cs display a diurnal rhythm of expression, which is controlled at the posttranscriptional level by microRNAs (Shi et al., 2009). In particular, in the retina, microRNA-26a exhibits a rhythmic expression and binds to the untranslated region of an L-type-VGGCα1C during the subjective day, thereby imposing a rhythm to the translation of this Ca²⁺ channel. Although there is evidence that microRNAs participate in the circadian control of transcription in the mammalian central clock (Cheng et al., 2007), it is still unknown whether they act at the posttranscriptional level on genes encoding proteins associated with Ca²⁺ signaling.

Another interesting case of circadian transcriptional regulation involving Ca²⁺ pathway proteins occurs in the Drosophila central clock. The adult fly brain has around 150 clock neurons per hemisphere, which are classified based on their anatomical location (Helfrich-Forster et al., 2007). These include so-called lateral (LN) and dorsal (DN) clusters of neurons (each of which can be further classified into subclusters), and a recent study using RNA-seq showed that each subcluster exhibits a different transcriptional profile (Abruzzi et al., 2017). Interestingly, a number of genes that are differentially expressed encode proteins of the Ca²⁺ pathway. For instance, dorsal lateral pacemaker neurons (LNds) (but not ventral lateral pacemaker neurons, LNvs), display a rhythmic expression in members of the PKC pathway (norpA, pkc53E, pkc98-E, and pkcα), and in genes encoding Ca²⁺ channels (cacophony, Ca^{2 +} α 1D) and genes involved in Ca²⁺ signaling (CaMK, calcineurin) (Table 2). Many of these genes contain E-box or RORE sequences in their promotor region, suggesting that the circadian transcriptional control is directly mediated by core clock components (Table 2). However, although LNd and DN1 neurons exhibit a similar circadian pattern of expression of genes encoding Ca²⁺-associated proteins, the spatiotemporal patterns of Ca²⁺ activity of LNds vs. DN1s are quite different (Liang et al., 2016) (see Figure 2 in Kozlov and Nagoshi, 2019), suggesting the existence of additional levels of regulation. What could be the underlying molecular mechanism? Wang et al. (2018) evaluated the alternative pre-mRNA splicing in Drosophila clock neurons, which is recognized as a major mechanism used to diversify the neuronal proteome. Combining RNAseq and computational methods, these authors quantified and categorized pre-mRNAs in pacemaker cells observing that each subgroup of pacemaker neurons possesses a unique alternative splicing profile. Of note, many transcripts of the Ca²⁺-calmodulin-dependent family of protein kinases, PKC signaling, and Ca²⁺ channels, were differentially enriched in DN1 vs. LNd pacemaker neurons, suggesting that posttranscriptional regulation may be critical for differentiating the roles of each circadian neuronal cluster in order to produce a functional circadian clock.

TABLE 2

Table 2. Circadian regulation of genes coding for proteins associated with Ca²⁺ signaling in Drosophila.

Skeletal Muscle and Heart, Two Peripherals Clocks Displaying Rhythmic Changes in the Transcription of Elements of the Ca²⁺ Signaling Pathway

Ca²⁺ pathways are fundamental to the functioning of some mammalian peripheral clocks. One of them is in the skeletal muscle, in which clock genes are necessary for maintaining its phenotype and metabolic homeostasis (Lefta et al., 2011). In rodents, 3–16% of the skeletal muscle transcriptome exhibits a circadian oscillation and many of these genes code for proteins involved in Ca²⁺ signaling (McCarthy et al., 2007; Dyar et al., 2014). For instance, a microarray study evaluated the transcriptomic profile of hindlimb leg muscle in adult mice and observed rhythmic expression in Ca²⁺-calmodulin-dependent protein kinases (camk, cask), the Ca²⁺ transporter of the sarcoplasmic reticulum (serca), and the Ca²⁺ buffer protein, parvalbumin, which did not occur in the muscles of CLOCK-knockout mice (McCarthy et al., 2007). Similar results have recently been described for human primary myoblasts with reduced expression of CLOCK (Perrin et al., 2018). Interestingly, the hindlimb muscles of a muscle-specific BMAL1 knockout mouse continue to exhibit a significant proportion of cycling genes, and, when they are denervated, 15% of the genes then lose their rhythmic expression (Dyar et al., 2015). These findings suggest that extracellular signals –probably originating from the SCN–play a major role in imposing a daily oscillation to the skeletal muscle transcriptome. Importantly, the changes in gene expression that are dependent on innervation are mediated by Ca²⁺ signaling. Indeed, RNAseq data reveal that, in the mouse soleus, a slow muscle fiber, one of the circadian pathways that is enriched in response to nerve activity is the Ca²⁺-calcineurin-NFAT pathway (Dyar et al., 2015). Importantly, NFAT is a transcription factor with a key role in muscle adaptation in response to physical activity (Akimoto et al., 2005). NFAT translocates to the nucleus in a circadian manner, leading to the rhythmic expression of genes such as rcan1, a typical reporter of the Ca²⁺-calcineurin-NFAT axis, thus revealing that this signaling pathway plays a critical role in integrating external stimuli with cycling gene expression (Dyar et al., 2015).

The heart is another peripheral clock whose functioning is highly dependent on a rhythmic Ca²⁺ pathway. Indeed, Ca²⁺ homeostasis is fundamental to the functioning of the heart and alterations in Ca²⁺ signaling are associated with a variety of cardiac pathologies (Bers, 2014). In addition, the circadian clock is critical in order for myocytes to maintain their contractile and metabolic function. As a result, in rodents, for example, cardiac muscle cells exhibit rhythmic expression in many genes including those that code for proteins of the Ca²⁺ signaling pathway (Bray et al., 2008; Sachan et al., 2011). In particular, in the mouse, muscles of the left ventricle exhibit a daily rhythm in the translocation of NFAT into the nucleus and, as a result, also in RCAN1 expression (Sachan et al., 2011). Importantly, this effect is abolished by calcineurin inhibitors, indicating that the Ca²⁺/calcineurin/NFAT axis has rhythmic activity. Additionally, the functioning of SERCA is also under circadian control in mouse myocytes. In particular, phosphorylation of phospholamban (a SERCA inhibitory signaling protein) is restricted to the early part of the night, which prevents it from binding to SERCA (Sachan et al., 2011), thereby allowing the entry of Ca²⁺ into the endoplasmic reticulum in a circadian manner (Sachan et al., 2011).

Collectively, current evidence reveals that Ca²⁺ modulates the expression of clock genes and is in turn modulated directly or indirectly by the molecular clock machinery (Figure 2B). This relationship results in a rhythm of cytosolic Ca²⁺ levels and of its downstream effectors. As a result, Ca²⁺ signaling and core molecular clock components maintain a reciprocal relationship that is important for the proper functioning of biological clocks as well as for that of the underlying circadian regulation of physiology (see Graphical Abstract).

Ca²⁺ Signaling and Clocks: Implications for Diseases and Chronomedicine

Circadian Ca²⁺ Signaling and Diseases

In humans, circadian clocks impose a daily rhythm to many physiological processes and behaviors including sleep, blood hormone levels, locomotor activity, body core temperature, and metabolism (Levi and Schibler, 2007). In several neurological disorders, patients exhibit alterations in their circadian rhythms, which are associated with changes in the expression of core clock components. Such is the case for schizophrenia, depression, Parkinson’s disease (PD), and Alzheimer disease (AD), where patients display altered sleep, and melatonin and core body temperature rhythms, due to alterations in clock gene expression and the loss of synchronization among pacemaker cells in the SCN (Videnovic et al., 2014; Musiek and Holtzman, 2016). Similarly, a dysfunction in the circadian clock is linked with the pathogenesis of various types of human cancers (Sancar and van Gelder, 2021). What molecular mechanisms could link the disruption of circadian rhythms to the development of these diseases? As we discussed above, PKC and CaMK are integral components of the molecular clock and, remarkably, abnormalities in the activity of these proteins have been described in the early stages of disorders that are associated with disturbances in clock function. For instance, higher levels or abnormal activity of PKC and CaMK isozymes leads to neuronal cell death and a disruption in neuronal transmission in PD, AD, and in neuropsychiatric disorders (Mochly-Rosen et al., 2012; Robison, 2014). Similarly, PKC overexpression promotes angiogenesis and excessive cell proliferation in stomach, colon, and breast cancers (Mochly-Rosen et al., 2012). Thus, in these disorders, abnormal CaMK or PKC signaling may alter the functioning of circadian TTFLs of both central and peripherals clocks, leading to a disruption in the rhythm of a variety of behavioral and physiological processes. In fact, a recent review suggests that a dysfunction in the clock system may be causal of neurodegeneration and that the pharmacological regulation of TTFLs could improve clinical outcomes (Cederroth et al., 2019). Consistently, a variety of psychotropic and cancer chemopreventive agents act by modulating CaMK and PKC activity, respectively, (Celano et al., 2003; Mochly-Rosen et al., 2012). Thus, recovering the normal functioning of the circadian clocks could have important implications for the effectiveness of these treatments. Thus, future studies may focus on elucidating whether these Ca²⁺-associated proteins mediate the link between the disruption of circadian clocks and the pathogenesis of neurological disorders and cancer.

Ca²⁺ channels also play a role in neurological disorders that cause alterations in circadian rhythms. One of them is bipolar disorder (BD), which is characterized by mood instability and abnormalities in sleep and daily activity schedules (bedtime, waketime, and mealtime) (Alloy et al., 2017). In BD, lithium is the most effective mood stabilizer and corrects daily rhythms, but not all patients are responsive to this treatment (Alda, 2015). In particular, BD patients with longer circadian periodicities do not respond to lithium and exhibit a greater polypharmacy (Sanghani et al., 2020). Additionally, mice with a dysfunctional clock do not display typical lithium-induced behavioral changes. These findings suggest that in BD patients the mood stabilizing effects of lithium could be mediated by the circadian clock. Conversely, several variants of genes coding for proteins of the Ca²⁺ pathways including cacna1c (L-type VGCC) are risk alleles for BD (Gershon et al., 2014; Ament et al., 2015). Interestingly, fibroblasts from healthy humans, but not from BD patients, exhibit a rhythm in cacna1c expression, and the inactivation of this Ca²⁺ channel prevents lithium from increasing the amplitude of circadian rhythms (McCarthy et al., 2016). But VGCCs are not the only components of Ca²⁺ pathways that are relevant to the lithium-induced circadian response in BD patients. In particular, lithium lengthens the circadian period in cultured cells, which does not occur in the presence of an IP₃R antagonist (McCarthy et al., 2019). In agreement with the potential role of IP₃R, an allelic variant of this Ca²⁺ transporter potentiates the lithium-induced period lengthening in BD patient-derived fibroblasts, suggesting that a genetic factor in Ca²⁺ signaling could influence the circadian defects seen in BD patients (McCarthy et al., 2019). Given that the effects of lithium on the clock appear to correlate with its effectiveness in mood stabilization of BD patients (Sanghani et al., 2020), considering the allelic variants of Ca²⁺ signaling could be important for implementing personalized medicine that improves the effectiveness of BD treatments.

Implications of Ca²⁺ Signaling in Chronomedicine

In recent years, a growing number of studies have documented time of day effects in the effectiveness of medical interventions. Indeed, such variations have been reported for the success of treatments such as chemotherapy (Sancar and van Gelder, 2021), as well as in the efficacy of drugs used to treat several disease including hypertension, cancer, hypercholesterolemia, rheumatoid arthritis, allergies, sleep disturbances, and asthma (Cederroth et al., 2019). One explanation for this is that many of drugs have short half-lives and their targets exhibit circadian expression. For instance, in non-human primates, about 80% of protein-coding genes display a daily rhythm of expression and a large proportion of these genes are identified as drug targets by the United States Food and Drug Administration (Mure et al., 2018). Similarly, a genome-wide transcriptome study in humans identified thousands of genes with tissue-specific circadian expression in 13 different organs (Ruben et al., 2018). A notable example is the various L-type Ca²⁺ channel subunits, which display a rhythmic expression in the heart (Table 3 and Figure 3) suggesting that their sensitivity to drugs would vary during the course of the day. And indeed, nifedipine and verapamil, two Ca²⁺ channels blockers used as antihypertensive drugs, show an improved efficacy when administered before bedtime (White et al., 1995; Hermida et al., 2008). In addition, a variety of Ca²⁺ channels blockers have half-lives <6 h (Elliott and Ram, 2011) suggesting that taking these drugs at peak times of Ca²⁺ channel expression could improve the efficacy of the pharmacological therapy (this could also reduce side effects caused by actions on other tissues where the relevant targets cycle with a different phase). Consistent with this hypothesis, harmonizing the timing of administration of a drug with the time of peak expression of its target improves the effectiveness of treatments for cardiovascular disease, hypercholesterolemia, and obesity (Awad et al., 2017). On other hand, a circadian database generated by Ruben et al. (2018) shows that many genes encoding Ca²⁺ signaling proteins show daily rhythms of expression in a variety of peripheral clocks (Figure 3), which is consistent with previous transcriptomic analyses of different tissues and brain regions of mice (Zhang et al., 2014) and baboons (Mure et al., 2018). Thus, taking into account the daily changes in the abundance of these drug targets may have significant implications for medicine because proteins from the Ca²⁺ pathway are therapeutic targets in multiple disorders. For instance, the SERCA inhibitor prodrug, mipsagargin, is being assessed in clinical trials for the treatment of various types of cancers including prostate and liver (Mahalingam et al., 2016; Mahalingam et al., 2019). Similarly, recent pre-clinical studies propose that the RyR antagonist, dantrolene, would have a neuroprotective role in Huntington and Alzheimer’s models (Chen et al., 2011; Liang and Wei, 2015).

TABLE 3

Table 3. Drugs targeting elements of the Ca²⁺ signaling pathway and their usage in medicine.

FIGURE 3

Figure 3. Rhythmic expression of components of the Ca²⁺ signaling pathway in human tissues. Schematic showing tissue-specific circadian expression of Ca²⁺-associated proteins and of Ca²⁺ channels and transporters in peripheral human tissues. Based on data from Ruben et al. (2018) (http://circadb.hogeneschlab.org/human).

Considering the daily changes in Ca²⁺ signaling may be relevant not only for deciding on the best time for drug administration but also for scheduling medical interventions. For example, in humans, a common outcome of cardiac surgery is myocardial injury due to ischemia-reperfusion (I/R) (Hausenloy and Yellon, 2016). A recent study in humans, revealed that the injury by I/R following aortic valve replacement is greatest when the surgery is done in the morning compared to the evening. This difference in the time of the day is abolished in a mouse model of hypoxia/reoxygenation treated with Rev-ERBα antagonists, suggesting a critical role of this circadian clock component in the myocardial tolerance to I/R (Montaigne et al., 2018). Interestingly, this circadian regulation would not only be controlled by Rev-ERBα but also by the calcineurin/rcan1 axis. As we discussed above, in mice, the heart calcineurin/NFAT/Rcan1 pathway displays rhythmic activity (Sachan et al., 2011) and, remarkably, this process could influence the daily variations in the myocardial tolerance to I/R. Unlike the findings reported by Montaigne et al. (2018), injury by I/R following coronary artery surgery in mice is greater in animals operated at the end of their active phase compared to those operated at the beginning of this phase (Rotter et al., 2014). This time of day difference in tolerance to I/R is not present in Rcan1 knockout mice (Rotter et al., 2014). Since these mutant mice display a rhythmic expression in canonical clock genes in the heart, these results suggest that Rcan1 mediates this effect without altering the global functioning of this peripheral clock. In addition, inhibiting calcineurin activity decreases the severity of the I/R injury in animals operated at PM whereas it does not confer additional protection in AM-operated mice, supporting the idea that the calcineurin/Rcan1 pathway plays a key role in determining the time of day-dependent susceptibility of the heart to I/R. Even though additional studies are needed to elucidate whether a similar regulation occurs in humans, this finding positions the calcineurin/rcan1 axis as a therapeutic target for cardioprotection and for blunting the effect of the time of day on the outcome of cardiac surgery.

Collectively these findings provide strong evidence that the circadian control of Ca²⁺ signaling in biological clocks may have significant implications for medicine (Table 3). Thus, taking the 24-h dynamics of Ca²⁺ signaling into account in pharmacological therapies and medical interventions could improve drug efficacy and postoperative clinical outcomes, supporting the emerging idea that circadian biology should be an integral part of translational research (Cederroth et al., 2019).

Closing Remarks

We currently have a very detailed understanding of how circadian clocks function. By comparison, much less is known about how they are synchronized and coordinated; how they transmit time information to the host; and, in turn, how they can be affected by the host’s physiology and behavior. All of these system-level functions ultimately converge on intracellular signals that affect gene expression, which, in turn, alter the activity of clocks, and the physiology of cells, organs, and organisms. Future work aimed at increasing our knowledge on how intracellular signaling regulates, and is regulated, by clocks will be important for furthering our understanding of how this intricate network of interactions is effected and how a unified time for the organism is maintained yet can be modulated by the host. It will also be critical for the development of more effective chronomedicine prescriptions aimed at improving the effectiveness of drugs while reducing their negative and off-target effects.

Author Contributions

JC-L wrote the first draft. JC-L and JE edited manuscript. Both authors contributed to the article and approved the submitted version.

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.

Funding

This work was supported by ANID Graduate Fellowship #21180133 (to JC-L); FONDECYT (National Fund for Scientific and Technological Development, Chile) grant #1180403 (to JE); and the ANID – Millennium Science Initiative Program “Centro Interdisciplinario de Neurociencia de Valparaiso (CINV)” grant P09-022-F (to JE).

References

Abruzzi, K. C., Zadina, A., Luo, W., Wiyanto, E., Rahman, R., Guo, F., et al. (2017). RNA-seq analysis of Drosophila clock and non-clock neurons reveals neuron-specific cycling and novel candidate neuropeptides. PLoS Genet. 13:e1006613. doi: 10.1371/journal.pgen.1006613

PubMed Abstract | CrossRef Full Text | Google Scholar

Agostino, P. V., Ferreyra, G. A., Murad, A. D., Watanabe, Y., and Golombek, D. A. (2004). Diurnal, circadian and photic regulation of calcium/calmodulin-dependent kinase II and neuronal nitric oxide synthase in the hamster suprachiasmatic nuclei. Neurochem. Int. 44, 617–625. doi: 10.1016/j.neuint.2003.09.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Aguilar-Roblero, R., Mercado, C., Alamilla, J., Laville, A., and Diaz-Munoz, M. (2007). Ryanodine receptor Ca2+-release channels are an output pathway for the circadian clock in the rat suprachiasmatic nuclei. Eur. J. Neurosci. 26, 575–582. doi: 10.1111/j.1460-9568.2007.05679.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Akashi, M., Tsuchiya, Y., Yoshino, T., and Nishida, E. (2002). Control of intracellular dynamics of mammalian period proteins by casein kinase I epsilon (CKIepsilon) and CKIdelta in cultured cells. Mol. Cell. Biol. 22, 1693–1703. doi: 10.1128/mcb.22.6.1693-1703.2002

PubMed Abstract | CrossRef Full Text | Google Scholar

Akimoto, T., Pohnert, S. C., Li, P., Zhang, M., Gumbs, C., Rosenberg, P. B., et al. (2005). Exercise stimulates Pgc-1alpha transcription in skeletal muscle through activation of the p38 MAPK pathway. J. Biol. Chem. 280, 19587–19593. doi: 10.1074/jbc.m408862200

PubMed Abstract | CrossRef Full Text | Google Scholar

Alda, M. (2015). Lithium in the treatment of bipolar disorder: pharmacology and pharmacogenetics. Mol. Psychiatry 20, 661–670. doi: 10.1038/mp.2015.4

PubMed Abstract | CrossRef Full Text | Google Scholar

Alloy, L. B., Ng, T. H., Titone, M. K., and Boland, E. M. (2017). Circadian rhythm dysregulation in bipolar spectrum disorders. Curr. Psychiatry Rep. 19:21.

Google Scholar

Ament, S. A., Szelinger, S., Glusman, G., Ashworth, J., Hou, L., Akula, N., et al. (2015). Rare variants in neuronal excitability genes influence risk for bipolar disorder. Proc. Natl. Acad. Sci. U.S.A. 112, 3576–3581. doi: 10.1073/pnas.1424958112

PubMed Abstract | CrossRef Full Text | Google Scholar

Ampleford, E. J., and Steel, C. G. (1985). Circadian control of a daily rhythm in hemolymph ecdysteroid titer in the insect Rhodnius prolixus (Hemiptera). Gen. Comp. Endocrinol. 59, 453–459. doi: 10.1016/0016-6480(85)90404-6

CrossRef Full Text | Google Scholar

Awad, K., Serban, M. C., Penson, P., Mikhailidis, D. P., Toth, P. P., Jones, S. R., et al. (2017). Effects of morning vs evening statin administration on lipid profile: a systematic review and meta-analysis. J. Clin. Lipidol. 11, 972– 985.e9.

Google Scholar

Baez-Ruiz, A., and Diaz-Munoz, M. (2011). Chronic inhibition of endoplasmic reticulum calcium-release channels and calcium-ATPase lengthens the period of hepatic clock gene Per1. J. Circadian Rhythms 9:6. doi: 10.1186/1740-3391-9-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Bers, D. M. (2014). Cardiac sarcoplasmic reticulum calcium leak: basis and roles in cardiac dysfunction. Annu. Rev. Physiol. 76, 107–127. doi: 10.1146/annurev-physiol-020911-153308

PubMed Abstract | CrossRef Full Text | Google Scholar

Brancaccio, M., Maywood, E. S., Chesham, J. E., Loudon, A. S., and Hastings, M. H. (2013). A Gq-Ca2+ axis controls circuit-level encoding of circadian time in the suprachiasmatic nucleus. Neuron 78, 714–728. doi: 10.1016/j.neuron.2013.03.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Brancaccio, M., Patton, A. P., Chesham, J. E., Maywood, E. S., and Hastings, M. H. (2017). Astrocytes control circadian timekeeping in the suprachiasmatic nucleus via glutamatergic signaling. Neuron 93, 1420–1435.e5.

Google Scholar

Bray, M. S., Shaw, C. A., Moore, M. W., Garcia, R. A., Zanquetta, M. M., Durgan, D. J., et al. (2008). Disruption of the circadian clock within the cardiomyocyte influences myocardial contractile function, metabolism, and gene expression. Am. J. Physiol. Heart Circ. Physiol. 294, H1036–H1047.

Google Scholar

Cederroth, C. R., Albrecht, U., Bass, J., Brown, S. A., Dyhrfjeld-Johnsen, J., Gachon, F., et al. (2019). Medicine in the fourth dimension. Cell Metab. 30, 238–250.

Google Scholar

Celano, E., Tiraboschi, E., Consogno, E., D’urso, G., Mbakop, M. P., Gennarelli, M., et al. (2003). Selective regulation of presynaptic calcium/calmodulin-dependent protein kinase II by psychotropic drugs. Biol. Psychiatry 53, 442–449. doi: 10.1016/s0006-3223(02)01491-9

CrossRef Full Text | Google Scholar

Chen, X., Wu, J., Lvovskaya, S., Herndon, E., Supnet, C., and Bezprozvanny, I. (2011). Dantrolene is neuroprotective in Huntington’s disease transgenic mouse model. Mol. Neurodegener. 6:81. doi: 10.1186/1750-1326-6-81

PubMed Abstract | CrossRef Full Text | Google Scholar

Cheng, H. Y., Papp, J. W., Varlamova, O., Dziema, H., Russell, B., Curfman, J. P., et al. (2007). microRNA modulation of circadian-clock period and entrainment. Neuron 54, 813–829. doi: 10.1016/j.neuron.2007.05.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Colwell, C. S. (2000). Circadian modulation of calcium levels in cells in the suprachiasmatic nucleus. Eur. J. Neurosci. 12, 571–576. doi: 10.1046/j.1460-9568.2000.00939.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Colwell, C. S. (2011). Linking neural activity and molecular oscillations in the SCN. Nat. Rev. Neurosci. 12, 553–569. doi: 10.1038/nrn3086

PubMed Abstract | CrossRef Full Text | Google Scholar

Colwell, C. S., Whitmore, D., Michel, S., and Block, G. D. (1994). Calcium plays a central role in phase shifting the ocular circadian pacemaker of Aplysia. J. Comp. Physiol. A 175, 415–423.

Google Scholar

Damiola, F., Le Minh, N., Preitner, N., Kornmann, B., Fleury-Olela, F., and Schibler, U. (2000). Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus. Genes Dev. 14, 2950–2961. doi: 10.1101/gad.183500

PubMed Abstract | CrossRef Full Text | Google Scholar

Depetris-Chauvin, A., Berni, J., Aranovich, E. J., Muraro, N. I., Beckwith, E. J., and Ceriani, M. F. (2011). Adult-specific electrical silencing of pacemaker neurons uncouples molecular clock from circadian outputs. Curr. Biol. 21, 1783–1793. doi: 10.1016/j.cub.2011.09.027

PubMed Abstract | CrossRef Full Text | Google Scholar

Ding, J. M., Buchanan, G. F., Tischkau, S. A., Chen, D., Kuriashkina, L., Faiman, L. E., et al. (1998). A neuronal ryanodine receptor mediates light-induced phase delays of the circadian clock. Nature 394, 381–384. doi: 10.1038/28639

PubMed Abstract | CrossRef Full Text | Google Scholar

Dyar, K. A., Ciciliot, S., Tagliazucchi, G. M., Pallafacchina, G., Tothova, J., Argentini, C., et al. (2015). The calcineurin-NFAT pathway controls activity-dependent circadian gene expression in slow skeletal muscle. Mol. Metab. 4, 823–833. doi: 10.1016/j.molmet.2015.09.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Dyar, K. A., Ciciliot, S., Wright, L. E., Bienso, R. S., Tagliazucchi, G. M., Patel, V. R., et al. (2014). Muscle insulin sensitivity and glucose metabolism are controlled by the intrinsic muscle clock. Mol. Metab. 3, 29–41. doi: 10.1016/j.molmet.2013.10.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Eide, E. J., Woolf, M. F., Kang, H., Woolf, P., Hurst, W., Camacho, F., et al. (2005). Control of mammalian circadian rhythm by CKIepsilon-regulated proteasome-mediated PER2 degradation. Mol. Cell. Biol. 25, 2795–2807. doi: 10.1128/mcb.25.7.2795-2807.2005

PubMed Abstract | CrossRef Full Text | Google Scholar

Elliott, W. J., and Ram, C. V. (2011). Calcium channel blockers. J. Clin. Hypertens. (Greenwich) 13, 687–689. doi: 10.1111/j.1751-7176.2011.00513.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Enoki, R., Kuroda, S., Ono, D., Hasan, M. T., Ueda, T., Honma, S., et al. (2012). Topological specificity and hierarchical network of the circadian calcium rhythm in the suprachiasmatic nucleus. Proc. Natl. Acad. Sci. U.S.A. 109, 21498–21503. doi: 10.1073/pnas.1214415110

PubMed Abstract | CrossRef Full Text | Google Scholar

Enoki, R., Ono, D., Kuroda, S., Honma, S., and Honma, K. I. (2017). Dual origins of the intracellular circadian calcium rhythm in the suprachiasmatic nucleus. Sci. Rep. 7:41733.

Google Scholar

Gallego, M., and Virshup, D. M. (2007). Post-translational modifications regulate the ticking of the circadian clock. Nat. Rev. Mol. Cell Biol. 8, 139–148. doi: 10.1038/nrm2106

PubMed Abstract | CrossRef Full Text | Google Scholar

Gershon, E. S., Grennan, K., Busnello, J., Badner, J. A., Ovsiew, F., Memon, S., et al. (2014). A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain. Mol. Psychiatry 19, 890–894. doi: 10.1038/mp.2013.107

PubMed Abstract | CrossRef Full Text | Google Scholar

Ginty, D. D., Kornhauser, J. M., Thompson, M. A., Bading, H., Mayo, K. E., Takahashi, J. S., et al. (1993). Regulation of CREB phosphorylation in the suprachiasmatic nucleus by light and a circadian clock. Science 260, 238–241. doi: 10.1126/science.8097062

PubMed Abstract | CrossRef Full Text | Google Scholar

Guo, F., Chen, X., and Rosbash, M. (2017). Temporal calcium profiling of specific circadian neurons in freely moving flies. Proc. Natl. Acad. Sci. U.S.A. 114, E8780–E8787.

Google Scholar

Hablitz, L. M., Gunesch, A. N., Cravetchi, O., Moldavan, M., and Allen, C. N. (2020). Cannabinoid signaling recruits astrocytes to modulate presynaptic function in the suprachiasmatic nucleus. eNeuro 7:ENEURO.0081-19.2020.

Google Scholar

Hanauer, S. B. (2008). The role of loperamide in gastrointestinal disorders. Rev. Gastroenterol. Disord. 8, 15–20.

Google Scholar

Hao, H., Allen, D. L., and Hardin, P. E. (1997). A circadian enhancer mediates PER-dependent mRNA cycling in Drosophila melanogaster. Mol. Cell. Biol. 17, 3687–3693. doi: 10.1128/mcb.17.7.3687

PubMed Abstract | CrossRef Full Text | Google Scholar

Hardin, P. E. (2011). Molecular genetic analysis of circadian timekeeping in Drosophila. Adv. Genet. 74, 141–173. doi: 10.1016/b978-0-12-387690-4.00005-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Harrisingh, M. C., Wu, Y., Lnenicka, G. A., and Nitabach, M. N. (2007). Intracellular Ca2+ regulates free-running circadian clock oscillation in vivo. J. Neurosci. 27, 12489–12499. doi: 10.1523/jneurosci.3680-07.2007

PubMed Abstract | CrossRef Full Text | Google Scholar

Hasan, M., Pulman, J., and Marson, A. G. (2013). Calcium antagonists as an add-on therapy for drug-resistant epilepsy. Cochrane Database Syst. Rev. 2013:CD002750.

Google Scholar

Hausenloy, D. J., and Yellon, D. M. (2016). Ischaemic conditioning and reperfusion injury. Nat. Rev. Cardiol. 13, 193–209. doi: 10.1038/nrcardio.2016.5

PubMed Abstract | CrossRef Full Text | Google Scholar

Helfrich-Forster, C., Shafer, O. T., Wulbeck, C., Grieshaber, E., Rieger, D., and Taghert, P. (2007). Development and morphology of the clock-gene-expressing lateral neurons of Drosophila melanogaster. J. Comp. Neurol. 500, 47–70. doi: 10.1002/cne.21146

PubMed Abstract | CrossRef Full Text | Google Scholar

Hermida, R. C., Ayala, D. E., Mojon, A., and Fernandez, J. R. (2008). Chronotherapy with nifedipine GITS in hypertensive patients: improved efficacy and safety with bedtime dosing. Am. J. Hypertens. 21, 948–954. doi: 10.1038/ajh.2008.216

PubMed Abstract | CrossRef Full Text | Google Scholar

Huang, X., Warren, J. T., and Gilbert, L. I. (2008). New players in the regulation of ecdysone biosynthesis. J. Genet. Genomics 35, 1–10. doi: 10.1016/s1673-8527(08)60001-6

CrossRef Full Text | Google Scholar

Hyun, S., Lee, Y., Hong, S. T., Bang, S., Paik, D., Kang, J., et al. (2005). Drosophila GPCR han is a receptor for the circadian clock neuropeptide PDF. Neuron 48, 267–278. doi: 10.1016/j.neuron.2005.08.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Ikeda, M., and Ikeda, M. (2014). Bmal1 is an essential regulator for circadian cytosolic Ca(2)(+) rhythms in suprachiasmatic nucleus neurons. J. Neurosci. 34, 12029–12038. doi: 10.1523/jneurosci.5158-13.2014

PubMed Abstract | CrossRef Full Text | Google Scholar

Ikeda, M., Sugiyama, T., Wallace, C. S., Gompf, H. S., Yoshioka, T., Miyawaki, A., et al. (2003). Circadian dynamics of cytosolic and nuclear Ca2+ in single suprachiasmatic nucleus neurons. Neuron 38, 253–263. doi: 10.1016/s0896-6273(03)00164-8

CrossRef Full Text | Google Scholar

Jakubcakova, V., Oster, H., Tamanini, F., Cadenas, C., Leitges, M., Van Der Horst, G. T., et al. (2007). Light entrainment of the mammalian circadian clock by a PRKCA-dependent posttranslational mechanism. Neuron 54, 831–843. doi: 10.1016/j.neuron.2007.04.031

PubMed Abstract | CrossRef Full Text | Google Scholar

Jones, J. R., Simon, T., Lones, L., and Herzog, E. D. (2018). SCN VIP neurons are essential for normal light-mediated resetting of the circadian system. J. Neurosci. 38, 7986–7995. doi: 10.1523/jneurosci.1322-18.2018

PubMed Abstract | CrossRef Full Text | Google Scholar

King, A. N., and Sehgal, A. (2020). Molecular and circuit mechanisms mediating circadian clock output in the Drosophila brain. Eur. J. Neurosci. 51, 268–281. doi: 10.1111/ejn.14092

PubMed Abstract | CrossRef Full Text | Google Scholar

Kon, N., Yoshikawa, T., Honma, S., Yamagata, Y., Yoshitane, H., Shimizu, K., et al. (2014). CaMKII is essential for the cellular clock and coupling between morning and evening behavioral rhythms. Genes Dev. 28, 1101–1110. doi: 10.1101/gad.237511.114

PubMed Abstract | CrossRef Full Text | Google Scholar

Kozlov, A., and Nagoshi, E. (2019). Decoding Drosophila circadian pacemaker circuit. Curr. Opin. Insect Sci. 36, 33–38. doi: 10.1016/j.cois.2019.06.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Krause, T., Gerbershagen, M. U., Fiege, M., Weisshorn, R., and Wappler, F. (2004). Dantrolene–a review of its pharmacology, therapeutic use and new developments. Anaesthesia 59, 364–373. doi: 10.1111/j.1365-2044.2004.03658.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Kweon, S. H., Lee, J., Lim, C., and Choe, J. (2018). High-amplitude circadian rhythms in Drosophila driven by calcineurin-mediated post-translational control of sarah. Genetics 209, 815–828. doi: 10.1534/genetics.118.300808

PubMed Abstract | CrossRef Full Text | Google Scholar

Lefta, M., Wolff, G., and Esser, K. A. (2011). Circadian rhythms, the molecular clock, and skeletal muscle. Curr. Top. Dev. Biol. 96, 231–271. doi: 10.1016/b978-0-12-385940-2.00009-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Levi, F., and Schibler, U. (2007). Circadian rhythms: mechanisms and therapeutic implications. Annu. Rev. Pharmacol. Toxicol. 47, 593–628. doi: 10.1146/annurev.pharmtox.47.120505.105208

PubMed Abstract | CrossRef Full Text | Google Scholar

Liang, L., and Wei, H. (2015). Dantrolene, a treatment for Alzheimer disease? Alzheimer Dis. Assoc. Disord. 29, 1–5. doi: 10.1097/wad.0000000000000076

PubMed Abstract | CrossRef Full Text | Google Scholar

Liang, X., Holy, T. E., and Taghert, P. H. (2016). Synchronous Drosophila circadian pacemakers display nonsynchronous Ca(2)(+) rhythms in vivo. Science 351, 976–981. doi: 10.1126/science.aad3997

PubMed Abstract | CrossRef Full Text | Google Scholar

Liang, X., Holy, T. E., and Taghert, P. H. (2017). A series of suppressive signals within the Drosophila circadian neural circuit generates sequential daily outputs. Neuron 94, 1173–1189.e4.

Google Scholar

Lundkvist, G. B., Kwak, Y., Davis, E. K., Tei, H., and Block, G. D. (2005). A calcium flux is required for circadian rhythm generation in mammalian pacemaker neurons. J. Neurosci. 25, 7682–7686. doi: 10.1523/jneurosci.2211-05.2005

PubMed Abstract | CrossRef Full Text | Google Scholar

Mahalingam, D., Peguero, J., Cen, P., Arora, S. P., Sarantopoulos, J., Rowe, J., et al. (2019). A phase II, multicenter, single-arm study of mipsagargin (G-202) as a second-line therapy following sorafenib for adult patients with progressive advanced hepatocellular carcinoma. Cancers (Basel) 11:833. doi: 10.3390/cancers11060833

PubMed Abstract | CrossRef Full Text | Google Scholar

Mahalingam, D., Wilding, G., Denmeade, S., Sarantopoulas, J., Cosgrove, D., Cetnar, J., et al. (2016). Mipsagargin, a novel thapsigargin-based PSMA-activated prodrug: results of a first-in-man phase I clinical trial in patients with refractory, advanced or metastatic solid tumours. Br. J. Cancer 114, 986–994. doi: 10.1038/bjc.2016.72

PubMed Abstract | CrossRef Full Text | Google Scholar

McCarthy, J. J., Andrews, J. L., Mcdearmon, E. L., Campbell, K. S., Barber, B. K., Miller, B. H., et al. (2007). Identification of the circadian transcriptome in adult mouse skeletal muscle. Physiol. Genomics 31, 86–95. doi: 10.1152/physiolgenomics.00066.2007

PubMed Abstract | CrossRef Full Text | Google Scholar

McCarthy, M. J., Le Roux, M. J., Wei, H., Beesley, S., Kelsoe, J. R., and Welsh, D. K. (2016). Calcium channel genes associated with bipolar disorder modulate lithium’s amplification of circadian rhythms. Neuropharmacology 101, 439–448. doi: 10.1016/j.neuropharm.2015.10.017

PubMed Abstract | CrossRef Full Text | Google Scholar

McCarthy, M. J., Wei, H., Nievergelt, C. M., Stautland, A., Maihofer, A. X., Welsh, D. K., et al. (2019). Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder. Neuropsychopharmacology 44, 620–628.

Google Scholar

McGivern, J. G. (2007). Ziconotide: a review of its pharmacology and use in the treatment of pain. Neuropsychiatr. Dis. Treat. 3, 69–85. doi: 10.2147/nedt.2007.3.1.69

PubMed Abstract | CrossRef Full Text | Google Scholar

Mizrak, D., Ruben, M., Myers, G. N., Rhrissorrakrai, K., Gunsalus, K. C., and Blau, J. (2012). Electrical activity can impose time of day on the circadian transcriptome of pacemaker neurons. Curr. Biol. 22, 1871–1880. doi: 10.1016/j.cub.2012.07.070

PubMed Abstract | CrossRef Full Text | Google Scholar

Mochly-Rosen, D., Das, K., and Grimes, K. V. (2012). Protein kinase C, an elusive therapeutic target? Nat. Rev. Drug Discov. 11, 937–957. doi: 10.1038/nrd3871

PubMed Abstract | CrossRef Full Text | Google Scholar

Mohawk, J. A., Green, C. B., and Takahashi, J. S. (2012). Central and peripheral circadian clocks in mammals. Annu. Rev. Neurosci. 35, 445–462. doi: 10.1146/annurev-neuro-060909-153128

PubMed Abstract | CrossRef Full Text | Google Scholar

Montaigne, D., Marechal, X., Modine, T., Coisne, A., Mouton, S., Fayad, G., et al. (2018). Daytime variation of perioperative myocardial injury in cardiac surgery and its prevention by Rev-Erbalpha antagonism: a single-centre propensity-matched cohort study and a randomised study. Lancet 391, 59–69. doi: 10.1016/s0140-6736(17)32132-3

CrossRef Full Text | Google Scholar

Morioka, E., Matsumoto, A., and Ikeda, M. (2012). Neuronal influence on peripheral circadian oscillators in pupal Drosophila prothoracic glands. Nat. Commun. 3:909.

Google Scholar

Mure, L. S., Le, H. D., Benegiamo, G., Chang, M. W., Rios, L., Jillani, N., et al. (2018). Diurnal transcriptome atlas of a primate across major neural and peripheral tissues. Science 359:eaao0318. doi: 10.1126/science.aao0318

PubMed Abstract | CrossRef Full Text | Google Scholar

Musiek, E. S., and Holtzman, D. M. (2016). Mechanisms linking circadian clocks, sleep, and neurodegeneration. Science 354, 1004–1008. doi: 10.1126/science.aah4968

PubMed Abstract | CrossRef Full Text | Google Scholar

Nahm, S. S., Farnell, Y. Z., Griffith, W., and Earnest, D. J. (2005). Circadian regulation and function of voltage-dependent calcium channels in the suprachiasmatic nucleus. J. Neurosci. 25, 9304–9308. doi: 10.1523/jneurosci.2733-05.2005

PubMed Abstract | CrossRef Full Text | Google Scholar

Nam, H. J., Boo, K., Kim, D., Han, D. H., Choe, H. K., Kim, C. R., et al. (2014). Phosphorylation of LSD1 by PKCalpha is crucial for circadian rhythmicity and phase resetting. Mol. Cell 53, 791–805. doi: 10.1016/j.molcel.2014.01.028

PubMed Abstract | CrossRef Full Text | Google Scholar

Noguchi, T., Leise, T. L., Kingsbury, N. J., Diemer, T., Wang, L. L., Henson, M. A., et al. (2017). Calcium circadian rhythmicity in the suprachiasmatic nucleus: cell autonomy and network modulation. eNeuro 4:ENEURO.0160-17.2017.

Google Scholar

Nomura, K., Takeuchi, Y., Yamaguchi, S., Okamura, H., and Fukunaga, K. (2003). Involvement of calcium/calmodulin-dependent protein kinase II in the induction of mPer1. J. Neurosci. Res. 72, 384–392. doi: 10.1002/jnr.10581

PubMed Abstract | CrossRef Full Text | Google Scholar

Ogueta, M., Hardie, R. C., and Stanewsky, R. (2018). Non-canonical phototransduction mediates synchronization of the Drosophila melanogaster circadian clock and retinal light responses. Curr. Biol. 28, 1725–1735.e3.

Google Scholar

Ogueta, M., Hardie, R. C., and Stanewsky, R. (2020). Light sampling via throttled visual phototransduction robustly synchronizes the Drosophila circadian clock. Curr. Biol. 30, 2551–2563.e3.

Google Scholar

Palacios-Munoz, A., and Ewer, J. (2018). Calcium and cAMP directly modulate the speed of the Drosophila circadian clock. PLoS Genet. 14:e1007433. doi: 10.1371/journal.pgen.1007433

PubMed Abstract | CrossRef Full Text | Google Scholar

Panda, S., Antoch, M. P., Miller, B. H., Su, A. I., Schook, A. B., Straume, M., et al. (2002). Coordinated transcription of key pathways in the mouse by the circadian clock. Cell 109, 307–320. doi: 10.1016/s0092-8674(02)00722-5

CrossRef Full Text | Google Scholar

Patke, A., Young, M. W., and Axelrod, S. (2020). Molecular mechanisms and physiological importance of circadian rhythms. Nat. Rev. Mol. Cell Biol. 21, 67–84. doi: 10.1038/s41580-019-0179-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Pembroke, W. G., Babbs, A., Davies, K. E., Ponting, C. P., and Oliver, P. L. (2015). Temporal transcriptomics suggest that twin-peaking genes reset the clock. Elife 4:e10518.

Google Scholar

Perrin, L., Loizides-Mangold, U., Chanon, S., Gobet, C., Hulo, N., Isenegger, L., et al. (2018). Transcriptomic analyses reveal rhythmic and CLOCK-driven pathways in human skeletal muscle. Elife 7:e34114.

Google Scholar

Pfeffer, M., Muller, C. M., Mordel, J., Meissl, H., Ansari, N., Deller, T., et al. (2009). The mammalian molecular clockwork controls rhythmic expression of its own input pathway components. J. Neurosci. 29, 6114–6123. doi: 10.1523/jneurosci.0275-09.2009

PubMed Abstract | CrossRef Full Text | Google Scholar

Preitner, N., Damiola, F., Lopez-Molina, L., Zakany, J., Duboule, D., Albrecht, U., et al. (2002). The orphan nuclear receptor REV-ERBalpha controls circadian transcription within the positive limb of the mammalian circadian oscillator. Cell 110, 251–260. doi: 10.1016/s0092-8674(02)00825-5

CrossRef Full Text | Google Scholar

Reischl, S., and Kramer, A. (2011). Kinases and phosphatases in the mammalian circadian clock. FEBS Lett. 585, 1393–1399. doi: 10.1016/j.febslet.2011.02.038

PubMed Abstract | CrossRef Full Text | Google Scholar

Rivera-Bermudez, M. A., Gerdin, M. J., Earnest, D. J., and Dubocovich, M. L. (2003). Regulation of basal rhythmicity in protein kinase C activity by melatonin in immortalized rat suprachiasmatic nucleus cells. Neurosci. Lett. 346, 37–40. doi: 10.1016/s0304-3940(03)00590-1

CrossRef Full Text | Google Scholar

Robison, A. J. (2014). Emerging role of CaMKII in neuropsychiatric disease. Trends Neurosci. 37, 653–662. doi: 10.1016/j.tins.2014.07.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Robles, M. S., Boyault, C., Knutti, D., Padmanabhan, K., and Weitz, C. J. (2010). Identification of RACK1 and protein kinase Calpha as integral components of the mammalian circadian clock. Science 327, 463–466. doi: 10.1126/science.1180067

PubMed Abstract | CrossRef Full Text | Google Scholar

Rotter, D., Grinsfelder, D. B., Parra, V., Pedrozo, Z., Singh, S., Sachan, N., et al. (2014). Calcineurin and its regulator, RCAN1, confer time-of-day changes in susceptibility of the heart to ischemia/reperfusion. J. Mol. Cell. Cardiol. 74, 103–111. doi: 10.1016/j.yjmcc.2014.05.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Ruben, M. D., Wu, G., Smith, D. F., Schmidt, R. E., Francey, L. J., Lee, Y. Y., et al. (2018). A database of tissue-specific rhythmically expressed human genes has potential applications in circadian medicine. Sci. Transl. Med. 10:eaat8806. doi: 10.1126/scitranslmed.aat8806

PubMed Abstract | CrossRef Full Text | Google Scholar

Sachan, N., Dey, A., Rotter, D., Grinsfelder, D. B., Battiprolu, P. K., Sikder, D., et al. (2011). Sustained hemodynamic stress disrupts normal circadian rhythms in calcineurin-dependent signaling and protein phosphorylation in the heart. Circ. Res. 108, 437–445. doi: 10.1161/circresaha.110.235309

PubMed Abstract | CrossRef Full Text | Google Scholar

Saint-Charles, A., Michard-Vanhee, C., Alejevski, F., Chelot, E., Boivin, A., and Rouyer, F. (2016). Four of the six Drosophila rhodopsin-expressing photoreceptors can mediate circadian entrainment in low light. J. Comp. Neurol. 524, 2828–2844. doi: 10.1002/cne.23994

PubMed Abstract | CrossRef Full Text | Google Scholar

Sancar, A., and van Gelder, R. N. (2021). Clocks, cancer, and chronochemotherapy. Science 371:eabb0738. doi: 10.1126/science.abb0738

PubMed Abstract | CrossRef Full Text | Google Scholar

Sanghani, H. R., Jagannath, A., Humberstone, T., Ebrahimjee, F., Thomas, J. M., Churchill, G. C., et al. (2020). Patient fibroblast circadian rhythms predict lithium sensitivity in bipolar disorder. Mol. Psychiatry doi: 10.1038/s41380-020-0769-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Schibler, U., Gotic, I., Saini, C., Gos, P., Curie, T., Emmenegger, Y., et al. (2015). Clock-talk: interactions between central and peripheral circadian oscillators in mammals. Cold Spring Harb. Symp. Quant. Biol. 80, 223–232. doi: 10.1101/sqb.2015.80.027490

PubMed Abstract | CrossRef Full Text | Google Scholar

Schmutz, I., Chavan, R., Ripperger, J. A., Maywood, E. S., Langwieser, N., Jurik, A., et al. (2014). A specific role for the REV-ERBalpha-controlled L-type voltage-gated calcium channel CaV1.2 in resetting the circadian clock in the late night. J. Biol. Rhythms 29, 288–298. doi: 10.1177/0748730414540453

PubMed Abstract | CrossRef Full Text | Google Scholar

Selcho, M., Millan, C., Palacios-Munoz, A., Ruf, F., Ubillo, L., Chen, J., et al. (2017). Central and peripheral clocks are coupled by a neuropeptide pathway in Drosophila. Nat. Commun. 8:15563.

Google Scholar

Shi, L., Ko, M. L., and Ko, G. Y. (2009). Rhythmic expression of microRNA-26a regulates the L-type voltage-gated calcium channel alpha1C subunit in chicken cone photoreceptors. J. Biol. Chem. 284, 25791–25803. doi: 10.1074/jbc.m109.033993

PubMed Abstract | CrossRef Full Text | Google Scholar

Smith, W., Rybczynski, R., and Gilbert, L. (2012). Insect Endocrinology. New York, NY: Academic Press.

Google Scholar

Stadler, F., Schmutz, I., Schwaller, B., and Albrecht, U. (2010). Lack of calbindin-D28k alters response of the murine circadian clock to light. Chronobiol. Int. 27, 68–82. doi: 10.3109/07420521003648554

PubMed Abstract | CrossRef Full Text | Google Scholar

Striessnig, J., Ortner, N. J., and Pinggera, A. (2015). Pharmacology of L-type calcium channels: novel drugs for old targets? Curr. Mol. Pharmacol. 8, 110–122. doi: 10.2174/1874467208666150507105845

PubMed Abstract | CrossRef Full Text | Google Scholar

Takahashi, J. S. (2017). Transcriptional architecture of the mammalian circadian clock. Nat. Rev. Genet. 18, 164–179. doi: 10.1038/nrg.2016.150

PubMed Abstract | CrossRef Full Text | Google Scholar

Tanenhaus, A. K., Zhang, J., and Yin, J. C. (2012). In vivo circadian oscillation of dCREB2 and NF-kappaB activity in the Drosophila nervous system. PLoS One 7:e45130. doi: 10.1371/journal.pone.0045130

PubMed Abstract | CrossRef Full Text | Google Scholar

Tedesco, D., and Haragsim, L. (2012). Cyclosporine: a review. J. Transplant. 2012:230386.

Google Scholar

Videnovic, A., Lazar, A. S., Barker, R. A., and Overeem, S. (2014). ‘The clocks that time us’–circadian rhythms in neurodegenerative disorders. Nat. Rev. Neurol. 10, 683–693. doi: 10.1038/nrneurol.2014.206

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Q., Abruzzi, K. C., Rosbash, M., and Rio, D. C. (2018). Striking circadian neuron diversity and cycling of Drosophila alternative splicing. Elife 7:e35618.

Google Scholar

Welsh, D. K., Takahashi, J. S., and Kay, S. A. (2010). Suprachiasmatic nucleus: cell autonomy and network properties. Annu. Rev. Physiol. 72, 551–577. doi: 10.1146/annurev-physiol-021909-135919

PubMed Abstract | CrossRef Full Text | Google Scholar

White, W. B., Anders, R. J., Macintyre, J. M., Black, H. R., and Sica, D. A. (1995). Nocturnal dosing of a novel delivery system of verapamil for systemic hypertension. Verapamil Study Group. Am. J. Cardiol. 76, 375–380. doi: 10.1016/s0002-9149(99)80104-0

CrossRef Full Text | Google Scholar

Yamanaka, N., Marques, G., and O’connor, M. B. (2015). Vesicle-mediated steroid hormone secretion in Drosophila melanogaster. Cell 163, 907–919. doi: 10.1016/j.cell.2015.10.022

PubMed Abstract | CrossRef Full Text | Google Scholar

Yokota, S., Yamamoto, M., Moriya, T., Akiyama, M., Fukunaga, K., Miyamoto, E., et al. (2001). Involvement of calcium-calmodulin protein kinase but not mitogen-activated protein kinase in light-induced phase delays and Per gene expression in the suprachiasmatic nucleus of the hamster. J. Neurochem. 77, 618–627. doi: 10.1046/j.1471-4159.2001.00270.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, R., Lahens, N. F., Ballance, H. I., Hughes, M. E., and Hogenesch, J. B. (2014). A circadian gene expression atlas in mammals: implications for biology and medicine. Proc. Natl. Acad. Sci. U.S.A. 111, 16219–16224. doi: 10.1073/pnas.1408886111

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, X., Odom, D. T., Koo, S. H., Conkright, M. D., Canettieri, G., Best, J., et al. (2005). Genome-wide analysis of cAMP-response element binding protein occupancy, phosphorylation, and target gene activation in human tissues. Proc. Natl. Acad. Sci. U.S.A. 102, 4459–4464. doi: 10.1073/pnas.0501076102

PubMed Abstract | CrossRef Full Text | Google Scholar