Heterogeneity of hypocretin/orexin neurons

Executive summary

The multi-functional, hypothalamic hypocretin/orexin (HCRT) producing neurons regulate an array of physiological and behavioral states including arousal, sleep, feeding, emotions, stress, and reward. How a presumably uniform HCRT neuron population regulates such a diverse set of functions is not clear. The role of the HCRT neuropeptides may vary depending on the timing and localization of secretion and neuronal activity. Moreover, HCRT neuropeptides may not mediate all functions ascribed to HCRT neurons. Some could be orchestrated by additional neurotransmitters and neuropeptides that are expressed in HCRT neurons. We hypothesize that HCRT neurons are segregated into genetically-, anatomically- and functionally-distinct subpopulations. We discuss accumulating data that suggest the existence of such HCRT neuron subpopulations that may effectuate the diverse functions of these neurons in mammals and fish.

Introduction

The hypothalamus region in the brain regulates diverse physiological and behavioral processes such as arousal, sleep, feeding, reproduction and autonomic control, by integrating external and internal stimuli [1]. Among the millions of neurons in the hypothalamus, a group of only a few thousand hypocretin/orexin (HCRT) producing neurons stands out as a key regulator of sleep and wakefulness. HCRT neurons secrete the HCRT1 and HCRT2 neuropeptides and are located in the lateral hypothalamus area (LHA) and the adjacent perifornical area (PeFLH) [2,3]. In mice, approximately 5,000 HCRT neurons project to wide areas in the brain, including the tuberomammillary nucleus (TMN), paraventricular thalamic nucleus, arcuate nucleus, and monoaminergic nuclei, which express the two G-protein coupled receptors HCRTR1 and HCRTR2 [4–6]. In accordance with the broad anatomical projections, the function of HCRT neurons includes primarily the regulation of the sleep/wake cycle, but also that of feeding, energy homeostasis, emotion, stress response, motivation, and reward.

Now, how could one type of neuron defined through the expression of HCRT peptides serve as a multi-functional hypothalamic system supporting such diverse physiological processes? The secretion of HCRT neuropeptides at different effector sites in the brain could, for instance, be differentially regulated. The differential and spatially restricted release of HCRT1 and HCRT2, and the different signaling through differentially expressed HCRTR1 and HCRTR2 could be another determining factor. In addition, HCRT neurons also contain other neurotransmitters and proteins that may be involved in regulating their development, plasticity and diverse functions.

Soon after the discovery of the two HCRT neuropeptides [2,3], it was found that loss of HCRT signaling, either by loss of the ligand or receptor, results in the sleep disorder narcolepsy in humans, and causes narcolepsy-like symptoms in animals [7–9]. Narcolepsy is characterized by fragmented sleep and wakefulness during day and night, and a signature symptom; cataplexy – a sudden skeletal muscle atonia during wakefulness, which is triggered by emotional stimuli [10]. Several discoveries have linked the HCRT system to narcolepsy, including the isolation of mutated HCRTR2 in narcoleptic dogs [7], the narcolepsy-like phenotype of HCRT knockout mice [2,8], the detection of low HCRT protein levels in narcoleptic patients [9], and the severe loss of HCRT neurons in the brains of narcoleptic patients [11–13]. This tight association between the HCRT system, narcolepsy, and sleep disturbances established the HCRT system as a key regulator of arousal and sleep/wake transitions.

The HCRT system is unique to vertebrates, although recent work has characterized a functional HCRT neuropeptide in the basal chordate, amphioxus [14]. Since 2004, the HCRT system has been studied in the simple vertebrate, zebrafish [15,16]. This diurnal animal emerged as a popular model to study neurodevelopment and behavior, including the hypothalamic regulation of sleep [17]. The zebrafish has a simple, but conserved, brain anatomy and function with mammals [18]. In addition, it is amenable for genetic manipulation, using transposase- [19] and clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein 9 (Cas9)- based genome editing [20]. Unlike most other vertebrates, the brain of the larva zebrafish is transparent, making it suitable for time-lapse imaging of single cells and organelles [21,22], optogenetics, and brain-wide imaging of genetically encoded calcium markers [23,24]. Furthermore, the zebrafish is well suited for large-scale genetic-, pharmacological-, and behavioral-screens [25,26]. Zebrafish sleep was defined using behavioral criteria, specifically through reduction of voluntary movement during the night, clock-controlled rhythmic activity that peaks during the day, reversibility, specific posture, increased arousal thresholds, and sleep rebound post-sleep deprivation [27–32]. Two major sleep signatures have been characterized in zebrafish; slow bursting sleep and propagating wave sleep, which share commonalities with mammalian slow-wave sleep and paradoxical or rapid-eye-movement (REM) sleep, respectively [33].

The zebrafish HCRT neuronal network is simple: comprised of about 20 neurons in larvae and about 60 neurons in adults (Table 1) [16,27,31,34]. The zebrafish HCRT system includes a single hcrt gene, which encodes both HCRT1 and HCRT2 peptides [34], and only one HCRT receptor, which is structurally more similar to the mammalian HCRTR2. Similar to mammals, zebrafish HCRT neurons are located in the LHA and project to the telencephalon, diencephalon, mesencephalon, rhombencephalon, and the pineal gland, toward the noradrenergic, dopaminergic, serotonergic, cholinergic, histaminergic and melatonergic nuclei [15,16,21,27,31,34–36]. Overexpression of HCRT in the entire body of larval zebrafish induces wakefulness [27], and both the HCRT neuron-ablated larvae and the HCRT-receptor mutant (Hcrtr^−/−) adult zebrafish exhibit sleep fragmentation, as is observed in narcoleptic patients [29,31]. Overall, the relative simplicity of the HCRT system in zebrafish makes this vertebrate an ideal model to study the diverse functions of HCRT neuronal networks.

Table 1.

The HCRT system in zebrafish, rodents, and humans

	Zebrafish	Rodents	Humans
Number of HCRT neurons	~20–60	~5,000	~70,000 [12]
Type of peptides	HCRT1 and HCRT2	HCRT1 and HCRT2	HCRT1 and HCRT2 [2]
Type of receptors	HCRTR2	HCRTR1 and HCRTR2	HCRTR1 and HCRTR2 [2]
Brain regions	LHA	LHA, DMH and PeFLH	LHA and PHA [93]
Main functions studied	Sleep and wakefulness, feeding	Sleep and wakefulness, feeding, energy homeostasis, emotions, stress response, and reward	Sleep and wakefulness, feeding, emotions, social interaction, and reward [94,95]

DMH, dorsomedial hypothalamus; HCRT, hypocretin; HCRTR, hypocretin receptor; LHA, lateral hypothalamic area; PeFLH, perifornical part of lateral hypothalamus area; PHA, posterior hypothalamic area.

It is generally assumed that HCRT neurons are a relatively homogeneous population; however, finer granularity may exist. In this chapter, we discuss the hypothesis that HCRT neurons can control multiple functions due to their heterogeneous genetics, anatomy, and functionality. We raise the possibility of functional HCRT subpopulations with distinct gene expression, activity, and connectivity profiles.

The genetic profile of HCRT neurons

The molecular marker that defines the HCRT neurons is the HCRT neuropeptide. However, these neurons contain other distinct proteins, which are expressed in small to large subsets of HCRT neurons, in addition to other regions of the brain. In order to study the comprehensive molecular identity of HCRT neurons, several studies have been conducted in human, rodents, and fish. They have revealed an array of genes that are expressed in subpopulations of HCRT neurons or in almost all of the cells, suggesting molecular heterogeneity (Table 2).

Table 2.

Specific gene and protein expression signatures that define HCRT neuron populations in rodents

Proteins and mRNAs expressed in most HCRT neurons		Proteins and mRNAs expressed in a subset of HCRT neurons
PDYN	Chou et al., 2001 [37]	IGFBP3	Honda et al., 2009 [47]
NARP/NPTX2*	Reti et al., 2002 [38]	TRIB2	Cvetkovic-Lopes et al., 2010 [48]
CCKAR	Tsujino et al., 2005 [42]	PCSK1, NGB, DLK1, GPX3, LGALS3, LHX9*	Dalal et al., 2013 [50]
ENTPD3/NTPDase3*	Belcher et al., 2006 [46]	CART, PENK	Mickelsen et al., 2017 [40]
NNAT, CELF6, STAT5B, RFX4*	Dalal et al., 2013 [50]	PEG3, TLR2, ARHGAP36, IRS4	Seifinejad et al., 2019 [55]
NUCB2	Mickelsen et al., 2017 [40]	QRFP	Takahashi et al., 2020 [53]

Only mRNAs/proteins that were anatomically verified are listed. Proteins/mRNAs that are expressed in HCRT neurons of both zebrafish and rodents are marked with *.

ARHGAP36, Rho GTPase-activating protein 36; CART, cocaine and amphetamine regulatory transcript; CCK_AR, cholecystokinin A receptor; CELF6, CUGBP elav-like family member 6; DLK1, delta like non-canonical notch ligand 1; ENTPD3/NTPDase3, ectonucleoside triphosphate diphosphohydrolase 3; GPX3, glutathione peroxidase 3; IGFBP3, insulin-like growth factor-binding protein 3; IRS4, insulin receptor substrate 4; LGALS3, galectin 3; LHX9, LIM homeobox 9; NARP/NPTX2, neuronal pentraxin 2; NGB, neuroglobin; NNAT, neuronatin; NUCB2, nucleobindin 2; PCSK1, proprotein convertase subtilisin/kexin type 1; PDYN, prodynorphin; PEG3, paternally-expressed gene 3; PENK, proenkephalin; QRFP, pyroglutamylated RFamide peptide; RFX4, regulatory factor X4; STAT5B, signal transducer and activator of transcription 5B; TLR2, toll-like receptor 2; TRIB2, tribbles homolog 2.

Among the mRNA and/or proteins expressed in almost all HCRT neurons are the secreted proteins, prodynorphin (PDYN) and neuronal activity-regulated pentraxin II (NARP/NPTX2). These two proteins have been used to show that the cells, and not only the HCRT ligand, are absent in narcoleptic patients [11,37–39]. In human brains, at least 80% of the HCRT-producing neurons also contain Pdyn mRNA and NARP protein [11]. In the rat hypothalamus, all (>99%) HCRT-positive neurons are NARP-positive [38] and nearly all (94 ± 2%) are PDYN-positive [37]. These two proteins are also expressed widely in additional brain areas, and not restricted to the LHA. Confirming these results, studies in mice have also shown co-expression of Hcrt and Pdyn mRNA in 98.4% of the HCRT neurons using in situ hybridization (ISH) [40]. NARP can enhance postsynaptic responses to glutamate, while PDYN inhibits neuron activity via the κ-opioid receptor [37,41]. However, the role of NARP and PDYN in the HCRT system is undetermined.

Another protein found in almost all HCRT neurons in mice is the cholecystokinin receptor (CCK_AR) [42]. CCK suppresses food intake [43] and locomotor activity [44]. Moreover, studies in rats have reported on co-localization of ectonucleoside triphosphate diphosphohydrolase 3 (ENTPD3/NTPDase3) and the ATP ligand-gated cation channel receptor P2X₂R in almost all HCRT neurons [45,46]. The co-localization of P2X₂R and ENTPD3 in mammalian HCRT neurons suggests that purinergic signaling might modulate the functions of the HCRT system, such as the regulation of sleep and energy metabolism.

The expression of these genetic markers in essentially the whole HCRT neuronal population suggests, at first sight, that these neurons would be homogenous. However, other genes are only expressed in a portion of HCRT neurons. For example, comparison of the transcriptome of narcoleptic versus control postmortem human brains, and transgenic mice lacking HCRT neurons versus wildtype mice, revealed that insulin-like growth factor-binding protein 3 (IGFBP3) colocalizes in ~80% of HCRT neurons in mice but only in 10–20% of HCRT neurons in humans [47]. It was suggested that elevated IGFBP3 levels in HCRT cells could decrease HCRT production and wakefulness under physiological conditions. Another protein expressed only in a subset of HCRT neurons is tribbles homolog 2 (TRIB2), an intracellular protein produced by HCRT neurons and other cell types that is targeted by antibodies in a fraction of patients with narcolepsy [48,49]. TRIB2-specific antibody-containing serum of a narcoleptic patient showed that 87% of HCRT neurons in the mouse hypothalamus are co-stained by the serum [48].

Using the translating ribosome affinity purification assay, 188 transcripts were identified as robustly enriched in HCRT neurons [50], including the known HCRT cell markers Pdyn, Narp, and Igfbp3. Moreover, few novel genes and gene products had substantial overlap with HCRT neurons, including CUGBP elav-like family member 6 (CELF6), neuronatin (NNAT), signal transducer and activator of transcription 5b (STAT5b) and regulatory factor x4 (RFX4), with the latter expressed only within these neurons. In contrast, several gene products were expressed only in a subset of HCRT neurons, revealing molecular heterogeneity in these neurons: proprotein convertase subtilisin/kexin type 1 (PCSK1, 42 ± 4.6 % co-localization), neuroglobin (NGB, 54 ± 3.6 %), glutathione peroxidase 3 (GPX3, 29 ± 9.3 %), galectin 3 (LGALS3, 35 ± 5.8 %), delta like non-canonical notch ligand 1 (DLK1, 44 ± 10 %) and LIM homeobox 9 mRNA (Lhx9, 76 ± 3.6 % co-localization) [50]. Ablation of Lhx9 resulted in more than 30% loss of HCRT neurons, without a general disruption of hypothalamic development. It appears that Lhx9 can regulate the development and specification of a subset, but not of all, HCRT neurons [50]. It remains to be determined whether these genetic variations reflect the transient expression state of the neurons at a given state or rather represent functionally-distinct subsets of HCRT populations.

Single-cell RNA-sequencing (scRNA-seq) of the mouse hypothalamus found partial co-localization of pyroglutamylated RFamide peptide (Qrfp) and Hcrt mRNA [51]. QRFP is a hypothalamic peptide that has been implicated in food intake, activity, anxiety, cardiovascular functions, arousal and hibernation-like state [52–54]. QRFP is lost together with HCRT neurons in Hcrt-ablated mice [55]. However, IHC and transgenesis showed that QRFP and HCRT do not colocalize in the same hypothalamic neurons in zebrafish and mice [54,56]. This can be explained by the differences in sensitivity of the sequencing and histological techniques. Surprisingly, recent IHC assay in mice showed that few QRFP-positive neurons also express HCRT [53]. Altogether, these experiments suggest that a low number of HCRT neurons co-express QRFP, which may help mediate the function of a small subpopulation of HCRT neurons.

RNA-sequencing of purified HCRT neurons and comparison to other hypothalamic cells revealed an array of differentially expressed genes in mice. This work used IHC to show that paternally-expressed gene 3 (PEG3), toll-like receptor 2 (TLR2), rho GTPase-activating protein 36 (ARHGAP36) and insulin receptor substrate 4 (IRS4) partially colocalize with HCRT [55]. Moreover, loss of Peg3 in mice significantly reduced HCRT cell numbers, while knock-down of a Peg3 in zebrafish completely abolished Hcrt expression, resulting in a two-fold increase in the amount of sleep [55].

The development of single-cell gene expression analysis enables through-profiling of the genetic identity of distinct neurons. This method was used to show in mice that the most extensively co-expressed transcripts in HCRT neurons are Pdyn (100% co-localization), Lhx9 (100%), Igfbp3 (100%), Nptx2/Narp (100%), Celf6 (100%), and Nnat (98%), which were discussed above. This method also revealed new candidate genes, such as nucleobindin 2 (Nucb2, 100%), proenkephalin (Penk, 76.8%), and cocaine and amphetamine regulatory prepropeptide (Cartpt, 42.0%) [40]. Validation of the results using ISH and IHC showed that although Nucb2 mRNA (84.4%) and NUCB2 protein (99.2%) colocalize with the majority of HCRT neurons, Penk (31.4%) and Cartpt (8.4%) positive cells had limited overlap with HCRT neurons, and immunoreactive CART protein was barely detected in HCRT neurons (0.8%) [40]. This last observation suggests that few HCRT neurons contain Cartpt mRNA but only a small amount of detectable protein.

These extensive studies have resulted in a list of genes that are expressed in many or in a few of HCRT neurons (Table 2). However, the complexity of the mammalian brain, which includes thousands of dense HCRT neurons that are intermingled with other hypothalamic neurons, have raised experimental challenges to isolate and study an uncontaminated HCRT neuronal population. In contrast, the relatively simple brain of the zebrafish enables the identification of specific HCRT neurons. The Hcrt promoter and transgenic tg(Hcrt:EGFP) zebrafish [35] provides an optimal model to profile the genetic identity of HCRT neurons. In zebrafish, similar to the findings in mammals, the Entpd3 and the P2X receptor P2rx8, which mediate purinergic signaling, are expressed in a small subset of HCRT neurons in larvae. These findings suggest that HCRT neurons mediate purinergic signaling by cell surface P2X receptors and Entpd3, which control the extracellular concentration and accessibility of ATP [57]. As adenosine signaling has been linked to sleep regulation in zebrafish [58], these results suggest that some HCRT neurons regulate metabolism and the sleep/wake cycle by sensing purine nucleotides. An additional gene found to be expressed in a subset of HCRT neurons in the zebrafish lateral hypothalamus (LH) is Nptx2b [21]. Moreover, a study of the leptin-neurotensin (Nts)-HCRT neuronal circuit demonstrated that a portion of both larvae and adult HCRT neurons express the Nts receptor [59], suggesting that Nts neurons regulate the function of HCRT neurons in zebrafish, as in mammals [60].

We isolated and sequenced the entire HCRT neuronal population using fluorescence-activated cell sorting (FACS) and whole transcriptome RNA-sequencing in zebrafish larvae. Hundreds of novel HCRT-neuron-specific transcripts were identified [61]. The functional roles of the genes were diverse and included regulation of metabolism, sleep, synaptogenesis, and synaptic plasticity. A comparison between the HCRT-neuron-specific candidate genes isolated in zebrafish [61] and mice [50] showed that at least eight genes (Rfx4, Lhx9, Scg2, Vgll2, Ptprn, Creb3l1, Sgsm1, and Fam46a) are found in HCRT neurons in both vertebrates. Verification of the results using double-staining showed that while several genes, including Kcnh4a, Hmx3, Lhx9 and Dennd1b, were expressed in most HCRT neurons, the majority, including Star, Fam46a, and Zgc171844 were expressed only in a subset of HCRT neurons. Notably, the portion of co-localization with HCRT in larvae was similar to that in adults. Intriguingly, similar to the finding in mice, Lhx9 can induce the specification of HCRT neurons in zebrafish [50,61,62].

Altogether, the studies in mammals and zebrafish suggest that the functional diversity of HCRT neurons can be regulated by their diverse molecular actors. Considering that the HCRT neuropeptides are only two of the secreted players, and additional proteins and neurotransmitters are likely to play a role in the function of the neurons, we suggest that the HCRT neurons do not necessarily act as one homogenous unit, but rather are divided into functionally-distinct subpopulations. Understanding the function of the genes that are differentially expressed in HCRT subpopulations will provide the basis to elucidate the mechanism that regulates the multi-functions of HCRT neurons.

The various HCRT interactions with other neuronal populations

Another approach to classify the heterogeneity of HRCT neurons is by connectivity of their upstream and downstream projections. Previous studies have examined HCRT neuronal afferent and efferent projections using traditional and genetically targeted neuroanatomical tracing methods in rodents. In general, HCRT neurons integrate a wide variety of neural signals from multiple sources distributed all over the brain, including the TMN, paraventricular thalamic nucleus, arcuate nucleus, cholinergic and monoaminergic nuclei [4–6,63–65]. Additionally, HCRT-expressing neurons are excited by a wide variety of neurotransmitters, including glutamate [66], ATP [67], corticotropin releasing factor [68], thyrotropin releasing hormone [69], noradrenaline [70], and acetylcholine [66,70], and they are inhibited by GABA [66] and adenosine [71,72]. In turn, HCRT neurons project diffusely throughout the brain, with especially dense excitatory projections to brain areas regulating arousal (e.g. locus coeruleus [LC] and TMN), reward (e.g. ventral tegmental area [VTA] and nucleus accumbens [NAc]) and autonomic function (e.g. brainstem sympathetic and respiratory control centers). An open question remains as to whether there are distinct HCRT cell clusters that exhibit different afferent and efferent projection maps?

To systematically determine the afferents to the HCRT neurons, researchers used retrograde and anterograde tracing to identify direct inputs to HCRT neurons in rat. They found that anterograde tracers injected into the brainstem and reward-related nuclei preferentially mark the lateral part of the HCRT field, while injections into the ventromedial hypothalamus (VMH) and other hypothalamic regions preferentially stain HCRT neurons in the medial and PeFLH field [65].

Output projections from HCRT neurons also demonstrate a preference between brain regions. A number of studies have shown that HCRT neurons can be anatomically subdivided into at least two separate subpopulations: one subpopulation is thought to reside in the medial HCRT field in the PeFLH and dorsomedial hypothalamus (DMH), sending projections to the LC and TMN, while the other subpopulation is thought to reside in the lateral HCRT field in the LHA, sending projections to the VTA and NAc (Figure 1) [73–77]. Moreover, only a portion of HCRT neurons project to the sublaterodorsal tegmental nucleus (SLD) and regulate the activation of REM sleep [78]. In contrast, a study in mice suggests that although HCRT neurons can be classified based on their downstream projections, these classifications do not show a lateral/medial topographic location within the hypothalamus. Based on retrograde tracing of target neurons, HCRT neurons that project to both the LC and TMN or to both the VTA and NAc were identified, however, these subpopulations were intermingled [79].

Fig. 1. Possible functional heterogeneity of HCRT neurons.

Schematic illustration of proposed functional heterogeneity of HCRT neurons. The unique transcriptional profile, neuronal activity, and synaptic processing and connectivity of HCRT neurons suggest that the multi-functional HCRT neurons can be divided into distinct functional subpopulations in all vertebrates.

In agreement with findings in rodents, in zebrafish, HCRT neurons have been shown to innervate and functionally interact with noradrenergic neurons [80] and the histaminergic system [81] in the LC and TMN, respectively. Further study in mammals and comparison to simpler vertebrates can shed light on the projection variabilities within the HCRT neuronal populations. Segregated HCRT neuronal projections may interact with their targets selectively. Whether these anatomically distinct HCRT populations display autonomous activity patterns, physiological and behavioral characteristics, require further investigation.

The diverse functions of HCRT neurons

Considering the heterogeneity of gene expression and neuronal connectivity, the diverse functions of HCRT neurons in regulating various behaviors such as feeding, sleep, stress, motivation and reward, might indeed be regulated by different subpopulations. Accumulating data suggest that HCRT neurons are divided into distinct functional subpopulations because of variability in intrinsic electrical and synaptic properties [82], or because of differential regulation by drugs and behavioral paradigms [74]. In this section, we discuss data that suggest that HCRT neurons are functionally diverse.

At the cellular level, HCRT neurons can be functionally subdivided into two populations based on their electrophysiological properties. Unbiased statistical analysis of electrical properties of HCRT neurons in combination with 3-D analysis of their shape, pointed to an existence of two subgroups of HCRT neurons in the mouse brain that have unique ‘electrical fingerprints’ and distinct ways of receiving information from other neurons [82]. Moreover, electrophysiological and calcium imaging data have demonstrated a wide array of neuronal activity patterns in HCRT neurons, although retrograde tracers injected into either the LC or VTA do not seem to preferentially label specific active classes of HCRT neurons [83].

It has been proposed that HCRT neurons in the LH regulate motivation and reward, whereas HCRT neurons located in the PeFLH and DMH regulate arousal and response to stress (Figure 1) [73]. For example, during wakefulness, the expression of the neuronal activity marker Fos is increased in PeFLH HCRT neurons, but not in the lateral HCRT neurons [84]. In a rodent model of depression, HCRT neurons located in the PeFLH and DMH regions are found to be more sensitive to unpredictable chronic mild stress than HCRT neurons located in the LH [85]. In contrast, the reward of food or drug induces activity in the lateral HCRT neurons [74]. Studies have shown that morphine administration increase Fos expression in the lateral HCRT neurons [75] and intermittent access to cocaine activates the lateral HCRT subpopulation, while selective knock-down of lateral HCRT neurons reduces motivation for cocaine [86].

Similar to mammals, the HCRT system in zebrafish consolidates sleep and wakefulness [15], induces food intake [87], and modulates neural circuitry of stress [88]. Neural activity of freely behaving larvae, monitored using Ca²⁺-dependent bioluminescence, was associated with periods of increased locomotor activity [89]. However, functional differences between subclasses of HCRT neurons in zebrafish is unknown and require further research.

Future directions

The HCRT system has been extensively studied in humans and multiple animal models, ranging from zebrafish and cavefish to rodents and primates [15,90–92]. Since their discovery, HCRT neurons have been defined based on their cellular marker – the HCRT neuropeptides – and largely treated as one homogenous population. However, accumulating data suggest functional, anatomical, and genetic heterogeneity of HCRT neurons because of the diverse expression profiles of molecular actors and synaptic connections, as well as cell-specific activity. These findings offer new interpretations for previous studies in the field and may help to understand the role of the HCRT system in health and disease.

Further studies are required in order to decipher and characterize the anatomy and function of subpopulations of HCRT neurons. For example, single-cell RNA-seq experiments can identify and profile genetically defined HCRT neuronal subpopulations. These genetically distinct subpopulations can be functionally characterized using imaging of neural activity markers during the sleep/wake cycle, feeding, stress and reward states. These experiments can be followed by manipulation of HCRT neuronal subpopulations using optogenetics, synaptic silencing, and genetically-induced neuron ablation, in order to understand the unique role of each HCRT neuronal networks.

Key Take-Home Points.

• The hypothalamic hypocretin/orexin (HCRT) system regulates diverse functions, ranging from arousal and feeding to stress and reward.

• Based on their unique gene expression profile, connections, and activity, we propose that the HCRT neurons are divided into distinct functional subpopulations in all vertebrates.

• The relatively simple zebrafish is an attractive model to study the structure and function of subpopulation of HCRT neurons in single neuron resolution.