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      Neurochemical Heterogeneity Among Lateral Hypothalamic Hypocretin/Orexin and Melanin-Concentrating Hormone Neurons Identified Through Single-Cell Gene Expression Analysis

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          Abstract

          The lateral hypothalamic area (LHA) lies at the intersection of multiple neural and humoral systems and orchestrates fundamental aspects of behavior. Two neuronal cell types found in the LHA are defined by their expression of hypocretin/orexin (Hcrt/Ox) and melanin-concentrating hormone (MCH) and are both important regulators of arousal, feeding, and metabolism. Conflicting evidence suggests that these cell populations have a more complex signaling repertoire than previously appreciated, particularly in regard to their coexpression of other neuropeptides and the machinery for the synthesis and release of GABA and glutamate. Here, we undertook a single-cell expression profiling approach to decipher the neurochemical phenotype, and heterogeneity therein, of Hcrt/Ox and MCH neurons. In transgenic mouse lines, we used single-cell quantitative polymerase chain reaction (qPCR) to quantify the expression of 48 key genes, which include neuropeptides, fast neurotransmitter components, and other key markers, which revealed unexpected neurochemical diversity. We found that single MCH and Hcrt/Ox neurons express transcripts for multiple neuropeptides and markers of both excitatory and inhibitory fast neurotransmission. Virtually all MCH and approximately half of the Hcrt/Ox neurons sampled express both the machinery for glutamate release and GABA synthesis in the absence of a vesicular GABA release pathway. Furthermore, we found that this profile is characteristic of a subpopulation of LHA glutamatergic neurons but contrasts with a broad population of LHA GABAergic neurons. Identifying the neurochemical diversity of Hcrt/Ox and MCH neurons will further our understanding of how these populations modulate postsynaptic excitability through multiple signaling mechanisms and coordinate diverse behavioral outputs.

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Nature, nurture, or chance: stochastic gene expression and its consequences.

            Gene expression is a fundamentally stochastic process, with randomness in transcription and translation leading to cell-to-cell variations in mRNA and protein levels. This variation appears in organisms ranging from microbes to metazoans, and its characteristics depend both on the biophysical parameters governing gene expression and on gene network structure. Stochastic gene expression has important consequences for cellular function, being beneficial in some contexts and harmful in others. These situations include the stress response, metabolism, development, the cell cycle, circadian rhythms, and aging.
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              Neural substrates of awakening probed with optogenetic control of hypocretin neurons.

              The neural underpinnings of sleep involve interactions between sleep-promoting areas such as the anterior hypothalamus, and arousal systems located in the posterior hypothalamus, the basal forebrain and the brainstem. Hypocretin (Hcrt, also known as orexin)-producing neurons in the lateral hypothalamus are important for arousal stability, and loss of Hcrt function has been linked to narcolepsy. However, it is unknown whether electrical activity arising from Hcrt neurons is sufficient to drive awakening from sleep states or is simply correlated with it. Here we directly probed the impact of Hcrt neuron activity on sleep state transitions with in vivo neural photostimulation, genetically targeting channelrhodopsin-2 to Hcrt cells and using an optical fibre to deliver light deep in the brain, directly into the lateral hypothalamus, of freely moving mice. We found that direct, selective, optogenetic photostimulation of Hcrt neurons increased the probability of transition to wakefulness from either slow wave sleep or rapid eye movement sleep. Notably, photostimulation using 5-30 Hz light pulse trains reduced latency to wakefulness, whereas 1 Hz trains did not. This study establishes a causal relationship between frequency-dependent activity of a genetically defined neural cell type and a specific mammalian behaviour central to clinical conditions and neurobehavioural physiology.
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                Author and article information

                Journal
                eNeuro
                eNeuro
                eneuro
                eneuro
                eNeuro
                eNeuro
                Society for Neuroscience
                2373-2822
                1 September 2017
                22 September 2017
                Sep-Oct 2017
                : 4
                : 5
                : ENEURO.0013-17.2017
                Affiliations
                [1 ]Department of Physiology and Neurobiology, University of Connecticut , Storrs, CT 06269
                [2 ]Department of Molecular and Cell Biology, University of Connecticut , Storrs, CT 06269
                [3 ]Department of Biomedical Engineering, University of Connecticut , Storrs, CT 06269
                [4 ]Department of Statistics, University of Connecticut , Storrs, CT 06269
                [5 ]Connecticut Institute for the Brain and Cognitive Sciences, University of Connecticut , Storrs, CT 06269
                Author notes

                The authors declare no competing financial interests.

                Author contributions: L.E.M, F.W.K., C.E.N. and A.C.J. designed research; L.E.M., F.W.K., B.R.C., A.F., C.N. and A.C.J. performed research; L.E.M, F.W.K., B.R.C., A.F., K.C. and A.C.J. analyzed data; L.E.M., F.W.K. and A.C.J. wrote the paper.

                This work was supported by a K99/R00 (R00MH097792) and an R01 (R01MH112739) from the National Institute of Mental Health (to A.C.J.) and the National Institutes of Health Shared Instrumentation Grant S10OD016435 (PI: Dr. Akiko Nishiyama) for imaging support.

                [*]

                L.E.M. and F.W.K. contributed equally to this work.

                Correspondence should be addressed to Alexander C. Jackson. Dept. Physiology and Neurobiology, University of Connecticut, Storrs, CT 06269. E-mail: alexander.jackson@ 123456uconn.edu .
                Author information
                http://orcid.org/0000-0001-7489-3946
                Article
                eN-NWR-0013-17
                10.1523/ENEURO.0013-17.2017
                5617207
                28966976
                18ab6e66-1f5f-4c80-b3d3-bfdc49a1d22a
                Copyright © 2017 Mickelsen et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 11 January 2017
                : 14 August 2017
                : 25 August 2017
                Page count
                Figures: 9, Tables: 2, Equations: 0, References: 133, Pages: 24, Words: 17729
                Funding
                Funded by: http://doi.org/10.13039/100000025 HHS | NIH | National Institute of Mental Health (NIMH)
                Award ID: R00MH097792
                Award ID: R01MH112739
                Categories
                5
                5.1
                New Research
                Integrative Systems
                Custom metadata
                September/October 2017

                cotransmission,hypocretin/orexin,lateral hypothalamic area,melanin-concentrating hormone,neuropeptide,neurotransmitter

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