Diverse roles of pontine NPS-expressing neurons in sleep regulation

Author:

Xing Lijuan1,Zou Xianlin1,Yin Chen1,Webb John M.1,Shi Guangsen2,Ptáček Louis J.1345,Fu Ying-Hui1345

Affiliation:

1. Department of Neurology, University of California San Francisco, San Francisco, CA 94143

2. Zhongshan Institute for Drug Discovery, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Zhongshan 528400, China

3. Department of Neurology, Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA 94143

4. Kavli Institute for Fundamental Neuroscience, University of California San Francisco, San Francisco, CA 94143

5. Institute of Human Genetics, University of California San Francisco, San Francisco, CA 94143

Abstract

Neuropeptide S (NPS) was postulated to be a wake-promoting neuropeptide with unknown mechanism, and a mutation in its receptor (NPSR1) causes the short sleep duration trait in humans. We investigated the role of different NPS + nuclei in sleep/wake regulation. Loss-of-function and chemogenetic studies revealed that NPS + neurons in the parabrachial nucleus (PB) are wake-promoting, whereas peri-locus coeruleus (peri-LC) NPS + neurons are not important for sleep/wake modulation. Further, we found that a NPS + nucleus in the central gray of the pons (CGPn) strongly promotes sleep. Fiber photometry recordings showed that NPS + neurons are wake-active in the CGPn and wake/REM-sleep active in the PB and peri-LC. Blocking NPS–NPSR1 signaling or knockdown of Nps supported the function of the NPS–NPSR1 pathway in sleep/wake regulation. Together, these results reveal that NPS and NPS + neurons play dichotomous roles in sleep/wake regulation at both the molecular and circuit levels.

Funder

NIH

Publisher

Proceedings of the National Academy of Sciences

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