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Differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey

The temporal organization of activity/rest or sleep/wake rhythms for mammals is regulated by the interaction of light/dark cycle and circadian clocks. The neural and molecular mechanisms that confine the active phase to either day or night period for the diurnal and the nocturnal mammals are unclear...

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Autores principales: Zhou, Qun-Yong, Burton, Katherine J., Neal, Matthew L., Qiao, Yu, Kanthasamy, Anumantha G., Sun, Yanjun, Xu, Xiangmin, Ma, Yuanye, Li, Xiaohan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989352/
https://www.ncbi.nlm.nih.gov/pubmed/27535380
http://dx.doi.org/10.1186/s13041-016-0255-x
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author Zhou, Qun-Yong
Burton, Katherine J.
Neal, Matthew L.
Qiao, Yu
Kanthasamy, Anumantha G.
Sun, Yanjun
Xu, Xiangmin
Ma, Yuanye
Li, Xiaohan
author_facet Zhou, Qun-Yong
Burton, Katherine J.
Neal, Matthew L.
Qiao, Yu
Kanthasamy, Anumantha G.
Sun, Yanjun
Xu, Xiangmin
Ma, Yuanye
Li, Xiaohan
author_sort Zhou, Qun-Yong
collection PubMed
description The temporal organization of activity/rest or sleep/wake rhythms for mammals is regulated by the interaction of light/dark cycle and circadian clocks. The neural and molecular mechanisms that confine the active phase to either day or night period for the diurnal and the nocturnal mammals are unclear. Here we report that prokineticin 2, previously shown as a circadian clock output molecule, is expressed in the intrinsically photosensitive retinal ganglion cells, and the expression of prokineticin 2 in the intrinsically photosensitive retinal ganglion cells is oscillatory in a clock-dependent manner. We further show that the prokineticin 2 signaling is required for the activity and arousal suppression by light in the mouse. Between the nocturnal mouse and the diurnal monkey, a signaling receptor for prokineticin 2 is differentially expressed in the retinorecipient suprachiasmatic nucleus and the superior colliculus, brain projection targets of the intrinsically photosensitive retinal ganglion cells. Blockade with a selective antagonist reveals the respectively inhibitory and stimulatory effect of prokineticin 2 signaling on the arousal levels for the nocturnal mouse and the diurnal monkey. Thus, the mammalian diurnality or nocturnality is likely determined by the differential signaling of prokineticin 2 from the intrinsically photosensitive retinal ganglion cells onto their retinorecipient brain targets.
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spelling pubmed-49893522016-08-19 Differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey Zhou, Qun-Yong Burton, Katherine J. Neal, Matthew L. Qiao, Yu Kanthasamy, Anumantha G. Sun, Yanjun Xu, Xiangmin Ma, Yuanye Li, Xiaohan Mol Brain Research The temporal organization of activity/rest or sleep/wake rhythms for mammals is regulated by the interaction of light/dark cycle and circadian clocks. The neural and molecular mechanisms that confine the active phase to either day or night period for the diurnal and the nocturnal mammals are unclear. Here we report that prokineticin 2, previously shown as a circadian clock output molecule, is expressed in the intrinsically photosensitive retinal ganglion cells, and the expression of prokineticin 2 in the intrinsically photosensitive retinal ganglion cells is oscillatory in a clock-dependent manner. We further show that the prokineticin 2 signaling is required for the activity and arousal suppression by light in the mouse. Between the nocturnal mouse and the diurnal monkey, a signaling receptor for prokineticin 2 is differentially expressed in the retinorecipient suprachiasmatic nucleus and the superior colliculus, brain projection targets of the intrinsically photosensitive retinal ganglion cells. Blockade with a selective antagonist reveals the respectively inhibitory and stimulatory effect of prokineticin 2 signaling on the arousal levels for the nocturnal mouse and the diurnal monkey. Thus, the mammalian diurnality or nocturnality is likely determined by the differential signaling of prokineticin 2 from the intrinsically photosensitive retinal ganglion cells onto their retinorecipient brain targets. BioMed Central 2016-08-18 /pmc/articles/PMC4989352/ /pubmed/27535380 http://dx.doi.org/10.1186/s13041-016-0255-x Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhou, Qun-Yong
Burton, Katherine J.
Neal, Matthew L.
Qiao, Yu
Kanthasamy, Anumantha G.
Sun, Yanjun
Xu, Xiangmin
Ma, Yuanye
Li, Xiaohan
Differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey
title Differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey
title_full Differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey
title_fullStr Differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey
title_full_unstemmed Differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey
title_short Differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey
title_sort differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989352/
https://www.ncbi.nlm.nih.gov/pubmed/27535380
http://dx.doi.org/10.1186/s13041-016-0255-x
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