Differential arousal regulation by prokineticin 2 signaling in the nocturnal mouse and the diurnal monkey. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Zhou, Qun-Yong; Burton, Katherine; Neal, Matthew; Qiao, Yu; Kanthasamy, Anumantha; Sun, Yanjun; Xu, Xiangmin; Ma, Yuanye; Li, Xiaohan
• Is Part Of: Molecular brain. Volume 9:Issue 1(2016)
• Page Start: 1
• Page End: 11
• Publication Date: 2016-12
• Subjects: Circadian clock output -- Wakefulness -- Sleep -- Diurnal -- Nocturnal -- Prokineticin 2 -- Oscillation -- Intrinsically photosensitive retinal ganglion cells -- Suprachiasmatic nucleus -- Superior colliculus; Brain -- Periodicals; Molecular biology -- Periodicals; 573.86
• DOI: 10.1186/s13041-016-0255-x
• Languages: English
• ISSNs: 1756-6606

Abstract

Abstract 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.