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Constant light enhances synchrony among circadian clock cells and promotes behavioral rhythms in VPAC2-signaling deficient mice

机译:恒定光增强生物钟细胞之间的同步性并促进VpaC2信号传导缺陷小鼠的行为节律

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摘要

Individual neurons in the suprachiasmatic nuclei (SCN) contain an intracellular molecular clock and use intercellular signaling to synchronize their timekeeping activities so that the SCN can coordinate brain physiology and behavior. The neuropeptide vasoactive intestinal polypeptide (VIP) and its VPAC2 receptor form a key component of intercellular signaling systems in the SCN and critically control cellular coupling. Targeted mutations in either the intracellular clock or intercellular neuropeptide signaling mechanisms, such as VIP-VPAC2 signaling, can lead to desynchronization of SCN neuronal clocks and loss of behavioral rhythms. An important goal in chronobiology is to develop interventions to correct deficiencies in circadian timekeeping. Here we show that extended exposure to constant light promotes synchrony among SCN clock cells and the expression of ~24 h rhythms in behavior in mice in which intercellular signaling is disrupted through loss of VIP-VPAC2 signaling. This study highlights the importance of SCN synchrony for the expression of rhythms in behavior and reveals how non-invasive manipulations in the external environment can be used to overcome neurochemical communication deficits in this important brain system.
机译:视交叉上核(SCN)中的单个神经元包含一个细胞内分子时钟,并使用细胞间信号来同步其计时活动,从而使SCN可以协调大脑的生理和行为。神经肽血管活性肠多肽(VIP)及其VPAC2受体形成SCN中细胞间信号系统的关键组成部分,并严格控制细胞偶联。细胞内时钟或细胞间神经肽信号转导机制(例如VIP-VPAC2信号转导)中的靶向突变可能导致SCN神经元时钟失步并丧失行为节律。时间生物学的一个重要目标是开发干预措施,以纠正昼夜节律的不足。在这里,我们显示长时间暴露在恒定光下会促进SCN时钟细胞之间的同步性,并在行为中的〜24 h节律的表达在小鼠中,其中细胞间信号通过VIP-VPAC2信号的丢失而被破坏。这项研究强调了SCN同步对于行为节律表达的重要性,并揭示了如何在外部环境中使用非侵入性操作来克服这一重要大脑系统中的神经化学通讯缺陷。

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