Deletion of Clock Gene Period1 (Per1) in Neurons but Not in Astrocytes Shortens Clock Period and Diminishes Light-Mediated Rapid Phase Advances in Mice.

IF 3.2 Q3 CLINICAL NEUROLOGY
Dan-Adrian Epuran, Urs Albrecht
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Abstract

The circadian clock enables organisms to anticipate daily recurring events and synchronize their internal rhythms with environmental cues, such as light, aligning with the day/night cycle. Central to the molecular mechanisms of the circadian clock and light sensing are the Period (Per) 1 and 2 genes. While the roles of Per2 in astrocytes and neurons have been characterized, the specific contributions of Per1 remain less understood. Previous research has shown that Per2 in neurons, but not astrocytes, influences phase shifts, whereas the regulation of the circadian period involves Per2 in both cell types. In this study, we investigated the role of Per1 in neurons and astrocytes in modulating the circadian period and phase shifts. Using an Aschoff Type I protocol (constant darkness) combined with 15 min light pulses at circadian times (CT) 10, 14, and 22, we found that the absence of Per1 in neurons-but not in astrocytes-significantly affected both the circadian period and phase advance shifts in response to light at CT22.

在小鼠神经元中删除时钟基因周期1 (Per1),而在星形胶质细胞中不删除,可缩短时钟周期并减少光介导的快速相位推进。
生物钟使生物体能够预测每天重复发生的事件,并使其内部节律与环境线索(如光线)同步,与昼夜周期保持一致。昼夜节律钟和光感应的分子机制的中心是周期(Per) 1和2基因。虽然Per2在星形胶质细胞和神经元中的作用已经被表征,但Per1的具体贡献仍然知之甚少。先前的研究表明,神经元中的Per2影响相移,而星形胶质细胞中没有,而昼夜节律周期的调节涉及两种细胞类型的Per2。在这项研究中,我们研究了Per1在神经元和星形胶质细胞中调节昼夜节律和相移的作用。使用Aschoff I型方案(持续黑暗)结合在昼夜节律时间(CT) 10,14和22的15分钟光脉冲,我们发现神经元中Per1的缺失-而不是星形胶质细胞-显着影响了昼夜节律周期和在CT22时响应光的相移。
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来源期刊
Clocks & Sleep
Clocks & Sleep Multiple-
CiteScore
4.40
自引率
0.00%
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审稿时长
7 weeks
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