Department of Psychiatry and Center for Circadian Biology, University of California, San Diego, La Jolla, CA 92093-0603.
Department of Mathematics and Statistics, Amherst College, Amherst, MA 01002.
eNeuro. 2017 Aug 18;4(4). doi: 10.1523/ENEURO.0160-17.2017. eCollection 2017 Jul-Aug.
Circadian rhythms of mammalian physiology and behavior are coordinated by the suprachiasmatic nucleus (SCN) in the hypothalamus. Within SCN neurons, various aspects of cell physiology exhibit circadian oscillations, including circadian clock gene expression, levels of intracellular Ca ([Ca]), and neuronal firing rate. [Ca] oscillates in SCN neurons even in the absence of neuronal firing. To determine the causal relationship between circadian clock gene expression and [Ca] rhythms in the SCN, as well as the SCN neuronal network dependence of [Ca] rhythms, we introduced GCaMP3, a genetically encoded fluorescent Ca indicator, into SCN neurons from PER2::LUC knock-in reporter mice. Then, PER2 and [Ca] were imaged in SCN dispersed and organotypic slice cultures. In dispersed cells, PER2 and [Ca] both exhibited cell autonomous circadian rhythms, but [Ca] rhythms were typically weaker than PER2 rhythms. This result matches the predictions of a detailed mathematical model in which clock gene rhythms drive [Ca] rhythms. As predicted by the model, PER2 and [Ca] rhythms were both stronger in SCN slices than in dispersed cells and were weakened by blocking neuronal firing in slices but not in dispersed cells. The phase relationship between [Ca] and PER2 rhythms was more variable in cells within slices than in dispersed cells. Both PER2 and [Ca] rhythms were abolished in SCN cells deficient in the essential clock gene . These results suggest that the circadian rhythm of [Ca] in SCN neurons is cell autonomous and dependent on clock gene rhythms, but reinforced and modulated by a synchronized SCN neuronal network.
哺乳动物的生理和行为的昼夜节律由下丘脑的视交叉上核(SCN)协调。在 SCN 神经元中,细胞生理的各个方面都表现出昼夜节律波动,包括昼夜节律钟基因表达、细胞内 Ca([Ca])水平和神经元放电率。即使在没有神经元放电的情况下,SCN 神经元中的 [Ca]也会发生振荡。为了确定 SCN 中昼夜节律钟基因表达与 [Ca]节律之间的因果关系,以及 [Ca]节律对 SCN 神经元网络的依赖性,我们从 PER2::LUC 敲入报告小鼠的 SCN 神经元中引入了 GCaMP3,这是一种遗传编码的荧光 Ca 指示剂。然后,在 SCN 分散和器官型切片培养物中对 PER2 和 [Ca]进行成像。在分散的细胞中,PER2 和 [Ca]都表现出自主的昼夜节律,但 [Ca]节律通常比 PER2 节律弱。这一结果与一个详细的数学模型的预测相匹配,该模型表明时钟基因节律驱动 [Ca]节律。正如该模型所预测的,与分散细胞相比,SCN 切片中的 PER2 和 [Ca]节律都更强,并且在切片中阻断神经元放电会减弱这些节律,但在分散细胞中不会。与 PER2 节律相比,[Ca]节律的相位关系在切片中的细胞中更具可变性。在 SCN 细胞中缺乏必需的时钟基因 时,PER2 和 [Ca]节律都被消除。这些结果表明,SCN 神经元中 [Ca]的昼夜节律是自主的,依赖于时钟基因节律,但由同步的 SCN 神经元网络增强和调节。