Department of Chemical Engineering and the Institute for Applied Life Sciences, University of Massachusetts, Amherst, Massachusetts.
Department of Biology, Washington University in St. Louis, Saint Louis, Missouri.
J Biol Rhythms. 2020 Jun;35(3):287-301. doi: 10.1177/0748730420913672. Epub 2020 Apr 14.
The suprachiasmatic nucleus (SCN) of the hypothalamus consists of a highly heterogeneous neuronal population networked together to allow precise and robust circadian timekeeping in mammals. While the critical importance of SCN neurons in regulating circadian rhythms has been extensively studied, the roles of SCN astrocytes in circadian system function are not well understood. Recent experiments have demonstrated that SCN astrocytes are circadian oscillators with the same functional clock genes as SCN neurons. Astrocytes generate rhythmic outputs that are thought to modulate neuronal activity through pre- and postsynaptic interactions. In this study, we developed an in silico multicellular model of the SCN clock to investigate the impact of astrocytes in modulating neuronal activity and affecting key clock properties such as circadian rhythmicity, period, and synchronization. The model predicted that astrocytes could alter the rhythmic activity of neurons via bidirectional interactions at tripartite synapses. Specifically, astrocyte-regulated extracellular glutamate was predicted to increase neuropeptide signaling from neurons. Consistent with experimental results, we found that astrocytes could increase the circadian period and enhance neural synchronization according to their endogenous circadian period. The impact of astrocytic modulation of circadian rhythm amplitude, period, and synchronization was predicted to be strongest when astrocytes had periods between 0 and 2 h longer than neurons. Increasing the number of neurons coupled to the astrocyte also increased its impact on period modulation and synchrony. These computational results suggest that signals that modulate astrocytic rhythms or signaling (e.g., as a function of season, age, or treatment) could cause disruptions in circadian rhythm or serve as putative therapeutic targets.
视交叉上核(SCN)由一个高度异质的神经元网络组成,共同实现哺乳动物精确而稳健的生物钟。虽然 SCN 神经元在调节生物钟方面的重要性已被广泛研究,但 SCN 星形胶质细胞在生物钟系统功能中的作用尚不清楚。最近的实验表明,SCN 星形胶质细胞是生物钟振荡器,具有与 SCN 神经元相同的功能性时钟基因。星形胶质细胞产生节律性输出,被认为通过突触前和突触后相互作用来调节神经元活动。在这项研究中,我们开发了一个 SCN 时钟的计算机多细胞模型,以研究星形胶质细胞在调节神经元活动和影响关键时钟特性(如昼夜节律性、周期和同步性)方面的作用。该模型预测,星形胶质细胞可以通过三突触的双向相互作用改变神经元的节律性活动。具体来说,星形胶质细胞调节的细胞外谷氨酸被预测会增加神经元的神经肽信号。与实验结果一致,我们发现星形胶质细胞可以根据其内在的生物钟周期,增加神经元的昼夜节律周期并增强神经同步性。当星形胶质细胞的周期比神经元长 0 到 2 小时时,对昼夜节律振幅、周期和同步性的星形胶质细胞调节的影响最大。增加与星形胶质细胞偶联的神经元数量也会增加其对周期调制和同步性的影响。这些计算结果表明,调节星形胶质细胞节律或信号的信号(例如,作为季节、年龄或治疗的函数)可能会导致昼夜节律紊乱或成为潜在的治疗靶点。