Patton Andrew P, Smyllie Nicola J, Chesham Johanna E, Hastings Michael H
MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom.
MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, United Kingdom
J Neurosci. 2022 Jul 13;42(28):5522-5537. doi: 10.1523/JNEUROSCI.2337-21.2022.
The suprachiasmatic nucleus (SCN) is the master circadian clock of mammals, generating and transmitting an internal representation of environmental time that is produced by the cell-autonomous transcriptional/post-translational feedback loops (TTFLs) of the 10,000 neurons and 3500 glial cells. Recently, we showed that TTFL function in SCN astrocytes alone is sufficient to drive circadian timekeeping and behavior, raising questions about the respective contributions of astrocytes and neurons within the SCN circuit. We compared their relative roles in circadian timekeeping in mouse SCN explants, of either sex. Treatment with the glial-specific toxin fluorocitrate revealed a requirement for metabolically competent astrocytes for circuit-level timekeeping. Recombinase-mediated genetically complemented Cryptochrome (Cry) proteins in Cry1-deficient and/or Cry2-deficient SCNs were used to compare the influence of the TTFLs of neurons or astrocytes in the initiation of oscillation or in pacemaking. While neurons and astrocytes both initiated oscillation and lengthened the period equally, their kinetics were different, with astrocytes taking twice as long. Furthermore, astrocytes could shorten the period, but not as potently as neurons. Chemogenetic manipulation of Gi- and Gq-coupled signaling pathways in neurons acutely advanced or delayed the ensemble phase, respectively. In contrast, comparable manipulations in astrocytes were without effect. Thus, astrocytes can initiate SCN rhythms and bidirectionally control the SCN period, albeit with lower potency than neurons. Nevertheless, their activation does not influence the SCN phase. The emergent SCN properties of high-amplitude oscillation, initiation of rhythmicity, pacemaking, and phase are differentially regulated: astrocytes and neurons sustain the ongoing oscillation, but its phase is determined by neurons. The hypothalamic suprachiasmatic nucleus (SCN) encodes and disseminates time-of-day information to allow mammals to adapt their physiology to daily environmental cycles. Recent investigations have revealed a role for astrocytes, in addition to neurons, in the regulation of this rhythm. Using pharmacology, genetic complementation, and chemogenetics, we compared the abilities of neurons and astrocytes in determining the emergent SCN properties of high-amplitude oscillation, initiation of rhythmicity, pacemaking, and determination of phase. These findings parameterize the circadian properties of the astrocyte population in the SCN and reveal the types of circadian information that astrocytes and neurons can contribute within their heterogeneous cellular network.
视交叉上核(SCN)是哺乳动物的主生物钟,它产生并传递环境时间的内部表征,这一表征由10000个神经元和3500个神经胶质细胞的细胞自主转录/翻译后反馈环(TTFLs)产生。最近,我们发现仅SCN星形胶质细胞中的TTFL功能就足以驱动昼夜节律计时和行为,这引发了关于SCN回路中星形胶质细胞和神经元各自贡献的问题。我们比较了它们在雌雄小鼠SCN外植体昼夜节律计时中的相对作用。用神经胶质特异性毒素氟代柠檬酸处理表明,对于回路水平的计时,需要代谢功能正常的星形胶质细胞。在Cry1缺陷和/或Cry2缺陷的SCN中,利用重组酶介导的基因互补隐花色素(Cry)蛋白来比较神经元或星形胶质细胞的TTFLs在振荡起始或起搏中的影响。虽然神经元和星形胶质细胞都能启动振荡并同等程度地延长周期,但它们的动力学不同,星形胶质细胞所需时间是神经元的两倍。此外,星形胶质细胞可以缩短周期,但效果不如神经元显著。对神经元中Gi和Gq偶联信号通路进行化学遗传学操作,分别使整体相位急性提前或延迟。相比之下,对星形胶质细胞进行类似操作则没有效果。因此,星形胶质细胞可以启动SCN节律并双向控制SCN周期,尽管效力低于神经元。然而,它们的激活并不影响SCN相位。SCN的高振幅振荡、节律性起始、起搏和相位等新兴特性受到不同调节:星形胶质细胞和神经元维持正在进行的振荡,但其相位由神经元决定。下丘脑视交叉上核(SCN)编码并传播一天中的时间信息,使哺乳动物能够使其生理机能适应每日的环境周期。最近的研究表明,除了神经元外,星形胶质细胞在这种节律的调节中也发挥作用。我们使用药理学、基因互补和化学遗传学方法,比较了神经元和星形胶质细胞在决定SCN的高振幅振荡、节律性起始、起搏和相位等新兴特性方面的能力。这些发现确定了SCN中星形胶质细胞群体的昼夜节律特性,并揭示了星形胶质细胞和神经元在其异质细胞网络中可以贡献的昼夜节律信息类型。