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Gq-Ca2+ 轴控制视交叉上核中 circadian time 的电路水平编码。

A Gq-Ca2+ axis controls circuit-level encoding of circadian time in the suprachiasmatic nucleus.

机构信息

Division of Neurobiology, Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.

出版信息

Neuron. 2013 May 22;78(4):714-28. doi: 10.1016/j.neuron.2013.03.011. Epub 2013 Apr 25.

Abstract

The role of intracellular transcriptional/post-translational feedback loops (TTFL) within the circadian pacemaker of the suprachiasmatic nucleus (SCN) is well established. In contrast, contributions from G-coupled pathways and cytosolic rhythms to the intercellular control of SCN pacemaking are poorly understood. We therefore combined viral transduction of SCN slices with fluorescence/bioluminescence imaging to visualize GCaMP3-reported circadian oscillations of intracellular calcium [Ca2+]i alongside activation of Ca2+ /cAMP-responsive elements. We phase-mapped them to the TTFL, in time and SCN space, and demonstrated their dependence upon G-coupled vasoactive intestinal peptide (VIP) signaling. Pharmacogenetic manipulation revealed the individual contributions of Gq, Gs, and Gi to cytosolic and TTFL circadian rhythms. Importantly, activation of Gq-dependent (but not Gs or Gi) pathways in a minority of neurons reprogrammed [Ca2+]i and TTFL rhythms across the entire SCN. This reprogramming was mediated by intrinsic VIPergic signaling, thus revealing a Gq/[Ca2+]i-VIP leitmotif and unanticipated plasticity within network encoding of SCN circadian time.

摘要

细胞内转录/翻译后反馈环(TTFL)在视交叉上核(SCN)的生物钟中的作用已得到充分证实。相比之下,G 蛋白偶联途径和细胞质节律对 SCN 起搏的细胞间控制的贡献还知之甚少。因此,我们将 SCN 切片的病毒转导与荧光/生物发光成像相结合,以可视化 GCaMP3 报告的细胞内钙 [Ca2+]i 的昼夜节律波动,以及 Ca2+ / cAMP 反应元件的激活。我们将它们与时相映射到 TTFL,并在时间和 SCN 空间上进行了演示,证明它们依赖于 G 蛋白偶联的血管活性肠肽(VIP)信号。药理遗传操作揭示了 Gq、Gs 和 Gi 对细胞质和 TTFL 昼夜节律的单独贡献。重要的是,少数神经元中 Gq 依赖性(而非 Gs 或 Gi 依赖性)途径的激活可在整个 SCN 中重新编程 [Ca2+]i 和 TTFL 节律。这种重编程是由内在的 VIP 能信号介导的,从而揭示了 SCN 昼夜节律编码中的 Gq/[Ca2+]i-VIP 主导主题和意想不到的可塑性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2370/3666084/3d64c79dfb79/gr1.jpg

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