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血管活性肠肽通过 ERK1/2 和 DUSP4 信号控制视交叉上核生物钟网络。

Vasoactive intestinal peptide controls the suprachiasmatic circadian clock network via ERK1/2 and DUSP4 signalling.

机构信息

MRC Laboratory of Molecular Biology, Francis Crick Ave, Cambridge, CB2 0QH, UK.

Department of Neurosurgery, Stanford University, 318 Campus Drive, Stanford, CA, 94305, USA.

出版信息

Nat Commun. 2019 Feb 1;10(1):542. doi: 10.1038/s41467-019-08427-3.

Abstract

The suprachiasmatic nucleus (SCN) co-ordinates circadian behaviour and physiology in mammals. Its cell-autonomous circadian oscillations pivot around a well characterised transcriptional/translational feedback loop (TTFL), whilst the SCN circuit as a whole is synchronised to solar time by its retinorecipient cells that express and release vasoactive intestinal peptide (VIP). The cell-autonomous and circuit-level mechanisms whereby VIP synchronises the SCN are poorly understood. We show that SCN slices in organotypic culture demonstrate rapid and sustained circuit-level circadian responses to VIP that are mediated at a cell-autonomous level. This is accompanied by changes across a broad transcriptional network and by significant VIP-directed plasticity in the internal phasing of the cell-autonomous TTFL. Signalling via ERK1/2 and tuning by its negative regulator DUSP4 are critical elements of the VIP-directed circadian re-programming. In summary, we provide detailed mechanistic insight into VIP signal transduction in the SCN at the level of genes, cells and neural circuit.

摘要

视交叉上核 (SCN) 协调哺乳动物的昼夜行为和生理学。其细胞自主的昼夜节律振荡围绕着一个特征明显的转录/翻译反馈环 (TTFL) 旋转,而整个 SCN 回路通过表达和释放血管活性肠肽 (VIP) 的视网膜接收细胞与太阳时间同步。VIP 使 SCN 同步的细胞自主和回路水平机制尚不清楚。我们表明,器官型培养中的 SCN 切片对 VIP 表现出快速而持续的回路水平昼夜反应,这种反应是在细胞自主水平上介导的。这伴随着广泛的转录网络变化,并伴随着细胞自主 TTFL 的内部相位的显著 VIP 导向可塑性。ERK1/2 信号转导及其负调节剂 DUSP4 的调节是 VIP 定向昼夜重编程的关键因素。总之,我们提供了 SCN 中 VIP 信号转导在基因、细胞和神经回路水平的详细机制见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00b3/6358603/971fe9465d68/41467_2019_8427_Fig1_HTML.jpg

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