MRC Laboratory of Molecular Biology, Francis Crick Ave, Cambridge, CB2 0QH, UK.
Department of Neurosurgery, Stanford University, 318 Campus Drive, Stanford, CA, 94305, USA.
Nat Commun. 2019 Feb 1;10(1):542. doi: 10.1038/s41467-019-08427-3.
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.
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。