Isomura Akihiro, Kageyama Ryoichiro
Institute for Frontier Life and Medical Sciences, Kyoto University; Japan Science and Technology Agency, PRESTO;
Institute for Frontier Life and Medical Sciences, Kyoto University; Institute for Integrated Cell-Material Sciences, Kyoto University; Graduate School of Medicine, Kyoto University; Graduate School of Biostudies, Kyoto University;
J Vis Exp. 2018 Mar 22(133):57149. doi: 10.3791/57149.
Cells should respond properly to temporally changing environments, which are influenced by various factors from surrounding cells. The Notch signaling pathway is one of such essential molecular machinery for cell-to-cell communications, which plays key roles in normal development of embryos. This pathway involves a cell-to-cell transfer of oscillatory information with ultradian rhythms, but despite the progress in molecular biology techniques, it has been challenging to elucidate the impact of multicellular interactions on oscillatory gene dynamics. Here, we present a protocol that permits optogenetic control and live monitoring of gene expression patterns in a precise temporal manner. This method successfully revealed that intracellular and intercellular periodic inputs of Notch signaling entrain intrinsic oscillations by frequency tuning and phase shifting at the single-cell resolution. This approach is applicable to the analysis of the dynamic features of various signaling pathways, providing a unique platform to test a functional significance of dynamic gene expression programs in multicellular systems.
细胞应能对随时间变化的环境做出适当反应,这种环境受周围细胞各种因素的影响。Notch信号通路是细胞间通讯的重要分子机制之一,在胚胎正常发育中起关键作用。该通路涉及具有超日节律的振荡信息的细胞间传递,但尽管分子生物学技术取得了进展,阐明多细胞相互作用对振荡基因动态的影响仍然具有挑战性。在此,我们提出了一种方案,该方案允许以精确的时间方式对基因表达模式进行光遗传学控制和实时监测。该方法成功揭示,Notch信号的细胞内和细胞间周期性输入通过在单细胞分辨率下的频率调谐和相移来带动固有振荡。这种方法适用于分析各种信号通路的动态特征,为测试多细胞系统中动态基因表达程序的功能意义提供了一个独特的平台。