Department of Pharmacology and Molecular Sciences, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Nat Chem Biol. 2011 Jan;7(1):34-40. doi: 10.1038/nchembio.478. Epub 2010 Nov 21.
Many protein kinases are key nodal signaling molecules that regulate a wide range of cellular functions. These functions may require complex spatiotemporal regulation of kinase activities. Here, we show that protein kinase A (PKA), Ca(2+) and cyclic AMP (cAMP) oscillate in sync in insulin-secreting MIN6 beta cells, forming a highly integrated oscillatory circuit. We found that PKA activity was essential for this oscillatory circuit and was capable of not only initiating the signaling oscillations but also modulating their frequency, thereby diversifying the spatiotemporal control of downstream signaling. Our findings suggest that exquisite temporal control of kinase activity, mediated via signaling circuits resulting from cross-regulation of signaling pathways, can encode diverse inputs into temporal parameters such as oscillation frequency, which in turn contribute to proper regulation of complex cellular functions in a context-dependent manner.
许多蛋白激酶是关键的节点信号分子,调节广泛的细胞功能。这些功能可能需要激酶活性的复杂时空调节。在这里,我们表明,蛋白激酶 A(PKA)、Ca2+和环 AMP(cAMP)在胰岛素分泌的 MIN6β细胞中同步振荡,形成一个高度整合的振荡电路。我们发现 PKA 活性对于这个振荡电路是必不可少的,它不仅能够启动信号振荡,还能够调节它们的频率,从而多样化下游信号的时空控制。我们的发现表明,通过信号通路的交叉调节产生的信号电路对激酶活性的精确时间控制,可以将不同的输入编码为时间参数,如振荡频率,从而有助于以依赖于上下文的方式对复杂的细胞功能进行适当的调节。