Schlossmann Jens, Desch Matthias
Institut für Pharmakologie und Toxikologie, Universität Regensburg, Regensburg, 93055, Germany.
Handb Exp Pharmacol. 2009(191):163-93. doi: 10.1007/978-3-540-68964-5_9.
Signalling of cGK (cGMP-dependent protein kinases) are mediated through phosphorylation of specific substrates. Several substrates of cGKI and cGKII were identified meanwhile. Some cGKI substrates are specifically regulated by the cGKIalpha or the cGKIbeta isozyme. In various cells and tissues, different cGK substrates exist that are essential for the regulation of diverse functions comprising tissue contractility, cell motility, cell contact, cellular secretion, cell proliferation, and cell differentiation. On the molecular level, cGKI substrates fulfill various cellular functions regulating e.g. the intracellular calcium and potassium concentration, the calcium sensitivity, and the organisation of the intracellular cytoskeleton. cGKII substrates are involved e.g. in chloride transport, sodium/proton transport and transcriptional regulation. The understanding of cGK signalling and function depends strongly on the identification of further specific substrates. In the last years, diverse approaches ranging from biochemistry to genetic deletion lead to the identification and establishment of several substrates, which raised new insights in the molecular mechanisms of cGK functions and elucidated new cellular cGK functions. However, the analysis of the dynamic signalling of cGK in tissues and cells will be necessary to discover new signalling pathways and substrates.
cGK(环鸟苷酸依赖性蛋白激酶)的信号传导是通过特定底物的磷酸化介导的。同时鉴定出了几种cGKI和cGKII的底物。一些cGKI底物受到cGKIα或cGKIβ同工酶的特异性调节。在各种细胞和组织中,存在不同的cGK底物,它们对于调节包括组织收缩性、细胞运动性、细胞接触、细胞分泌、细胞增殖和细胞分化在内的多种功能至关重要。在分子水平上,cGKI底物发挥着各种细胞功能,例如调节细胞内钙和钾的浓度、钙敏感性以及细胞内细胞骨架的组织。cGKII底物例如参与氯离子转运、钠/质子转运和转录调控。对cGK信号传导和功能的理解在很大程度上依赖于进一步鉴定特定底物。在过去几年中,从生物化学到基因敲除等多种方法导致了几种底物的鉴定和确立,这为cGK功能的分子机制带来了新的见解,并阐明了新的细胞cGK功能。然而,分析cGK在组织和细胞中的动态信号传导对于发现新的信号通路和底物是必要的。