UCD School of Medicine, University College Dublin, UCD Conway Institute, Belfield, Dublin 4, Ireland.
Irish Centre for Vascular Biology, Royal College of Surgeons in Ireland, 123 St. Stephen's Green 123, Dublin 2, Ireland.
Biosci Rep. 2024 May 29;44(5). doi: 10.1042/BSR20231420.
Platelets are small anucleate blood cells supporting vascular function. They circulate in a quiescent state monitoring the vasculature for injuries. Platelets adhere to injury sites and can be rapidly activated to secrete granules and to form platelet/platelet aggregates. These responses are controlled by signalling networks that include G proteins and their regulatory guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs). Recent proteomics studies have revealed the complete spectrum of G proteins, GEFs, and GAPs present in platelets. Some of these proteins are specific for platelets and very few have been characterised in detail. GEFs and GAPs play a major role in setting local levels of active GTP-bound G proteins in response to activating and inhibitory signals encountered by platelets. Thus, GEFs and GAPs are highly regulated themselves and appear to integrate G protein regulation with other cellular processes. This review focuses on GAPs of small G proteins of the Arf, Rab, Ras, and Rho families, as well as of heterotrimeric G proteins found in platelets.
血小板是支持血管功能的小型无核血细胞。它们处于静止状态循环,监测血管损伤。血小板黏附在损伤部位,并可迅速被激活以分泌颗粒并形成血小板/血小板聚集物。这些反应由信号网络控制,包括 G 蛋白及其调节鸟嘌呤核苷酸交换因子 (GEF) 和 GTPase 激活蛋白 (GAP)。最近的蛋白质组学研究揭示了血小板中存在的完整 G 蛋白、GEF 和 GAP 谱。其中一些蛋白质是血小板特有的,很少有详细描述。GEF 和 GAP 在响应血小板遇到的激活和抑制信号时,在设定活性 GTP 结合 G 蛋白的局部水平方面发挥主要作用。因此,GEF 和 GAP 本身受到高度调节,并且似乎将 G 蛋白调节与其他细胞过程集成在一起。本文综述了血小板中发现的 Arf、Rab、Ras 和 Rho 家族的小 G 蛋白以及异三聚体 G 蛋白的 GAP。