Elvers Margitta
Margitta Elvers, Ph.D., Department of Clinical and Experimental Hemostasis, Hemotherapy and Transfusion Medicine, Heinrich-Heine-University Duesseldorf, Moorenstr. 5, 40225 Duesseldorf, Germany, Tel. +49/(0)211/81-08851, Fax -17498., E-mail:
Hamostaseologie. 2016 Aug 3;36(3):168-77. doi: 10.5482/HAMO-14-09-0046. Epub 2015 Feb 2.
Platelet cytoskeletal reorganization is essential for platelet adhesion and thrombus formation in hemostasis and thrombosis. The Rho GTPases RhoA, Rac1 and Cdc42 are the main players in cytoskeletal dynamics of platelets responsible for the formation of filopodia and lamellipodia to strongly increase the platelet surface upon activation. They are involved in platelet activation and aggregate formation including platelet secretion, integrin activation and arterial thrombus formation. The activity of Rho GTPases is tightly controlled by different proteins such as GTPase-activating proteins (GAPs). GAPs stimulate GTP hydrolysis to terminate Rho signaling. The role and impact of GAPs in platelets is not well-defined and many of the RhoGAPs identified are not known to be present in platelets or to have any function in platelets. The recently identified RhoGAPs Oligophrenin1 (OPHN1) and Nadrin regulate the activity of RhoA, Rac1 and Cdc42 and subsequent platelet cytoskeletal reorganization, platelet activation and thrombus formation. In the last years, the analysis of genetically modified mice helped to gain the understanding of Rho GTPases and their regulators in cytoskeletal rearrangements and other Rho mediated cellular processes in platelets.
血小板细胞骨架重排对于止血和血栓形成过程中的血小板黏附及血栓形成至关重要。Rho GTP酶RhoA、Rac1和Cdc42是血小板细胞骨架动力学的主要参与者,它们负责丝状伪足和片状伪足的形成,从而在激活时显著增加血小板表面积。它们参与血小板激活和聚集体形成,包括血小板分泌、整合素激活及动脉血栓形成。Rho GTP酶的活性受到不同蛋白质(如GTP酶激活蛋白(GAPs))的严格调控。GAPs刺激GTP水解以终止Rho信号传导。GAPs在血小板中的作用和影响尚不明确,许多已鉴定的RhoGAPs在血小板中是否存在或是否具有任何功能也不清楚。最近鉴定出的RhoGAPs少突神经胶质糖蛋白1(OPHN1)和Nadrin可调节RhoA、Rac1和Cdc42的活性以及随后的血小板细胞骨架重排、血小板激活和血栓形成。在过去几年中,对基因敲除小鼠的分析有助于深入了解Rho GTP酶及其调节因子在血小板细胞骨架重排和其他Rho介导的细胞过程中的作用。