Dr Christilla Bachelot-Loza, INSERM UMR_S U765, Université Paris Descartes, Faculté de Pharmacie, 4 avenue de l'Observatoire, 75006 Paris, France, Tel : +33 153739619, E-mail:
Thromb Haemost. 2013 Dec;110(6):1215-22. doi: 10.1160/TH13-04-0335. Epub 2013 Aug 22.
Clot retraction is an essential step during primary haemostasis, thereby promoting thrombus stability and wound healing. Integrin αIIbβ3 plays a critical role in clot retraction, by inducing acto-myosin interactions that allow platelet cytoskeleton reorganisation. However, the signalling pathways that lead to clot retraction are still misunderstood. In this study, we report the first data on the kinetics of myosin II light chain (MLC) phosphorylation during clot retraction. We found an early phosphorylation peak followed by a second peak. By using specific inhibitors of kinases and small G proteins, we showed that MLC kinase (MLCK), RhoA/ROCK, and Rac-1 were involved in clot retraction and in the early MLC phosphorylation peak. Only Rac-1 and actin polymerisation, controlled by outside-in signalling, were crucial to the second MLC phosphorylation peak.
血栓收缩是初级止血过程中的一个重要步骤,可促进血栓稳定性和伤口愈合。整合素 αIIbβ3 通过诱导肌动球蛋白相互作用,允许血小板细胞骨架重新组织,在血栓收缩中起关键作用。然而,导致血栓收缩的信号通路仍不明确。在这项研究中,我们报告了在血栓收缩过程中肌球蛋白 II 轻链 (MLC) 磷酸化动力学的首批数据。我们发现了一个早期磷酸化峰,随后是第二个峰。通过使用激酶和小 G 蛋白的特异性抑制剂,我们表明肌球蛋白轻链激酶 (MLCK)、RhoA/ROCK 和 Rac-1 参与了血栓收缩和早期 MLC 磷酸化峰。只有 Rac-1 和由外向内信号控制的肌动蛋白聚合对于第二个 MLC 磷酸化峰至关重要。