Institute of Experimental Biomedicine - Chair I, University Hospital and Rudolf Virchow Center, Würzburg, Germany.
Department of Transfusion Medicine, Institute for Immunology and Transfusion Medicine, University Medicine Greifswald, Greifswald, Germany.
Hamostaseologie. 2021 Feb;41(1):14-21. doi: 10.1055/a-1325-0993. Epub 2021 Feb 15.
Platelet activation and aggregation are essential to limit blood loss at sites of vascular injury but may also lead to occlusion of diseased vessels. The platelet cytoskeleton is a critical component for proper hemostatic function. Platelets change their shape after activation and their contractile machinery mediates thrombus stabilization and clot retraction. In vitro studies have shown that platelets, which come into contact with proteins such as fibrinogen, spread and first form filopodia and then lamellipodia, the latter being plate-like protrusions with branched actin filaments. However, the role of platelet lamellipodia in hemostasis and thrombus formation has been unclear until recently. This short review will briefly summarize the recent findings on the contribution of the actin cytoskeleton and lamellipodial structures to platelet function.
血小板的激活和聚集对于限制血管损伤部位的出血至关重要,但也可能导致病变血管的阻塞。血小板细胞骨架是正常止血功能的关键组成部分。血小板在激活后改变形状,其收缩机制介导血栓稳定和血凝块回缩。体外研究表明,与纤维蛋白原等蛋白质接触的血小板会伸展,并首先形成丝状伪足,然后形成片状伪足,后者是带有分支肌动蛋白丝的板状突起。然而,直到最近,血小板片状伪足在止血和血栓形成中的作用仍不清楚。这篇简短的综述将简要总结最近关于肌动蛋白细胞骨架和片状伪足结构对血小板功能贡献的发现。