Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.
Thromb Haemost. 2009 Dec;102(6):1149-56. doi: 10.1160/TH09-05-0289.
Vascular injury leads to formation of a structured thrombus as a consequence of platelet activation and aggregation, thrombin and fibrin formation, and trapping of leukocytes and red cells. This review summarises current evidence for heterogeneity of platelet responses and functions in the thrombus-forming process. Environmental factors contribute to response heterogeneity, as the platelets in a thrombus adhere to different substrates, and sense specific (ant)agonists and rheological conditions. Contraction of platelets and interaction with fibrin and other blood cells cause further response variation. On the other hand, response heterogeneity can also be due to intrinsic differences between platelets in age and in receptor and signalling proteins. As a result, at least three subpopulations of platelets are formed in a thrombus: aggregating platelets with (reversible) integrin activation, procoagulant (coated) platelets exposing phosphatidylserine and binding coagulation factors, and contracting platelets with cell-cell contacts. This recognition of thrombus heterogeneity has implications for the use and development of antiplatelet medication.
血管损伤会导致血小板激活和聚集、凝血酶和纤维蛋白形成以及白细胞和红细胞的捕获,从而形成结构有序的血栓。本综述总结了目前关于血栓形成过程中血小板反应和功能异质性的证据。环境因素促成了反应的异质性,因为血栓中的血小板黏附在不同的基质上,并感知特定的(抗)激动剂和流变学条件。血小板的收缩以及与纤维蛋白和其他血细胞的相互作用导致了进一步的反应变化。另一方面,反应的异质性也可能是由于血小板在年龄、受体和信号蛋白方面存在内在差异。因此,在血栓中至少形成了三种血小板亚群:具有(可逆)整合素激活的聚集血小板、暴露磷脂酰丝氨酸并结合凝血因子的促凝(包被)血小板以及具有细胞-细胞接触的收缩血小板。这种对血栓异质性的认识对抗血小板药物的使用和开发具有重要意义。