Department of Biochemistry, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, the Netherlands.
J Thromb Haemost. 2013 Jan;11(1):2-16. doi: 10.1111/jth.12045.
Platelets in a thrombus interact with (anti)coagulation factors and support blood coagulation. In the concept of cell-based control of coagulation, three different roles of platelets can be distinguished: control of thrombin generation, support of fibrin formation, and regulation of fibrin clot retraction. Here, we postulate that different populations of platelets with distinct surface properties are involved in these coagulant functions. Platelets with elevated Ca(2+) and exposed phosphatidylserine control thrombin and fibrin generation, while platelets with activated α(IIb) β(3) regulate clot retraction. We review how coagulation factor binding depends on the platelet activation state. Furthermore, we discuss the ligands, platelet receptors and downstream intracellular signaling pathways implicated in these coagulant functions. These insights lead to an adapted model of platelet-based coagulation.
血小板在血栓中与(抗)凝血因子相互作用,并支持血液凝固。在基于细胞的凝血控制概念中,可以区分血小板的三个不同作用:控制凝血酶生成、支持纤维蛋白形成和调节纤维蛋白凝块回缩。在这里,我们假设不同表面特性的血小板群体参与这些凝血功能。具有升高的 Ca(2+)和暴露的磷脂酰丝氨酸的血小板控制凝血酶和纤维蛋白生成,而具有激活的 α(IIb)β(3)的血小板调节凝块回缩。我们回顾了凝血因子结合如何取决于血小板的激活状态。此外,我们还讨论了涉及这些凝血功能的配体、血小板受体和下游细胞内信号通路。这些见解导致了基于血小板的凝血的改进模型。