Department of Biochemistry, University of Vermont College of Medicine, Burlington, Vt 05405, USA.
Arterioscler Thromb Vasc Biol. 2010 Dec;30(12):2400-7. doi: 10.1161/ATVBAHA.110.216531. Epub 2010 Nov 11.
The goal of this study was to define and characterize the subpopulation of platelets capable of regulating the functional interactions of factors Va (FVa) and Xa (FXa) on the thrombin-activated platelet surface.
Flow cytometric analyses were used to define and characterize platelet subpopulations. At a concentration of thrombin known to elicit maximal platelet activation, platelet-derived FVa release, and prothrombinase assembly/function, only a subpopulation of platelets was positive for FVa and FXa binding. An additional subpopulation bound lower levels of FVa but little, if any, FXa. Fluorescence microscopy analyses confirmed these data. Phenotypically, platelets capable of binding FXa were more highly reticulated and demonstrated significantly increased expression of several key adhesion molecules, including P-selectin, glycoprotein Ibα, and integrins α(IIb) and β(3). This platelet subpopulation was also defined by the expression of a nondissociable, membrane-bound pool of functional platelet-derived FVa, which made up ≈35% to 50% of the total membrane-bound cofactor.
The ability of activated platelets to support thrombin generation is defined by a subpopulation of platelets expressing a nondissociable pool of platelet-derived FVa and increased adhesive receptor density. This subpopulation is hypothesized to play a significant role in regulating both normal hemostasis and pathological thrombus formation because the adherent properties of platelets and their ability to mount and sustain a procoagulant response are crucial steps in both of these processes.
本研究旨在定义和描述能够调节凝血酶激活血小板表面因子 Va(FVa)和 Xa(FXa)功能相互作用的血小板亚群。
采用流式细胞术分析来定义和描述血小板亚群。在已知能够引起血小板最大激活、血小板源性 FVa 释放和凝血酶原酶组装/功能的凝血酶浓度下,只有一小部分血小板对 FVa 和 FXa 结合呈阳性。另一亚群结合的 FVa 水平较低,但结合的 FXa 很少或没有。荧光显微镜分析证实了这些数据。表型上,能够结合 FXa 的血小板具有更高的网织化程度,并表现出几种关键黏附分子(包括 P-选择素、糖蛋白 Ibα 和整合素 α(IIb)和β(3))的表达显著增加。该血小板亚群还通过表达不可分离的、膜结合的功能性血小板源性 FVa 池来定义,该池约占总膜结合辅因子的 35%至 50%。
激活血小板支持凝血酶生成的能力由表达不可分离的血小板源性 FVa 池和增加的黏附受体密度的血小板亚群定义。假设该亚群在调节正常止血和病理性血栓形成中发挥重要作用,因为血小板的黏附特性及其引发和维持促凝反应的能力是这两个过程中的关键步骤。