Hoffman M, Monroe D M, Oliver J A, Roberts H R
Department of Pathology, Durham Veterans Affairs Medical Center, Durham, NC 27705, USA.
Blood. 1995 Sep 1;86(5):1794-801.
Tissue factor is the major initiator of coagulation. Both factor IX and factor X are activated by the complex of factor VIIa and tissue factor (VIIa/TF). The goal of this study was to determine the specific roles of factors IXa and Xa in initiating coagulation. We used a model system of in vitro coagulation initiated by VIIa/TF and that included unactivated platelets and plasma concentrations of factors II, V, VIII, IX, and X, tissue factor pathway inhibitor, and antithrombin III. In some cases, factor IX and/or factor X were activated by tissue factor-bearing monocytes, but in some experiments, picomolar concentrations of preactivated factor IX or factor X were used to initiate the reactions. Timed samples were assayed for both platelet activation and thrombin activity. Factor Xa was 10 times more potent than factor IXa in initiating platelet activation, but factor IXa was much more effective in promoting thrombin generation than was factor Xa. In the presence of VIIa/TF, factor X was required for both platelet activation and thrombin generation, while factor IX was only required for thrombin generation. We conclude that VIIa/TF-activated factors IXa and Xa have distinct physiologic roles. The main role of factor Xa that is initially activated by VIIa/TF is to activate platelets by generating an initial, small amount of thrombin in the vicinity of platelets. Factor IXa, on the other hand, enhances thrombin generation by providing factor Xa on the platelet surface, leading to prothrombinase formation. Only tiny amounts of factors IX and X need to be activated by VIIa/TF to perform these distinct functions. Our experiments show that initiation of coagulation is highly dependent on activation of small amounts of factors IXa and Xa in proximity to platelet surfaces and that these factors play distinct roles in subsequent events, leading to an explosion of thrombin generation. Furthermore, the specific roles of factors IXa and Xa generated by VIIa/TF are not necessarily reflected by the kinetics of factor IXa and Xa generation.
组织因子是凝血的主要启动因子。因子IX和因子X均由因子VIIa与组织因子(VIIa/TF)的复合物激活。本研究的目的是确定因子IXa和Xa在启动凝血过程中的具体作用。我们使用了由VIIa/TF启动的体外凝血模型系统,该系统包括未活化的血小板以及因子II、V、VIII、IX和X的血浆浓度、组织因子途径抑制物和抗凝血酶III。在某些情况下,因子IX和/或因子X由携带组织因子的单核细胞激活,但在一些实验中,使用皮摩尔浓度的预活化因子IX或因子X来启动反应。定时采集样本检测血小板活化和凝血酶活性。在启动血小板活化方面,因子Xa的效力比因子IXa高10倍,但在促进凝血酶生成方面,因子IXa比因子Xa有效得多。在VIIa/TF存在的情况下,血小板活化和凝血酶生成均需要因子X,而凝血酶生成仅需要因子IX。我们得出结论,VIIa/TF激活的因子IXa和Xa具有不同的生理作用。最初由VIIa/TF激活的因子Xa的主要作用是通过在血小板附近生成少量初始凝血酶来激活血小板。另一方面,因子IXa通过在血小板表面提供因子Xa来增强凝血酶生成,从而导致凝血酶原酶形成。VIIa/TF仅需激活极少量的因子IX和X即可执行这些不同的功能。我们的实验表明,凝血的启动高度依赖于血小板表面附近少量因子IXa和Xa的激活,并且这些因子在随后的事件中发挥不同的作用,导致凝血酶生成的爆发。此外,VIIa/TF产生的因子IXa和Xa的特定作用不一定反映在因子IXa和Xa生成的动力学上。