Hackeng Tilman M, Seré Kristin M, Tans Guido, Rosing Jan
Department of Biochemistry, Cardiovascular Research Institute Maastricht, University of Maastricht, The Netherlands.
Proc Natl Acad Sci U S A. 2006 Feb 28;103(9):3106-11. doi: 10.1073/pnas.0504240103. Epub 2006 Feb 17.
Tissue factor (TF) plays an important role in hemostasis, inflammation, angiogenesis, and the pathophysiology of atherosclerosis and cancer. In this article we uncover a mechanism in which protein S, which is well known as the cofactor of activated protein C, specifically inhibits TF activity by promoting the interaction between full-length TF pathway inhibitor (TFPI) and factor Xa (FXa). The stimulatory effect of protein S on FXa inhibition by TFPI is caused by a 10-fold reduction of the K(i) of the FXa/TFPI complex, which decreased from 4.4 nM in the absence of protein S to 0.5 nM in the presence of protein S. This decrease in K(i) not only results in an acceleration of the feedback inhibition of the TF-mediated coagulation pathway, but it also brings the TFPI concentration necessary for effective FXa inhibition well within range of the concentration of TFPI in plasma. This mechanism changes the concept of regulation of TF-induced thrombin formation in plasma and demonstrates that protein S and TFPI act in concert in the inhibition of TF activity. Our data suggest that protein S deficiency not only increases the risk of thrombosis by impairing the protein C system but also by reducing the ability of TFPI to down-regulate the extrinsic coagulation pathway.
组织因子(TF)在止血、炎症、血管生成以及动脉粥样硬化和癌症的病理生理学中发挥着重要作用。在本文中,我们揭示了一种机制,即作为活化蛋白C辅因子而广为人知的蛋白S,通过促进全长组织因子途径抑制剂(TFPI)与因子Xa(FXa)之间的相互作用来特异性抑制TF活性。蛋白S对TFPI抑制FXa的刺激作用是由FXa/TFPI复合物的抑制常数(K(i))降低10倍所致,该抑制常数在无蛋白S时为4.4 nM,在有蛋白S时降至0.5 nM。K(i)的这种降低不仅导致TF介导的凝血途径反馈抑制加速,而且还使有效抑制FXa所需的TFPI浓度处于血浆中TFPI浓度范围内。这一机制改变了血浆中TF诱导凝血酶形成的调节概念,并表明蛋白S和TFPI在抑制TF活性方面协同作用。我们的数据表明,蛋白S缺乏不仅通过损害蛋白C系统增加血栓形成风险,还通过降低TFPI下调外源性凝血途径的能力来增加血栓形成风险。