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C4b结合蛋白在活化蛋白C介导的因子VIIIa失活过程中,抑制蛋白S的因子V依赖性辅因子活性,但不抑制其因子V非依赖性辅因子活性。

C4b-binding protein inhibits the factor V-dependent but not the factor V-independent cofactor activity of protein S in the activated protein C-mediated inactivation of factor VIIIa.

作者信息

van de Poel R H, Meijers J C, Bouma B N

机构信息

Department of Haematology, University Medical Center, Utrecht, The Netherlands.

出版信息

Thromb Haemost. 2001 May;85(5):761-5.

Abstract

Activated protein C (APC) is an important inactivator of coagulation factors Va and VIIIa. In the inactivation of factors Va and VIIIa, protein S serves as a cofactor to APC. Protein S can bind to C4b-binding protein (C4BP), and thereby loses its cofactor activity to APC. By modulating free protein S levels, C4BP is an important regulator of protein S cofactor activity. In the factor VIIIa inactivation, protein S and factor V act as synergistic cofactors to APC. We investigated the effect of C4BP on both the factor V-independent and factor V-dependent cofactor activity of protein S in the factor VIIIa inactivation using a purified system. Protein S increased the APC-mediated inactivation of factor VIIIa to 60% and in synergy with protein S, factor V at equimolar concentrations increased this effect further to 90%. The protein S/factor V synergistic effect was inhibited by preincubation of protein S and factor V with a four-fold molar excess of C4BP. However, C4BP did not inhibit the factor V-independent protein S cofactor activity in the purified system whereas it inhibited the cofactor activity in plasma. We conclude that C4BP-bound protein S retains its cofactor activity to APC in the factor VIIIa inactivation.

摘要

活化蛋白C(APC)是凝血因子Va和VIIIa的重要灭活剂。在因子Va和VIIIa的灭活过程中,蛋白S作为APC的辅因子。蛋白S可与C4b结合蛋白(C4BP)结合,从而失去其对APC的辅因子活性。通过调节游离蛋白S水平,C4BP是蛋白S辅因子活性的重要调节剂。在因子VIIIa的灭活过程中,蛋白S和因子V作为APC的协同辅因子。我们使用纯化系统研究了C4BP对因子VIIIa灭活中蛋白S的不依赖因子V和依赖因子V的辅因子活性的影响。蛋白S将APC介导的因子VIIIa灭活提高到60%,并且与蛋白S协同作用,等摩尔浓度的因子V将这种作用进一步提高到90%。蛋白S/因子V的协同作用被蛋白S和因子V与四倍摩尔过量的C4BP预孵育所抑制。然而,在纯化系统中C4BP并未抑制不依赖因子V的蛋白S辅因子活性,而在血浆中它抑制了辅因子活性。我们得出结论,在因子VIIIa灭活过程中,与C4BP结合的蛋白S保留了其对APC的辅因子活性。

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