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因子IXa和血管性血友病因子可改变活化蛋白C对因子VIII的灭活作用。

Factor IXa and von Willebrand factor modify the inactivation of factor VIII by activated protein C.

作者信息

Rick M E, Esmon N L, Krizek D M

机构信息

Clinical Pathology Department, National Institutes of Health, Bethesda, MD 20892.

出版信息

J Lab Clin Med. 1990 Apr;115(4):415-21.

PMID:2109028
Abstract

Activated protein C inactivates factor VIII by proteolytic cleavage of the heavy chain of factor VIII. Protein S and calcium ions are cofactors in this reaction. We have examined the effects of several potential modulators of this reaction, including phospholipids, von Willebrand factor, and factor IXa, all of which bind factor VIII. Our results indicate that neither resting nor stimulated platelets nor phospholipid vesicles protect factor VIII from inactivation by activated protein C in either the presence or the absence of protein S. However, the addition of von Willebrand factor decreases the inactivation of factor VIII by activated protein C by 20% to 30%, and factor IXa, which is known to protect factor VIII from inactivation by activated protein C, confers additional protection with von Willebrand factor. The active site of factor IXa is necessary for the protective effect, because native factor IX and active site-inhibited factor IXa do not protect factor VIII from inactivation. Thus there is an additive protective effect when von Willebrand factor and factor IXa are present with factor VIII, leading to a decrease in the inactivation by activated protein C. These factors may be particularly important in stabilizing factor VIII in the circulation and during the early stages of coagulation.

摘要

活化蛋白C通过对凝血因子VIII重链的蛋白水解切割使其失活。蛋白S和钙离子是该反应的辅因子。我们研究了几种该反应潜在调节剂的作用,包括磷脂、血管性血友病因子和凝血因子IXa,它们均可结合凝血因子VIII。我们的结果表明,无论是静息还是活化的血小板,以及磷脂囊泡,在有或无蛋白S存在的情况下,均不能保护凝血因子VIII免受活化蛋白C的失活作用。然而,添加血管性血友病因子可使活化蛋白C对凝血因子VIII的失活作用降低20%至30%,而凝血因子IXa已知可保护凝血因子VIII免受活化蛋白C的失活作用,与血管性血友病因子共同作用时可提供额外保护。凝血因子IXa的活性位点对这种保护作用是必需的,因为天然凝血因子IX和活性位点被抑制的凝血因子IXa不能保护凝血因子VIII免受失活。因此,当血管性血友病因子和凝血因子IXa与凝血因子VIII同时存在时,会产生相加的保护作用,导致活化蛋白C的失活作用降低。这些因子在稳定循环中的凝血因子VIII以及凝血早期阶段可能尤为重要。

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