蛋白质S从抗凝血剂到信号分子的历程。

JSM biochemistry and molecular biology Pub Date : 2016-01-01 Epub Date: 2016-08-08
V S Pilli, William Plautz, Rinku Majumder
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引用次数: 0

摘要

蛋白S (PS)是一种含γ-羧基谷氨酸的血清蛋白,于1977年被意外发现。发现后不久,PS因其在生理上的重要性而引起了研究人员的注意,它作为一种多功能蛋白,在血液凝固、炎症和其他细胞过程的交叉点上发挥作用。蛋白S通过直接抑制促凝剂,如Xa因子(FXa)、FVa和FIXa发挥抗凝作用,同时也作为活化蛋白C和组织因子途径抑制剂等抗凝剂的辅助因子。通过与C4b结合蛋白(C4BP)结合,PS也被证明可以最小化炎症的影响。最后,PS通过TAM家族蛋白激酶受体促进efferocytosis。PS基因突变可引起深静脉血栓形成和遗传性缺血等病理状况。本文就其多种功能的研究进展进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The Journey of Protein S from an Anticoagulant to a Signaling Molecule.

Protein S (PS), a γ-carboxyglutamate-containing serum protein, was unexpectedly discovered in 1977. Soon after its discovery, PS gained the attention of researchers because of its physiological importance, acting as a multifunctional protein at the intersection of blood coagulation, inflammation, and other cellular processes. Protein S functions as an anticoagulant by directly inhibiting procoagulants, such as Factor Xa (FXa), FVa, and FIXa, while also serving as a cofactor for anticoagulants such as Activated Protein C and Tissue Factor Pathway Inhibitor. By associating with C4b binding protein (C4BP), PS has also been shown to minimize the effect of inflammation. Finally, PS promotes efferocytosis through TAM family protein kinase receptors. Mutations in the PS gene cause pathological conditions such as deep vein thrombosis and hereditary ischemia. In this review, we summarize studies regarding the multiple functions of PS.

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