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蛋白S从抗凝剂到信号分子的历程。

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

作者信息

Pilli V S, Plautz William, Majumder Rinku

机构信息

Department of Biochemistry & Molecular Biology, LSU Health Science Center, USA.

出版信息

JSM Biochem Mol Biol. 2016;3(1). Epub 2016 Aug 8.

Abstract

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.

摘要

蛋白S(PS)是一种含γ-羧基谷氨酸的血清蛋白,于1977年意外发现。发现后不久,PS因其生理重要性引起了研究人员的关注,它在血液凝固、炎症和其他细胞过程的交叉点发挥多功能蛋白的作用。蛋白S通过直接抑制凝血因子,如因子Xa(FXa)、FVa和FIXa,发挥抗凝作用,同时还作为抗凝蛋白如活化蛋白C和组织因子途径抑制物的辅因子。通过与C4b结合蛋白(C4BP)结合,PS也被证明可将炎症的影响降至最低。最后,PS通过TAM家族蛋白激酶受体促进吞噬作用。PS基因的突变会导致诸如深静脉血栓形成和遗传性缺血等病理状况。在本综述中,我们总结了关于蛋白S多种功能的研究。

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