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内皮细胞上依赖于凝血因子 XII 的接触激活以及结合蛋白 gC1qR 和细胞角蛋白 1。

Factor XII-dependent contact activation on endothelial cells and binding proteins gC1qR and cytokeratin 1.

作者信息

Joseph K, Shibayama Y, Ghebrehiwet B, Kaplan A P

机构信息

Department of Medicine and Konishi-MUSC Institute for Inflammation Research, Medical University of South Carolina, Charleston 29425, USA.

出版信息

Thromb Haemost. 2001 Jan;85(1):119-24.

Abstract

Although proteins of the kinin-forming pathway are bound along the surface of endothelial cells, the mechanism of activation of this proteolytic cascade is unclear. Endothelial cell surface proteins, gC1qR and cytokeratin 1, are capable of binding Factor XII and high molecular weight kininogen (HK) in a zinc-dependent reaction thus we considered the possibility that these proteins might catalyze initiation of the cascade. Incubation of Factor XII, prekallikrein, and HK with gC1qR or cytokeratin 1 leads to a zinc-dependent and Factor XII-dependent conversion of prekallikrein to kallikrein. We also demonstrate that normal plasma is capable of activating upon interaction with the cells whereas plasma deficient in Factor XII, prekallikrein and HK do not activate. Normal plasma activation was inhibitable by antibody to gC1qR and cytokeratin 1. Thus, gC1qR and cytokeratin 1, represent potential initiating surfaces for activation of the plasma kinin-forming cascade and may do so as a result of their expression along cell surfaces.

摘要

尽管激肽形成途径的蛋白质沿内皮细胞表面结合,但这种蛋白水解级联反应的激活机制尚不清楚。内皮细胞表面蛋白gC1qR和细胞角蛋白1能够在锌依赖性反应中结合因子XII和高分子量激肽原(HK),因此我们考虑了这些蛋白可能催化级联反应起始的可能性。将因子XII、前激肽释放酶和HK与gC1qR或细胞角蛋白1一起孵育会导致前激肽释放酶在锌依赖性和因子XII依赖性作用下转化为激肽释放酶。我们还证明,正常血浆在与细胞相互作用时能够被激活,而缺乏因子XII、前激肽释放酶和HK的血浆则不能被激活。正常血浆的激活可被抗gC1qR和细胞角蛋白1的抗体抑制。因此,gC1qR和细胞角蛋白1代表了血浆激肽形成级联反应激活的潜在起始表面,并且可能由于它们沿细胞表面的表达而起到这样的作用。

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