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内皮细胞对纤溶酶原激活物合成与分泌的调节。

Regulation of the synthesis and secretion of plasminogen activators by endothelial cells.

作者信息

van Hinsbergh V W

机构信息

Gaubius Institute TNO, Leiden, The Netherlands.

出版信息

Haemostasis. 1988;18(4-6):307-27. doi: 10.1159/000215814.

Abstract

Plasminogen activators (PAs) play a role in fibrinolysis, tissue remodelling, tumor invasion, and reparative processes. Vascular endothelial cells produce tissue-type PA (t-PA), an important regulator of fibrinolysis, and PA inhibitor 1. They can also synthesize a second type of PA, urokinase-type PA (u-PA). The regulation of synthesis and secretion of these PAs by human and bovine endothelial cells in vitro is reviewed. The synthesis of t-PA and u-PA varies between endothelial cells, depending on their vascular origin. The production of PA activity by endothelial cells is regulated at various levels: (1) induction of newly synthesized t-PA or u-PA molecules; (2) rapid release of t-PA from endothelial cells; (3) conversion of single-chain u-PA in the more active two-chain u-PA; (4) interaction of PAs with cellular receptors and matrix components, and (5) interaction of PAs with specific inhibitors.

摘要

纤溶酶原激活剂(PAs)在纤维蛋白溶解、组织重塑、肿瘤侵袭和修复过程中发挥作用。血管内皮细胞产生组织型PA(t-PA),这是纤维蛋白溶解的重要调节因子,以及PA抑制剂1。它们还能合成第二种PA,即尿激酶型PA(u-PA)。本文综述了人源和牛源内皮细胞在体外对这些PA的合成和分泌的调节。t-PA和u-PA的合成在不同的内皮细胞之间存在差异,这取决于它们的血管起源。内皮细胞产生PA活性的过程在多个层面受到调节:(1)新合成的t-PA或u-PA分子的诱导;(2)t-PA从内皮细胞的快速释放;(3)单链u-PA向活性更高的双链u-PA的转化;(4)PA与细胞受体和基质成分的相互作用,以及(5)PA与特异性抑制剂的相互作用。

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