Role of uPA/uPAR in the modulation of angiogenesis.

Chemical immunology and allergy Pub Date : 2014-01-01 Epub Date: 2013-10-17 DOI:10.1159/000353310
Nunzia Montuori, Pia Ragno
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引用次数: 56

Abstract

Blood vessels connect all districts of the body and allow blood oxygen and nutrients to reach every cell in the organism. Dysregulation of blood vessel formation or functionality is the origin of a large number of diseases. During new vessel formation, endothelial cells degrade their basement membrane, migrate into the interstitial matrix and proliferate. Migrating endothelial cells need to be polarized, to focus at their leading edge the proteolytic machinery, which is essential for extracellular matrix degradation; thus, proteases and their receptors play a crucial role in angiogenesis. The urokinase-mediated plasminogen activation system is a complex system of serine proteases strongly involved in angiogenesis. The plasminogen activation system includes plasminogen/plasmin, activators, inhibitors and cell receptors. In the last decades, a large body of evidence has clearly indicated that the role of this system is not limited to extracellular matrix proteolysis but can contribute to all phases of the angiogenic process.

uPA/uPAR在血管生成调控中的作用。
血管连接身体的各个部位,使血液中的氧气和营养物质到达机体的每一个细胞。血管形成或功能失调是许多疾病的起源。在新血管形成过程中,内皮细胞降解其基底膜,迁移到间质基质中并增殖。迁移的内皮细胞需要极化,聚焦于其前沿的蛋白水解机制,这是细胞外基质降解所必需的;因此,蛋白酶及其受体在血管生成中起着至关重要的作用。尿激酶介导的纤溶酶原激活系统是一个复杂的丝氨酸蛋白酶系统,与血管生成密切相关。纤溶酶原激活系统包括纤溶酶原/纤溶酶、激活剂、抑制剂和细胞受体。在过去的几十年里,大量证据清楚地表明,该系统的作用不仅限于细胞外基质蛋白水解,而且可以参与血管生成过程的所有阶段。
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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