细胞外蛋白水解的生长因子控制

D.B. Rifkin , D. Moscatelli , J. Bizik , N. Quarto , F. Blei , P. Dennis , R. Flaumenhaft , P. Mignatti
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引用次数: 111

摘要

蛋白酶和生长因子在血管生成中的作用是复杂的。血管生成因子碱性成纤维细胞生长因子(bFGF)诱导内皮细胞中纤溶酶原激活剂和胶原酶的合成增加。此外,bFGF增加了细胞表面纤溶酶原激活物受体的数量。血浆纤溶酶的增加可能导致可溶性硫酸肝素-bFGF复合物的释放,这可能是bFGF的活性形式。血管生成的负调节因子转化生长因子β (TGF-β)的活性也受到蛋白酶的调节,因为TGF-β的释放潜伏形式被表面蛋白水解组装的纤溶酶原激活剂和纤溶酶激活。由于TGF-β诱导了纤溶酶原激活物的抑制剂,激活反应是自我调节的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Growth factor control of extracellular proteolysis

The involvement of proteases and growth factors in angiogenesis is complex. The angiogenic factor basic fibroblast growth factor (bFGF) induces increased synthesis of both plasminogen activator and collagenase in endothelial cells. In addition, bFGF increases the number of plasminogen activator receptors on the cell surface. Increased production of plasmin may be responsible for the release of soluble complexes of heparan sulfate-bFGF which may be the active form of bFGF. The activity of a negative regulator of angiogenesis, transforming growth factor β (TGF-β), is also regulated by proteases since the released latent form of TGF-β is activated by a surface proteolytic assembly plasminogen activator and plasmin. Since TGF-β induces an inhibitor of plasminogen activator, the activation reaction is self-regulatory.

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