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细胞外蛋白水解的生长因子调控

Growth factor control of extracellular proteolysis.

作者信息

Rifkin D B, Moscatelli D, Bizik J, Quarto N, Blei F, Dennis P, Flaumenhaft R, Mignatti P

机构信息

Department of Cell Biology, New York University Medical Center, NY 10016.

出版信息

Cell Differ Dev. 1990 Dec 2;32(3):313-8. doi: 10.1016/0922-3371(90)90045-x.

Abstract

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 beta (TGF-beta), is also regulated by proteases since the released latent form of TGF-beta is activated by a surface proteolytic assembly plasminogen activator and plasmin. Since TGF-beta induces an inhibitor of plasminogen activator, the activation reaction is self-regulatory.

摘要

蛋白酶和生长因子在血管生成中的作用十分复杂。血管生成因子碱性成纤维细胞生长因子(bFGF)可诱导内皮细胞中纤溶酶原激活物和胶原酶的合成增加。此外,bFGF还可增加细胞表面纤溶酶原激活物受体的数量。纤溶酶产量的增加可能与硫酸乙酰肝素 - bFGF可溶性复合物的释放有关,而该复合物可能是bFGF的活性形式。血管生成负调节因子转化生长因子β(TGF-β)的活性也受蛋白酶调节,因为释放的潜伏形式的TGF-β可被表面蛋白水解复合物纤溶酶原激活物和纤溶酶激活。由于TGF-β可诱导纤溶酶原激活物的抑制剂产生,所以激活反应具有自我调节作用。

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