Haas T L, Madri J A
Department of Pathology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Trends Cardiovasc Med. 1999 Apr-May;9(3-4):70-7. doi: 10.1016/s1050-1738(99)00014-6.
The process of new blood vessel growth, angiogenesis, involves orchestrated alterations in endothelial cell interactions with adjacent cells and with components of the underlying basement membrane matrix. The activity of matrix metalloproteinases (MMPs), proteases that can cleave basement membrane and interstitial matrix molecules, has been shown to be necessary for angiogenesis as it occurs in several different in vivo and in vitro models. This review discusses the potential roles of two particular MMPs, MMP-2 and MT1-MMP, in angiogenesis, with emphasis on current understanding of how endothelial cell-extracellular matrix interactions may regulate the production of these MMPs via matrix-induced signaling leading to transcriptional activation and subsequent formation of active multiprotease complexes on the cell surface.
新血管生长的过程,即血管生成,涉及内皮细胞与相邻细胞以及与基底膜基质成分相互作用的精心协调的改变。基质金属蛋白酶(MMPs)是一类能够裂解基底膜和间质基质分子的蛋白酶,在多种不同的体内和体外模型中,其活性已被证明是血管生成所必需的。本综述讨论了两种特定的基质金属蛋白酶MMP-2和MT1-MMP在血管生成中的潜在作用,重点是当前对内皮细胞-细胞外基质相互作用如何通过基质诱导信号传导调节这些基质金属蛋白酶的产生的理解,这种信号传导导致转录激活以及随后在细胞表面形成活性多蛋白酶复合物。