Endothelial cell-matrix interactions

被引:73
作者
Iivanainen, E
Kähäri, VM
Heino, J
Elenius, K
机构
[1] Turku Univ, Med Res Lab, FIN-20520 Turku, Finland
[2] Univ Turku, Dept Med Biochem & Mol Biol, FIN-20520 Turku, Finland
[3] Turku Univ, Turku Grad Sch Biomed Sci, FIN-20520 Turku, Finland
[4] Univ Turku, Turku Ctr Biotechnol, FIN-20520 Turku, Finland
[5] Abo Akad Univ, FIN-20520 Turku, Finland
[6] Turku Univ, Dept Dermatol, FIN-20520 Turku, Finland
[7] Univ Jyvaskyla, Dept Biol & Environm Sci, FIN-40351 Jyvaskyla, Finland
关键词
angiogenesis; extracellular matrix; glypican; integrin; matrix metalloprotein; syndecan;
D O I
10.1002/jemt.10238
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Dynamic interactions between endothelial cells and components of their surrounding extracellular matrix are necessary for the invasion, migration, and survival of endothelial cells during angiogenesis. These interactions are mediated by matrix receptors that initiate intracellular signaling cascades in response to binding to specific extracellular matrix molecules. The interactions between endothelial cells and their environment are also modulated by enzymes that degrade different matrix components and thus enable endothelial invasion. Recent reports on gene targeting in mice have confirmed the role of two classes of matrix receptors, integrins and cell surface heparan sulfate proteoglycans, and a group of matrix degrading proteolytic enzymes, matrix metalloproteinases, in angiogenesis. The significance of endothelial cell-matrix -interactions is further supported by several ongoing clinical trials that analyze the effects of drugs blocking this interaction on angiogenesis-dependent growth of human tumors. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:13 / 22
页数:10
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