Sottile Jane
Center for Cardiovascular Research, Department of Medicine, University of Rochester Medical Center, 601 Elmwood Avenue, Box 679, Rochester, NY 14642, USA.
Biochim Biophys Acta. 2004 Mar 4;1654(1):13-22. doi: 10.1016/j.bbcan.2003.07.002.
During angiogenesis, endothelial cell growth, migration, and tube formation are regulated by pro- and anti-angiogenic factors, matrix-degrading proteases, and cell-extracellular matrix interactions. Temporal and spatial regulation of extracellular matrix remodeling events allows for local changes in net matrix deposition or degradation, which in turn contributes to control of cell growth, migration, and differentiation during different stages of angiogenesis. Remodeling of the extracellular matrix can have either pro- or anti-angiogenic effects. Extracellular matrix remodeling by proteases promotes cell migration, a critical event in the formation of new vessels. Matrix-bound growth factors released by proteases and/or by angiogenic factors promote angiogenesis by enhancing endothelial migration and growth. Extracellular matrix molecules, such as thrombospondin-1 and -2, and proteolytic fragments of matrix molecules, such as endostatin, can exert anti-angiogenic effects by inhibiting endothelial cell proliferation, migration and tube formation. In contrast, other matrix molecules promote endothelial cell growth and morphogenesis, and/or stabilize nascent blood vessels. Hence, extracellular matrix molecules and extracellular matrix remodelling events play a key role in regulating angiogenesis.
在血管生成过程中,内皮细胞的生长、迁移和管腔形成受促血管生成因子和抗血管生成因子、基质降解蛋白酶以及细胞与细胞外基质相互作用的调节。细胞外基质重塑事件的时空调节使得净基质沉积或降解发生局部变化,进而有助于在血管生成的不同阶段控制细胞生长、迁移和分化。细胞外基质的重塑可产生促血管生成或抗血管生成作用。蛋白酶介导的细胞外基质重塑促进细胞迁移,这是新血管形成中的关键事件。蛋白酶和/或血管生成因子释放的与基质结合的生长因子通过增强内皮细胞迁移和生长来促进血管生成。细胞外基质分子,如血小板反应蛋白-1和-2,以及基质分子的蛋白水解片段,如内皮抑素,可通过抑制内皮细胞增殖、迁移和管腔形成发挥抗血管生成作用。相反,其他基质分子促进内皮细胞生长和形态发生,和/或稳定新生血管。因此,细胞外基质分子和细胞外基质重塑事件在调节血管生成中起关键作用。