Troponin I inhibits capillary endothelial cell proliferation by interaction with the cell's bFGF receptor

被引:31
作者
Feldman, L
Rouleau, C
机构
[1] Beth Israel Deaconess Med Ctr, Lab Cell & Mol Biol, Dept Med, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA 02215 USA
关键词
troponin I; angiogenesis inhibitors; bFGF receptors;
D O I
10.1006/mvre.2001.2364
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Troponin I (TnI) is a novel cartilage-derived angiogenesis inhibitor, first demonstrated by Moses et al. (1999, Proc. Natl. Acad. Sci. USA 96:2645-2650) to inhibit endothelial cell proliferation and angiogenesis, both in vivo and in vitro, and to inhibit metastasis of a wide variety of tumors in vivo. Despite convincing evidence of its efficacy, little is known about the mechanism of action of TnI as an anti-proliferative and anti-angiogenic agent. In the current article we demonstrate that TnI inhibits both bFGF-stimulated and basal levels of endothelial cell proliferation, and we hypothesize that this inhibition is occurring, at least in part, via an interaction of TnI with the cell-surface bFGF receptor on capillary endothelial cells. We further support this hypothesis by providing the first evidence that TnI can act on nonendothelial as well as endothelial cells and by demonstrating that this inhibitory action is specific for the bFGF receptor on the target cells. Preliminary data suggest that TnI may be competing with bFGF for interaction with the bFGF receptor on responsive cells. (C) 2001 Elsevier Science.
引用
收藏
页码:41 / 49
页数:9
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