A mechanism for modulation of cellular responses to VEGF: Activation of the integrins

被引:377
作者
Byzova, TV
Goldman, CK
Pampori, N
Thomas, KA
Bett, A
Shattil, SJ
Plow, EF
机构
[1] Cleveland Clin Fdn, Joseph J Jacobs Ctr Thrombosis & Vasc Biol, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Dept Mol Cardiol, Cleveland, OH 44195 USA
[3] Cleveland Clin Fdn, Dept Cell Biol, Cleveland, OH 44195 USA
[4] Scripps Res Inst, Dept Vasc Biol, La Jolla, CA 92037 USA
[5] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[6] Merck Res Labs, Dept Canc Res, W Point, PA 19486 USA
关键词
D O I
10.1016/S1097-2765(05)00076-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many similarities exist in the cellular responses elicited by VEGF and governed by integrins. Here, we identify a basis for these interrelationships: VEGF activates integrins. VEGF enhanced cell adhesion, migration, soluble ligand binding, and adenovirus gene transfer mediated by alpha (v)beta (3) and also activated other integrins, alpha (v)beta (5), alpha (5)beta (1), and alpha (2)beta (1), involved in angiogenesis. Certain tumor cells exhibited high spontaneous adhesion and migration, which were attributable to a VEGF-dependent autocrine/paracrine activation of integrins. This activation was mediated by the VEGFR2 receptor and regulated via phosphatidylinositol-3-kinase, Akt, and the PTEN signaling axis. Thus, integrin activation provides a mechanism for VEGF to induce a broad spectrum of cellular responses.
引用
收藏
页码:851 / 860
页数:10
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