Caveolae internalization regulates integrin-dependent signaling pathways

被引:63
作者
Echarri, Asier [1 ]
Del Pozo, Miguel A. [1 ]
机构
[1] CNIC, Integrin Signaling Lab, E-28029 Madrid, Spain
关键词
integrins; membrane domains; Rho GTPases; signaling; anchorage-dependent growth; caveolin-1;
D O I
10.4161/cc.5.19.3264
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Integrin-mediated adhesion regulates trafficking of cholesterol-enriched membrane microdomains (CEMM). Upon cell detachment from the extracellular matrix (ECM), CEMMs undergo rapid internalization and are cleared from the plasma membrane. This pathway regulates integrin-mediated Rac membrane targeting, allowing coupling of Rac to downstream effectors. Internalization of CEMMs is mediated by Dynamin-2, a regulator of caveolae dynamics, and caveolin-1, an essential caveolae coat protein. Translocation of tyrosine phosphorylated caveolin-1 from focal adhesions to caveolae upon cell detachment induces CEMM internalization. Notably, integrin-mediated regulation of Erk, phosphatidylinositol-3-OH kinase (PI3K) and Rac pathways is dependent on caveolin-1. These results describe a novel pathway in which integrins prevent downregulation of Erk, PI3K and Rac-dependent pathways by inhibiting caveolin-1-dependent endocytosis. This pathway define a novel molecular mechanism for regulated cell growth and tumor suppression by caveolin-1.
引用
收藏
页码:2179 / 2182
页数:4
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