The integrin αvβ8 mediates epithelial homeostasis through MT1-MMP-dependent activation of TGF-β1

被引:578
作者
Mu, DZ
Cambier, S
Fjellbirkeland, L
Baron, JL
Munger, JS
Kawakatsu, H
Sheppard, D
Broaddus, VC
Nishimura, SL
机构
[1] San Francisco Gen Hosp, Lung Biol Ctr, San Francisco, CA 94110 USA
[2] San Francisco Gen Hosp, Pulm Div, San Francisco, CA 94110 USA
[3] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Mt Zion Canc Ctr, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
基金
英国惠康基金;
关键词
integrins; transforming growth factor beta; metalloprotease; cell cycle; homeostasis;
D O I
10.1083/jcb.200109100
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Integrins, matrix metalloproteases (MMPs), and the cytokine TGF-beta have each been implicated in homeostatic cell behaviors such as cell growth and matrix remodeling. TGF-beta exists mainly in a latent state, and a major point of homeostatic control is the activation of TGF-beta. Because the latent domain of TGF-beta1 possesses an integrin binding motif (RGD), integrins have the potential to sequester latent TGF-beta (SLC) to the cell surface where TGF-beta activation could be locally controlled. Here, we show that SLC binds to alphavbeta8, an integrin expressed by normal epithelial and neuronal cells in vivo. This binding results in the membrane type 1 (MT1)-MMP-dependent release of active TGF-beta, which leads to autocrine and paracrine effects on cell growth and matrix production. These data elucidate a novel mechanism of cellular homeostasis achieved through the coordination of the activities of members of three major gene families involved in cell-matrix interactions.
引用
收藏
页码:493 / 507
页数:15
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