The Rho GEFs LARG and GEF-H1 regulate the mechanical response to force on integrins

被引:293
作者
Guilluy, Christophe [1 ]
Swaminathan, Vinay [2 ]
Garcia-Mata, Rafael [1 ]
O'Brien, E. Timothy [3 ]
Superfine, Richard [3 ]
Burridge, Keith [1 ,4 ,5 ]
机构
[1] Univ N Carolina, Dept Cell & Dev Biol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Curriculum Appl Sci & Engn, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Phys & Astron, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, UNC McAllister Heart Inst, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
SIGNAL-TRANSDUCTION; FOCAL ADHESIONS; LIVING CELLS; MAP KINASE; RECRUITMENT; BINDING; STRESS; GAPS;
D O I
10.1038/ncb2254
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
How individual cells respond to mechanical forces is of considerable interest to biologists as force affects many aspects of cell behaviour(1). The application of force on integrins triggers cytoskeletal rearrangements and growth of the associated adhesion complex, resulting in increased cellular stiffness(2,3), also known as reinforcement(4). Although RhoA has been shown to play a role during reinforcement(3), the molecular mechanisms that regulate its activity are unknown. By combining biochemical and biophysical approaches, we identified two guanine nucleotide exchange factors (GEFs), LARG and GEF-H1, as key molecules that regulate the cellular adaptation to force. We show that stimulation of integrins with tensional force triggers activation of these two GEFs and their recruitment to adhesion complexes. Surprisingly, activation of LARG and GEF-H1 involves distinct signalling pathways. Our results reveal that LARG is activated by the Src family tyrosine kinase Fyn, whereas GEF-H1 catalytic activity is enhanced by ERK downstream of a signalling cascade that includes FAK and Ras.
引用
收藏
页码:722 / U211
页数:12
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