Kindlin-2 controls bidirectional signaling of integrins

被引:349
作者
Montanez, Eloi [1 ]
Ussar, Siegfried [1 ]
Schifferer, Martina [1 ]
Boesl, Michael [1 ]
Zent, Roy [2 ,3 ]
Moser, Markus [1 ]
Faessler, Reinhard [1 ]
机构
[1] Max Planck Inst Biochem, Dept Mol Med, D-82152 Martinsried, Germany
[2] Vanderbilt Univ Sch Med, Dept Med, Div Nephrol, Nashville, TN 37232 USA
[3] Vet Affairs Hosp, Nashville, TN 37232 USA
关键词
integrin activation; Kindlin-2; adhesion; mouse development; embryonic stem cells;
D O I
10.1101/gad.469408
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Control of integrin activation is required for cell adhesion and ligand-induced signaling. Here we report that loss of the focal adhesion protein Kindlin-2 in mice results in peri-implantation lethality caused by severe detachment of the endoderm and epiblast from the basement membrane. We found that Kindlin-2-deficient cells were unable to activate their integrins and that Kindlin-2 is required for talin-induced integrin activation. Furthermore, we demonstrate that Kindlin-2 is required for integrin outside-in signaling to enable firm adhesion and spreading. Our findings provide evidence that Kindlin-2 is a novel and essential element of bidirectional integrin signaling.
引用
收藏
页码:1325 / 1330
页数:6
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