Montanez Eloi, Ussar Siegfried, Schifferer Martina, Bösl Michael, Zent Roy, Moser Markus, Fässler Reinhard
Department of Molecular Medicine, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
Genes Dev. 2008 May 15;22(10):1325-30. doi: 10.1101/gad.469408.
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.
整合素激活的调控对于细胞黏附和配体诱导的信号传导是必需的。在此我们报告,小鼠中黏着斑蛋白Kindlin-2的缺失导致着床前致死,这是由内胚层和外胚层从基底膜严重脱离所致。我们发现Kindlin-2缺陷型细胞无法激活其整合素,并且Kindlin-2是踝蛋白诱导的整合素激活所必需的。此外,我们证明Kindlin-2是整合素外向内信号传导所必需的,以实现牢固黏附和铺展。我们的研究结果提供了证据,表明Kindlin-2是双向整合素信号传导的一个新的必需元件。