Kindlins: essential regulators of integrin signalling and cell-matrix adhesion

被引:208
作者
Larjava, Hannu [3 ]
Plow, Edward F. [2 ]
Wu, Chuanyue [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15261 USA
[2] Cleveland Clin, Dept Mol Cardiol, Cleveland, OH 44106 USA
[3] Univ British Columbia, Fac Dent, Vancouver, BC V5Z 1M9, Canada
关键词
cell adhesion; extracellular matrix; integrin; kindlin;
D O I
10.1038/embor.2008.202
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Integrin-mediated cell-ECM (extracellular matrix) adhesion is a fundamental process that controls cell behaviour. For correct cell-ECM adhesion, both the ligand-binding affinity and the spatial organization of integrins must be precisely controlled; how integrins are regulated, however, is not completely understood. Kindlins constitute a family of evolutionarily conserved cytoplasmic components of cell-ECM adhesions that bind to beta-integrin cytoplasmic tails directly and cooperate with talin in integrin activation. In addition, kindlins interact with many components of cell-ECM adhesions-such as migfilin and integrin-linked kinase-to promote cytoskeletal reorganization. Loss of kindlins causes severe defects in integrin signalling, cell-ECM adhesion and cytoskeletal organization, resulting in early embryonic lethality (kindlin-2), postnatal lethality (kindlin-3) and Kindler syndrome (kindlin-1). It is therefore clear that kindlins, together with several other integrin-proximal proteins, are essential for integrin signalling and cell-ECM adhesion regulation.
引用
收藏
页码:1203 / 1208
页数:6
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