Talins and kindlins: partners in integrin-mediated adhesion

被引:500
作者
Calderwood, David A. [1 ,2 ]
Campbell, Iain D. [3 ]
Critchley, David R. [4 ]
机构
[1] Yale Univ, Sch Med, Dept Pharmacol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06520 USA
[3] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
[4] Univ Leicester, Dept Biochem, Leicester LE1 7RH, Leics, England
基金
英国医学研究理事会; 美国国家卫生研究院; 英国惠康基金;
关键词
PLECKSTRIN HOMOLOGY DOMAIN; VINCULIN-BINDING-SITE; UBIQUITIN-LIKE DOMAIN; STRUCTURAL BASIS; CELL-ADHESION; IN-VIVO; EXTRACELLULAR-MATRIX; CYTOPLASMIC DOMAIN; FILAMIN-BINDING; FOCAL ADHESIONS;
D O I
10.1038/nrm3624
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Integrin receptors provide a dynamic, tightly-regulated link between the extracellular matrix (or cellular counter-receptors) and intracellular cytoskeletal and signalling networks, enabling cells to sense and respond to their chemical and physical environment. Talins and kindlins, two families of FERM-domain proteins, bind the cytoplasmic tail of integrins, recruit cytoskeletal and signalling proteins involved in mechano-transduction and synergize to activate integrin binding to extracellular ligands. New data reveal the domain structure of full-length talin, provide insights into talin-mediated integrin activation and show that RIAM recruits talin to the plasma membrane, whereas vinculin stabilizes talin in cell-matrix junctions. How kindlins act is less well-defined, but disease-causing mutations show that kindlins are also essential for integrin activation, adhesion, cell spreading and signalling.
引用
收藏
页码:503 / 517
页数:15
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