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Int J Biochem Cell Biol. 2010 May;42(5):595-603. doi: 10.1016/j.biocel.2009.10.015. Epub 2009 Oct 23.

The role of kindlins in cell biology and relevance to human disease.

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1
St John's Institute of Dermatology, King's College London (Guy's Campus), London, United Kingdom.

Abstract

The kindlins represent a class of focal adhesion proteins implicated in integrin activation. They comprise three evolutionarily conserved members, kindlin-1, kindlin-2 and kindlin-3, that share considerable sequence and structural similarities. The kindlins have a bipartite FERM (four point one protein, ezrin, radixin, moesin) domain interrupted by a pleckstrin homology domain and can bind directly to various classes of integrins as well as participate in inside-out integrin activation. They are encoded by three different genes, namely KIND1 (FERMT1; chromosome 20p12.3), KIND2 (FERMT2; chromosome 14q22.1) and KIND3 (FERMT3; chromosome 11q13.1). Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology. In this review, we focus on the cellular functions of the kindlins and their clinical relevance.

PMID:
19854292
DOI:
10.1016/j.biocel.2009.10.015
[Indexed for MEDLINE]

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