Differential Regulation of Adhesion Complex Turnover by ROCK1 and ROCK2.

FE Lock, KR Ryan, Natalie Poulter, M Parsons, Neil Hotchin

Research output: Contribution to journalArticlepeer-review

52 Citations (Scopus)
272 Downloads (Pure)

Abstract

BACKGROUND ROCK1 and ROCK2 are serine/threonine kinases that function downstream of the small GTP-binding protein RhoA. Rho signalling via ROCK regulates a number of cellular functions including organisation of the actin cytoskeleton, cell adhesion and cell migration. METHODOLOGY/PRINCIPAL FINDINGS In this study we use RNAi to specifically knockdown ROCK1 and ROCK2 and analyse their role in assembly of adhesion complexes in human epidermal keratinocytes. We observe that loss of ROCK1 inhibits signalling via focal adhesion kinase resulting in a failure of immature adhesion complexes to form mature stable focal adhesions. In contrast, loss of ROCK2 expression results in a significant reduction in adhesion complex turnover leading to formation of large, stable focal adhesions. Interestingly, loss of either ROCK1 or ROCK2 expression significantly impairs cell migration indicating both ROCK isoforms are required for normal keratinocyte migration. CONCLUSIONS ROCK1 and ROCK2 have distinct and separate roles in adhesion complex assembly and turnover in human epidermal keratinocytes.
Original languageEnglish
Pages (from-to)e31423
JournalPLoS ONE
Volume7
Issue number2
DOIs
Publication statusPublished - 1 Jan 2012

Fingerprint

Dive into the research topics of 'Differential Regulation of Adhesion Complex Turnover by ROCK1 and ROCK2.'. Together they form a unique fingerprint.

Cite this