RPTP-α acts as a transducer of mechanical force on αv/β3-integrin–cytoskeleton linkages

Götz von Wichert(Columbia University), Guoying Jiang(Columbia University), Ana Kostić(Columbia University), Kurt J. De Vos(Columbia University), Jan Sap(New York University), Michael P. Sheetz(Columbia University)
The Journal of Cell Biology
April 7, 2003
Cited by 198Open Access
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Abstract

Cell motility on ECM critically depends on the cellular response to force from the matrix. We find that force-dependent reinforcement of alphav/beta3-integrin-mediated cell-matrix connections requires the receptor-like tyrosine phosphatase alpha (RPTPalpha). RPTPalpha colocalizes with alphav-integrins at the leading edge during early spreading, and coimmunoprecipitates with alphav-integrins during spreading on fibronectin and vitronectin. RPTPalpha-dependent activation of Src family kinases, in particular activation of Fyn, is required for the force-dependent formation of focal complexes and strengthening of alphav/beta3-integrin-cytoskeleton connections during the initial phase of ECM contact. These observations indicate that Src family kinases have distinct functions during adhesion site assembly, and that RPTPalpha is an early component in force-dependent signal transduction pathways leading to the assembly of focal complexes on both fibronectin and vitronectin.


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