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Syndecan-1 controls cell migration by activating Rap1 to regulate focal adhesion disassembly
Author(s) -
William A. Altemeier,
Saundra Y. Schlesinger,
Catherine A. Buell,
William C. Parks,
Peter Chen
Publication year - 2012
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.109884
Subject(s) - focal adhesion , microbiology and biotechnology , biology , syndecan 1 , rap1 , adhesion , cell adhesion , cell migration , cell , cell adhesion molecule , signal transduction , biochemistry , chemistry , organic chemistry
After injury, residual epithelial cells coordinate contextual clues from cell-cell and cell-matrix interactions to polarize and migrate over the wound bed. Protrusion formation, cell body translocation and rear retraction is a repetitive process that allows the cell to move across the substratum. Fundamental to this process is the assembly and disassembly of focal adhesions that facilitate cell adhesion and protrusion formation. Here, we identified syndecan-1 as a regulator of focal adhesion disassembly in migrating lung epithelial cells. Syndecan-1 altered the dynamic exchange of adhesion complex proteins, which in turn regulates migration speed. Moreover, we provide evidence that syndecan-1 controls this entire process through Rap1. Thus, syndecan-1 restrains migration in lung epithelium by activating Rap1 to slow focal adhesion disassembly.

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