SHP-2 is activated in response to force on E-cadherin and dephosphorylates vinculin Y822.

ABSTRACT: The response of cells to mechanical inputs is a key determinant of cell behavior. In response to external forces, E-cadherin initiates signal transduction cascades that allow the cell to modulate its contractility to withstand the force. Much attention has focused on identifying the E-cadherin signaling pathways that promote contractility, but the negative regulators remain undefined. In this study, we identify SHP-2 as a force-activated phosphatase that negatively regulates E-cadherin force transmission by dephosphorylating vinculin Y822. To specifically probe a role for SHP-2 in E-cadherin mechanotransduction, we mutated vinculin so that it retains its phosphorylation but cannot be dephosphorylated. Cells expressing the mutant vinculin have increased contractility. This work provides a m

SUBMITTER: Campbell H 

PROVIDER: S-EPMC6307880 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature