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ABSTRACT: Background
We have previously shown that SHP2 downregulation may predispose fibroblasts to differentiate into myofibroblasts and proposed a role for SHP2 downregulation in the pathogenesis of idiopathic pulmonary fibrosis (IPF). Recent data have shown that SHP2 localizes to the mitochondrial intercristae, and its overexpression enhances mitochondrial metabolism leading to oxidative stress and senescence.Objective
To determine the effect of SHP2 on fibrotic responses.Methods and results
Primary mouse lung fibroblasts derived from mice carrying a conditional knock-in mutation (D61G/+), rendering the SHP2 catalytic domain constitutively active, had reduced proliferation (1.6-fold, p < 0.05), migration (2-fold, p < 0.05), as well as reduced responsiveness
SUBMITTER: Karampitsakos T
PROVIDER: S-EPMC10047203 | biostudies-literature | 2023 Mar
REPOSITORIES: biostudies-literature