Oxidative stress influences cell survival and homeostasis,but the mechanisms underlying the biological effects of oxidative stress remain to be elucidated.The protein kinase MST1 plays a major role in oxidative stress-induced cell death in primary mammalian neurons.However,the mechanisms that regulate MST1 in oxidative stress responses remain largely unknown.In the present study,we demonstrate that the protein kinase c-Abl phosphorylates MST1 at Y433,which triggers the stabilization and activation of MST1.Inhibition of c-Abl promotes the degradation of MST1 through CHIP-mediated ubiquitination,and thereby attenuates cell death.Oxidative stress induces the c-Abl-dependent tyrosine phosphorylation of MST1 and increases the interaction between MST1 and FOXO3,thereby activating the MST1-FOXO signaling pathway,leading to cell death in both primary culture neurons and rat hippocampal neurons.The identification of the c-Abl tyrosine kinase as a novel upstream activator of MST1 suggests that the c-Abl-MST1 signaling cascade plays an important role in cellular responses to oxidative stress.