Objective:To determine the role of branched chain amino acid aminotransferase 1(BCAT1)in the survival of mesenchymal stem cells(MSCs);to explore the mechanism of BCAT1regulating MSCs survival.Methods:ADSCs were isolated from white adipose tissues of male Sprague Dawley rats.BCAT1 expression was knocked down or overexpressed in ADSCs by adenovirus transfection.ADSCs apoptosis was induced by hydrogen dioxide(H2O2)stimulation.ADSCs apoptosis was evaluated by CCK-8 cell viability assay,cleaved caspase-3expression,and TUNEL staining.The activity of P53 was suppressed by the specific inhibitor PFT-?in control or BCAT1 silencing ADSCs.Results:BCAT1,rather than BCAT2,was the predominant subtype expressed in ADSCs.Silencing of BCAT1 exacerbated,whereas BCAT1 overexpression ameliorated hydrogen dioxide-induced ADSCs apoptosis.The downstream targets of P53 were significantly increased in BCAT1 knock-downed ADSCs when stimulated by hydrogen dioxide.Inhibition of P53 by its specific inhibitor PFT-?reversed the adverse impact of BCAT1silencing on ADSCs survival.Conclusion:BCAT1 regulates ADSCs survival via a P53-dependent manner,revealing that BCAT1 is a promising target to enhance ADSCs survival and their cardioprotective efficacy. |