Sirtuin3 protects aged human mesenchymal stem cells against oxidative stress and enhances efficacy of cell therapy for ischaemic heart diseases

• DOI: 10.1111/jcmm.13821
• Publication Date: 2018-08-09T12:56:08Z
• Authors: Dong‐Yang Zhang; Chun‐Feng Zhang; Bi‐Cheng Fu; Lu Sun; Xue‐Qing Wang; Wei Chen; Wei Liu; Kai‐Yu Liu; Guo‐Qing Du; Chong‐Yi Ma; Shu‐Lin Jiang; Ren‐Ke Li; Hai Tian
• Keywords: Aging; 0303 health sciences; Superoxide Dismutase; Forkhead Box Protein O3; Cell- and Tissue-Based Therapy; Myocardial Infarction; Myocardial Ischemia; Gene Expression Regulation, Developmental; Mesenchymal Stem Cells; Original Articles; Catalase; Mesenchymal Stem Cell Transplantation; Protective Agents; Antioxidants; Rats; 3. Good health; Oxidative Stress; 03 medical and health sciences; Bone Marrow; Sirtuin 3; Animals; Humans; Reactive Oxygen Species; Plasmids

AbstractSirtuin3 (SIRT3) is associated with oxidative stress and lifespan. However, the possible mechanisms underlying its influence are unknown. We hypothesized that SIRT3 increases the antioxidant capacity of aged cells and improves the efficacy of human mesenchymal stem cell (hMSC) therapy for ischaemic heart diseases in aged patients. In vitro, the antioxidant capacity of old hMSCs (O‐hMSCs) was increased after SIRT3 overexpression using a gene transfection technique, while the antioxidant capacity of young hMSCs (Y‐hMSCs) was decreased by SIRT3 silencing. The levels of forkhead box O3a (FoxO3a) in the nucleus, and antioxidant enzymes Mn‐superoxide dismutase (MnSOD) and catalase (CAT) increased in SIRT3‐overexpressed O‐hMSCs while they decreased in SIRT3‐silenced Y‐hMSCs after oxidative stress. Following myocardial infarction in adult rats in vivo, infarct size decreased and cardiac function was significantly enhanced after cell transplantation with SIRT3 overexpressed O‐hMSCs. The number of apoptotic cells decreased and the survival rate of transplanted cells increased following SIRT3 overexpression in O‐hMSCs. SIRT3 protects aged hMSCs against oxidative stress by positively regulating antioxidant enzymes (MnSOD and CAT) via increasing the expression of FoxO3a in the nucleus. The efficacy of aged hMSC transplantation therapy for ischaemic heart diseases can be improved by SIRT3 overexpression.