下调和上调
自噬
氧化应激
细胞凋亡
衰老
细胞生物学
西妥因1
干细胞
化学
程序性细胞死亡
细胞
细胞生长
生物
生物化学
基因
作者
Tao Liu,Xiaojing Ma,Tao Ouyang,Huiping Chen,Jun Lin,Jun Li,Xinfeng Yan,Jie Yu,Yingying Huang
标识
DOI:10.1016/j.ijbiomac.2018.05.174
摘要
Stem cell senescence and exhaustion are considered important drivers of organismal aging, and human adipose-derived stem cells (ADSCs) have emerged as a promising cell source for cell-based therapy. However, aging and low survival rate compromise the optimal outcome of cell-based therapy due to oxidative stress in the graft areas. Oxidative stress has long been considered to be harmful to cells, nevertheless, in this study, we found that lower concentration of hydrogen peroxide (H2O2) decreased the number of SA-βgal-immunopositive cells, which was ameliorated by inhibition of SIRT1. Autophagy, a degradation mechanism that plays a major role in maintaining cellular homeostasis and, is involved in this effect. SIRT1 protein level in ADSCs was increased by the treatment with H2O2, meanwhile, H2O2 activated p53-depended apoptosis in high concentration. Incubation of ADSCs with H2O2 dose dependently induced ADSCs apoptosis. SIRT1 overexpression reduced the rate of ADSCs apoptosis, whereas SIRT1 downregulation and EX527 displayed the opposite effect. SIRT1 overexpression decreased the total p53 protein, whereas SIRT1 downregulation and EX527 increased the amount of p53 protein. Co-immunoprecipitation assay showed that SIRT1 could bind to p53, reduce its acetylation level, and treatment with nutlin-3A reversed the effect of SIRT1 on the level of p53 in ADSCs. These results suggest that SIRT1 had a pivotally protective role in the regulation of ADSCs aging and apoptosis induced by H2O2.
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