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Efficacy of extracellular vesicles derived from mesenchymal stromal cells in regulating senescence: In vitro and in vivo insights

间充质干细胞 细胞生物学 细胞外小泡 化学 氧化应激 衰老 间质细胞 细胞外 小泡 细胞衰老 微泡 氧化磷酸化 胞外囊泡 细胞内 氧化损伤 外体 生物化学 内体
作者
Shuang-Shuang Yang,Siyu Chen,Wen-Ya Zhuang,Jing Han,Ya Liu,Li Deng,Huizhen Guo,He-Ran Ma,Yi Tan
出处
期刊:World Journal of Stem Cells [Baishideng Publishing Group]
卷期号:17 (10): 110445-110445 被引量:4
标识
DOI:10.4252/wjsc.v17.i10.110445
摘要

BACKGROUND Extracellular vesicles derived from mesenchymal stromal cells (MSC-EVs) can be used for anti-aging therapy and treating various aging-related diseases. However, the clinical application of MSC-EVs is still limited, mainly due to insufficient information on the preparation process, quality, and mechanism of action of MSC-EVs. AIM To study the biological effects of MSC-EVs in regulating cellular senescence. METHODS In this study, we developed a clinical-grade production process for MSC-EVs and defined the release criteria for products suitable for human use. To support the clinical use of our product as a therapeutic agent, we performed efficacy assays to evaluate the anti-aging capacity of MSC-EVs in vitro and in vivo . RESULTS The functional analysis results revealed that MSC-EVs significantly reduced the levels of senescence-associated β-galactosidase, matrix metallopeptidase 1, P21, and interleukin-1β and increased the level of collagen I in a naturally aged cell model of human dermal fibroblasts. Similarly, treatment with MSC-EVs effectively improved D-gal-induced subacute aging in mice, aging-related histopathological changes, oxidative stress, and aging-related gene expression. CONCLUSION These findings indicate that MSC-EVs can partially alleviate D-gal-induced senescence by reducing oxidative stress and regulating metabolism. Overall, these findings strongly suggest that MSC-EVs hold promise for aging therapy.
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