Embryonic stem cell-derived extracellular vesicles rejuvenate senescent cells and antagonize aging in mice

细胞生物学 小RNA 胚胎干细胞 基因沉默 干细胞 体内 转录组 生物 PI3K/AKT/mTOR通路 癌症研究 细胞外小泡 移植 表型 信号转导 医学 基因表达 基因 遗传学 内科学
作者
Yu Lu,Hang Wen,Chang Liu,Chen Wang,Huaxin Yu,Kaiyue Zhang,Qingsheng Han,Yue Liu,Zhongchao Han,Zongjin Li,Na Liu
出处
期刊:Bioactive Materials [Elsevier BV]
卷期号:29: 85-97 被引量:30
标识
DOI:10.1016/j.bioactmat.2023.06.011
摘要

Aging is a degenerative process that leads to tissue dysfunction and death. Embryonic stem cells (ESCs) have great therapeutic potential for age-related diseases due to their capacity for self-renewal and plasticity. However, the use of ESCs in clinical treatment is limited by immune rejection, tumourigenicity and ethical issues. ESC-derived extracellular vesicles (EVs) may provide therapeutic effects that are comparable to those of ESCs while avoiding unwanted effects. Here, we fully evaluate the role of ESC-EVs in rejuvenation in vitro and in vivo. Using RNA sequencing (RNA-Seq) and microRNA sequencing (miRNA-Seq) screening, we found that miR-15b-5p and miR-290a-5p were highly enriched in ESC-EVs, and induced rejuvenation by silencing the Ccn2-mediated AKT/mTOR pathway. These results demonstrate that miR-15b-5p and miR-290a-5p function as potent activators of rejuvenation mediated by ESC-EVs. The rejuvenating effect of ESC-EVs was further investigated in vivo by injection into aged mice. The results showed that ESC-EVs successfully ameliorated the pathological age-related phenotypes and rescued the transcriptome profile of aged mice. Our findings demonstrate that ESC-EVs treatment can rejuvenate senescence both in vitro and in vivo and suggest the therapeutic potential of ESC-EVs as a novel cell-free alternative to ESCs for age-related diseases.
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