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Embryonic stem cell-derived extracellular vesicles rejuvenate senescent cells and antagonize aging in mice.
- Source :
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Bioactive materials [Bioact Mater] 2023 Jul 01; Vol. 29, pp. 85-97. Date of Electronic Publication: 2023 Jul 01 (Print Publication: 2023). - Publication Year :
- 2023
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Abstract
- 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.<br />Competing Interests: The authors declare that there is no conflict of interest regarding the publication of this paper.<br /> (© 2023 The Authors.)
Details
- Language :
- English
- ISSN :
- 2452-199X
- Volume :
- 29
- Database :
- MEDLINE
- Journal :
- Bioactive materials
- Publication Type :
- Academic Journal
- Accession number :
- 37449253
- Full Text :
- https://doi.org/10.1016/j.bioactmat.2023.06.011