BACKGROUND: Patients with diminished ovarian reserve (DOR) significantly reduced success rates in assisted reproduction, making DOR a major clinical challenge in assisted reproductive technologies. Recent studies have indicated that extracellular vesicles (EVs) derived from mesenchymal stem cells (MSCs) hold promise for improving ovarian function, yet the impact of tissue origin on EVs function remains unclear. Adipose tissue and the umbilical cord are common and easily accessible sources of MSCs. This study aimed to compare the therapeutic effects of adipose-derived MSC- EVs (A-EVs) and umbilical cord MSC- EVs (U-EVs) in a cyclophosphamide-induced DOR mouse model, investigate their underlying mechanisms and provide experimental evidence for selecting the most promising EVs source for clinical application. RESULTS: Proteomic analysis revealed differences protein composition between U-EVs and A-EVs. Both A-EVs and U-EVs significantly increased serum AMH levels and improved fertility, whereas U-EVs produced more sustained reproductive benefits. Single-cell RNA sequencing and in vitro functional validation demonstrated that EV treatment reduced granulosa-cell apoptosis, oxidative stress, DNA-damage responses, and senescence signatures, with U-EVs exerting broader regulatory effects. CONCLUSIONS: In conclusion, both A-EVs and U-EVs improved ovarian function in DOR mice; however, U-EVs demonstrated greater efficacy in promoting long-term fertility and inhibiting granulosa cell apoptosis, indicating greater potential for clinical translation.
Li et al. (Wed,) studied this question.