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MSCs-derived EVs protect against chemotherapy-induced ovarian toxicity: role of PI3K/AKT/mTOR axis.
- Source :
-
Journal of ovarian research [J Ovarian Res] 2024 Nov 11; Vol. 17 (1), pp. 222. Date of Electronic Publication: 2024 Nov 11. - Publication Year :
- 2024
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Abstract
- Chemotherapy detrimentally impacts fertility via depletion of follicular reserves in the ovaries leading to ovarian failure (OF) and development of estrogen deficiency-related complications. The currently proposed options to preserve fertility such as Oocyte or ovarian cortex cryopreservation are faced with many technical obstacles that limit their effective implementation. Therefore, developing new modalities to protect ovarian function remains a pending target. Exosomes are nano-sized cell-derived extracellular vesicles (EVs) with documented efficacy in the field of regenerative medicine. The current study sought to determine the potential beneficial effects of mesenchymal stem cells (MSCs)-derived EVs in experimentally induced OF. Female albino rats were randomly allocated to four groups: control, OF group, OF + MSCs-EVs group, OF + Rapamycin (mTOR inhibitor) group, and OF + Quercetin (PI3K/AKT inhibitor) group. Follicular development was assessed via histopathological and immunohistochemical examination, and ovarian function was evaluated by hormonal assay. PI3K/Akt/mTOR signaling pathway as a key modulator of ovarian follicular activation was also assessed. MSCs-EVs administration to OF rats resulted in restored serum hormonal levels, preserved primordial follicles and oocytes, suppressed ovarian PI3K/AKT axis and downstream effectors (mTOR and FOXO3), modulated miRNA that target this axis, decreased expression of ovarian apoptotic markers (BAX, BCl2) and increased expression of proliferation marker Ki67. The present study validated the effectiveness of MSCs-EVs therapy in preventing ovarian insufficiency induced by chemotherapy. Concomitant MSCs-EVs treatment during chemotherapy could significantly preserve ovarian function and fertility by suppressing the PI3K/Akt axis, preventing follicular overactivation, maintaining normal ovarian cellular proliferation, and inhibiting granulosa cell apoptosis.<br />Competing Interests: Declarations Institutional review board statement The experimental procedure was conducted in compliance with the National Institutes of Health’s Guide for the Care and Use of Laboratory Animals (NIH publication No. 85–23, revised 2011) and carried out following the institutional review board for animal experiments of the Faculty of Medicine, Benha University, Egypt (BUFVTM 07-07-22). Competing interests The authors declare no competing interests.<br /> (© 2024. The Author(s).)
- Subjects :
- Female
Animals
Rats
Extracellular Vesicles metabolism
Extracellular Vesicles drug effects
Antineoplastic Agents pharmacology
Primary Ovarian Insufficiency chemically induced
Primary Ovarian Insufficiency metabolism
Primary Ovarian Insufficiency prevention & control
Apoptosis drug effects
TOR Serine-Threonine Kinases metabolism
Proto-Oncogene Proteins c-akt metabolism
Mesenchymal Stem Cells metabolism
Mesenchymal Stem Cells drug effects
Ovary drug effects
Ovary metabolism
Signal Transduction drug effects
Phosphatidylinositol 3-Kinases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1757-2215
- Volume :
- 17
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of ovarian research
- Publication Type :
- Academic Journal
- Accession number :
- 39529187
- Full Text :
- https://doi.org/10.1186/s13048-024-01545-7