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Ovarian aging increases small extracellular vesicle CD81+ release in human follicular fluid and influences miRNA profiles
Author(s) -
Rosalia Battaglia,
Paolo Musumeci,
Marco Ragusa,
Davide Barbagallo,
Marina Scalia,
Massimo Zimbone,
Maria José Lo Faro,
Placido Borzì,
Paolo Scollo,
Michele Purrello,
Elena Maria Vento,
Cinzia Di Pietro
Publication year - 2020
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.103441
Subject(s) - follicular fluid , cd81 , extracellular vesicles , vesicle , microrna , extracellular vesicle , extracellular , follicular phase , ovarian follicle , microvesicles , microbiology and biotechnology , chemistry , medicine , biology , immunology , oocyte , membrane , biochemistry , gene , embryo , hepatitis c virus , virus
Ovarian aging affects female reproductive potential and is characterized by alterations in proteins, mRNAs and non-coding RNAs inside the ovarian follicle. Ovarian somatic cells and the oocyte communicate with each other secreting different molecules into the follicular fluid, by extracellular vesicles. The cargo of follicular fluid vesicles may influence female reproductive ability; accordingly, analysis of extracellular vesicle content could provide information about the quality of the female germ cell.In order to identify the most significant deregulated microRNAs in reproductive aging, we quantified the small extracellular vesicles in human follicular fluid from older and younger women and analyzed the expression of microRNAs enclosed inside the vesicles. We found twice as many small extracellular vesicles in the follicular fluid from older women and several differentially expressed microRNAs. Correlating microRNA expression profiles with vesicle number, we selected 46 deregulated microRNAs associated with aging. Bioinformatic analyses allowed us to identify six miRNAs involved in TP53 signaling pathways. Specifically, miR-16-5p, miR214-3p and miR-449a were downregulated and miR-125b, miR-155-5p and miR-372 were upregulated, influencing vesicle release, oocyte maturation and stress response. We believe that this approach allowed us to identify a battery of microRNAs strictly related to female reproductive aging.

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