Human follicular fluid elicits select dose- and age-dependent effects on mouse oocytes and cumulus–oocyte complexes in a heterologous in vitro maturation assay

Author:

Dipali Shweta S1ORCID,Suebthawinkul Chanakarn12ORCID,Burdette Joanna E3ORCID,Pavone Mary Ellen1ORCID,Duncan Francesca E1ORCID

Affiliation:

1. Department of Obstetrics and Gynecology, Feinberg School of Medicine, Northwestern University , Chicago, IL, USA

2. Department of Obstetrics and Gynecology, Faculty of Medicine, Chulalongkorn University , Bangkok, Thailand

3. Department of Pharmaceutical Sciences, University of Illinois at Chicago , Chicago, IL, USA

Abstract

Abstract Follicular fluid (FF) is a primary microenvironment of the oocyte within an antral follicle. Although several studies have defined the composition of human FF in normal physiology and determined how it is altered in disease states, the direct impacts of human FF on the oocyte are not well understood. The difficulty of obtaining suitable numbers of human oocytes for research makes addressing such a question challenging. Therefore, we used a heterologous model in which we cultured mouse oocytes in human FF. To determine whether FF has dose-dependent effects on gamete quality, we performed in vitro maturation of denuded oocytes from reproductively young mice (6–12 weeks) in 10%, 50%, or 100% FF from participants of mid-reproductive age (32–36 years). FF impacted meiotic competence in a dose-dependent manner, with concentrations >10% inhibiting meiotic progression and resulting in spindle and chromosome alignment defects. We previously demonstrated that human FF acquires a fibro-inflammatory cytokine signature with age. Thus, to determine whether exposure to an aging FF microenvironment contributes to the age-dependent decrease in gamete quality, we matured denuded oocytes and cumulus–oocyte complexes (COCs) in FF from reproductively young (28–30 years) and old (40–42 years) participants. FF decreased meiotic progression of COCs, but not oocytes, from reproductively young and old (9–12 months) mice in an age-dependent manner. Moreover, FF had modest age-dependent impacts on mitochondrial aggregation in denuded oocytes and cumulus layer expansion dynamics in COCs, which may influence fertilization or early embryo development. Overall, these findings demonstrate that acute human FF exposure can impact select markers of mouse oocyte quality in both dose- and age-dependent manners.

Funder

Department of Obstetrics and Gynecology

Feinberg School of Medicine

Northwestern University

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Cancer Institute

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Obstetrics and Gynecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine

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