DBP Exposure Affects Oocyte Fertilization Via Extracellular Vesicles-Derived miR-116-5p in Ovarian Granulosa Cells

Hongmei Liao1, Wenqu Tian1, Wen Yao1

  • 1Reproductive Medicine Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, People's Republic of China.

Insights

Mono-butyl phthalate (MBP) exposure in women is linked to altered extracellular vesicle microRNAs (EV-miRNAs) in follicular fluid, potentially impairing oocyte development and fertilization. MBP specifically increased miR-116-5p, which inhibits FOXO3a, affecting fertilization.

Area of Science:

  • Reproductive toxicology
  • Environmental health
  • Molecular biology

Background:

  • Mono-butyl phthalate (MBP), a dibutyl phthalate metabolite, is prevalent in Chinese women.
  • Extracellular vesicles (EVs) and their microRNAs (EV-miRNAs) in follicular fluid are crucial for female reproduction.
  • Phthalate exposure is a growing concern for reproductive health.

Purpose of the Study:

  • To investigate the association between DBP exposure, EV-miRNA profiles in follicular fluid, and impaired oocyte development.
  • To explore the potential mechanisms by which DBP exposure affects female fertility.
  • To identify specific EV-miRNAs altered by DBP exposure in follicular fluid.

Main Methods:

  • Comparison of miRNA expression in FF-EVs between high (Group A) and low (Group B) DBP-exposed women with differing fertilization statuses.
  • Prediction of target genes and functional analysis of differentially expressed miRNAs.
  • In vitro exposure of KGN cells to MBP to validate miRNA expression changes and investigate mechanisms.

Main Results:

  • Several miRNAs were differentially expressed in FF-EVs between high and low DBP exposure groups.
  • MBP exposure in vitro significantly increased miR-116-5p levels in EVs.
  • miR-116-5p was identified as a key mediator, inhibiting FOXO3a and affecting oocyte fertilization.

Conclusions:

  • EV-miRNAs in follicular fluid may act as mediators of MBP toxicity to oocytes.
  • MBP exposure can disrupt female reproductive health by altering EV-miRNA profiles.
  • miR-116-5p is a potential biomarker and therapeutic target for DBP-induced reproductive impairment.