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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.
Abstract:
Mono-butyl phthalate (MBP), the metabolite of dibutyl phthalate (DBP), is the most abundant phthalate metabolite found in Chinese women. Extracellular vesicles (EVs) are nanoscale lipid bilayer particles produced by extensive kinds of cells, serving a key role in intercellular communication. Extracellular vesicle miRNAs (EV-miRNAs) in follicular fluid (FF) have been evidenced to be associated with female reproductive health. The objective of this study was to investigate the associations of EV-miRNAs expressed profile with DBP exposure in FF of female participants and expose its potential mechanism in impaired oocyte development. Based on participants' FF MBP concentrations and fertilization status, we compared the miRNA expression between the FF-EVs of group A (high DBP exposure and impaired fertilization) and group B (low DBP exposure and normal fertilization). Compared with group B, miR-1246, miR-3679-5p, miR-423-5p, miR-5585-3p, miR-116-5p, miR-172-5p were upregulated, while miR-34b-3p was downregulated in group A. Target genes of the differently expressed miRNAs were predicted, and the functional analysis was performed. Furthermore, we exposed human ovarian granulosa tumor cell line (KGN) to MBP (4ug/L) to isolate the EVs from the culture medium and validated the expression levels of different miRNAs. We found that MBP exposure was significantly associated with increased levels of miR-116-5p (P = 0.01). In addition, we demonstrated that the most different miRNA, miR-116-5p regulated oocyte fertilization by inhibiting FOXO3a. Our findings suggested that EV-miRNAs in the FF might mediate MBP toxicity in oocytes.
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.
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