Epigenetic effects of bisphenol a on granulosa cells of mouse follicles during in vitro culture: An experimental study

3Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

Abstract

Background: Bisphenol A (BPA), a synthetic endocrine-disrupting chemical, is reproductive toxicant. Granulosa cells have significant roles in follicle developmentand KIT ligand (KITL) and Anti-Müllerian hormone (AMH) are essential biomoleculeproduced by them during folliculogenesis. Objective: Due to the widespread use of BPA and its potential epigenetic effects, thistudy examined the impact of BPA on promoter methylation of amh and kitl genes in mouse granulosa cells. Materials and Methods: Preantral follicles were isolated from ovaries of immature mice and cultured for eight days. Then, follicles were treated with 50 and 100 μM of BPA, and 0.01% (v/v) ethanol for 24 and 72 hr. Growth and degeneration of follicles and antrum formation were analyzed. The granulosa cells were isolated mechanically, and theiextracted DNA was treated with sodium bisulfite. The promoter regions of the amh and kitl were analyzed with PCR and sequencing. Results: BPA did not change follicle survival and antrum formation significantly (p 0.41). However, the culture in the presence of 100 μM BPA had an inhibitory effecon growth. Before BPA treatment, the CpG of the kitl and amh promoters were unmethylated and partially methylated, respectively. While the percent of 5mC in the amh promoter reduced at 100 μM of BPA, it did not alter the kitl promoter methylationConclusion: BPA at higher concentrations has an inhibitory effect on follicle growthMoreover, it seems that the epigenetic impact of BPA restricts to the demethylation oCpG sites.

Cite

CITATION STYLE

APA

Khaghani, A. J., Farrokh, P., & Zavareh, S. (2021). Epigenetic effects of bisphenol a on granulosa cells of mouse follicles during in vitro culture: An experimental study. International Journal of Reproductive BioMedicine, 19(2), 129–136. https://doi.org/10.18502/ijrm.v19i2.8471

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free