4.2 Article

Androgens promote the acquisition of maturation competence in bovine oocytes

Journal

JOURNAL OF REPRODUCTION AND DEVELOPMENT
Volume 61, Issue 3, Pages 211-217

Publisher

SOCIETY REPRODUCTION & DEVELOPMENT-SRD
DOI: 10.1262/jrd.2014-161

Keywords

Androgen; Cow; Oocyte growth; Oocyte maturation

Funding

  1. Japan Society for the Promotion of Science KAKENHI [25292192]
  2. Grants-in-Aid for Scientific Research [26292136, 25292192] Funding Source: KAKEN

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Recent studies in mice suggest that androgens are important for normal follicle development. However, there have been few reports concerning the action of androgens in the growth of oocytes from large animals. The purpose of this study was to determine the roles of androgens in bovine oocyte growth in vitro. Oocyte-granulosa cell complexes (OGCs) collected from 0.4-0.7 mm early antral follicles were cultured for 14 days with 17 beta-estradiol (E-2) and a non-aromatizable androgen, dihydrotestosterone (DHT). We also examined the ability of an androgen receptor (AR) inhibitor, hydroxyflutamide, to antagonize the effect of androgens on the oocytes. During growth culture, the OGC structures collapsed in the medium with DHT alone, while in the presence of E-2, the OGC structures were maintained. In the medium with both androgens and E-2, the mean diameter of oocytes was increased from 95 mu m to around 120 mu m, larger than those grown with E-2 alone (115 mu m). Also in the maturation culture, oocytes grown with androgens (A(4) or DHT) and E-2 showed higher percentages of metaphase II oocytes (63% or 69%, respectively) than those grown with E-2 alone (32%). Moreover, these maturation rates were decreased by hydroxyflutamide in a dose-dependent manner. Immunostaining showed that ARs were expressed in oocytes and granulosa cells in early antral follicles, and the nuclei of granulosa cells showed intense AR expression. In conclusion, although E-2 supports the OGC structure, additional androgens promote oocyte growth and their acquisition of meiotic competence via AR during in vitro growth culture.

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