Diethylstilbestrol (DES)-induced cell cycle delay and meiotic spindle disruption in mouse oocytes during in-vitro

A Can1, O Semiz

  • 1Department of Histology-Embryology, Ankara University School of Medicine, Sihhiye, 06339 Ankara, Turkey.

Insights

Diethylstilbestrol (DES) impairs mouse oocyte maturation by disrupting meiotic spindle organization. This synthetic estrogen causes dose-dependent cell cycle arrest and microtubule damage during meiosis I and II.

Area of Science:

  • Reproductive Biology
  • Developmental Biology
  • Toxicology

Background:

  • Growing evidence links synthetic estrogen diethylstilbestrol (DES) to adverse effects on the female reproductive system.
  • Understanding DES's impact on oocyte quality is crucial for reproductive health research.

Purpose of the Study:

  • To investigate the in vitro effects of DES on mouse oocyte maturation.
  • To analyze the impact of DES on meiotic spindle assembly and chromosome distribution.

Main Methods:

  • Isolated mouse cumulus-oocyte-complexes (COCs) were exposed to varying doses of DES (5-30 micromol/l) in vitro.
  • Experiments tracked oocytes from the germinal vesicle (GV) stage to metaphase II (MII).
  • Confocal laser scanning microscopy was used to visualize alpha-tubulin, chromosomes, and F-actin.

Main Results:

  • DES exposure inhibited cell cycle progression in a dose-dependent manner during meiosis I.
  • High DES doses prevented oocytes from reaching metaphase I, while lower doses reduced progression.
  • DES caused fragmentation or loosening of meiotic spindles during meiosis II, depending on the dose.

Conclusions:

  • Diethylstilbestrol (DES) causes significant, reversible damage to the meiotic spindle microtubule organization in mouse oocytes during maturation.
  • DES acts as a reproductive toxicant by disrupting critical processes of oocyte development.

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