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Updated: Aug 18, 2026

Meiotic Spindle Assessment in Mouse Oocytes by siRNA-mediated Silencing
Published on: October 11, 2015
Diethylstilbestrol (DES)-induced cell cycle delay and meiotic spindle disruption in mouse oocytes during in-vitro
1Department of Histology-Embryology, Ankara University School of Medicine, Sihhiye, 06339 Ankara, Turkey.
Abstract:
Due to the growing amount of data related to the deleterious effects of the synthetic oestrogenic compound, diethylstilbestrol (DES), on the female reproductive system, we tested the potential effects of this compound on mouse oocytes. Controlled time- and dose-dependent in-vitro experiments were carried out on isolated cumulus-oocyte-complexes (COCs) to examine the meiotic spindle assembly and chromosome distribution. alpha-tubulin, chromosomes and F-actin were labelled and detected by confocal laser scanning microscope. COCs were exposed to varying doses of DES (5-30 micromol/l) from the germinal vesicle (GV) stage to the end of metaphase II (MII) when meiosis I and meiosis II is normally completed. Exposure to DES during meiosis I caused a dose-dependent inhibition of cell cycle progression. In comparison with controls, fewer oocytes reached metaphase I (MI) at low doses (5 micromol/l) of DES, while none of the oocytes reached MI in high doses (30 micromol/l). When COCs were exposed to high doses of DES during meiosis II, fragmentation of first meiotic spindle was detected, whereas lower doses caused loosening of the first and the second meiotic spindles. No microtubular abnormalities were detected either in GV-stage oocytes or in cumulus cells. The above data demonstrate that one mode of action of DES on mouse oocytes is a severe yet reversible deterioration of meiotic spindle microtubule organization during maturation.
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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