Trichlorfon-induced polyploidy and nondisjunction in mouse oocytes from preantral follicle culture

Fengyun Sun1, Ilse Betzendahl, Kelly Van Wemmel

  • 1Genetechnology/Microbiology, Faculty of Biology, University of Bielefeld, Bielefeld, Germany.

Mutation Research
|December 11, 2007
PubMed

Insights

Trichlorfon (TCF) insecticide exposure during mouse oocyte maturation causes meiotic errors and polyploidy. This organophosphate disrupts both oocyte and follicle cell functions, potentially leading to chromosomally abnormal embryos.

Area of Science:

  • Reproductive Toxicology
  • Developmental Biology
  • Cell Biology

Background:

  • Organophosphate insecticides like Trichlorfon (TCF) are known choline esterase inhibitors.
  • Previous studies indicated TCF induces meiotic nondisjunction and spindle aberrations in isolated mouse oocytes.

Purpose of the Study:

  • To investigate the dose-response effects of TCF on oocyte maturation within preantral follicles.
  • To determine direct and indirect impacts of TCF on both oocytes and surrounding somatic cells.
  • To explore potential synergistic effects of TCF.

Main Methods:

  • Preantral mouse follicle culture was utilized.
  • Oocytes were matured in vitro with TCF exposure at specific concentrations (100 µg/ml and 6 µg/ml).
  • Hormonal stimulation, in vitro ovulation, and assessment of meiotic progression, spindle formation, and progesterone production were performed.

Main Results:

  • High TCF concentration (100 µg/ml) significantly increased first meiotic nondisjunction.
  • Lower TCF concentration (6 µg/ml) disrupted polar body formation and led to polyploidy due to failed cytokinesis.
  • TCF exposure resulted in aberrant second meiotic spindles and reduced progesterone production by somatic cells.

Conclusions:

  • TCF directly impacts oocyte maturation, inducing aneugenicity and spindle defects.
  • TCF indirectly affects folliculogenesis by impairing somatic cell function, evidenced by reduced mucification and progesterone levels.
  • Chronic TCF exposure may increase the risk of chromosomally unbalanced embryos following fertilization.

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