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[Mouse oocyte maturation in vitro at a low concentration of pyruvate in the culture medium]
Ontogenez
|January 1, 1985
Abstract:
Mouse oocytes isolated from antrum--containing follicles were cultivated for 17-19 hours in the media with different concentrations of pyruvate. Decrease of pyruvate concentration down to 0.03 mM significantly increased the number of oocytes with intact germinal vesicles. However, in 50% of oocytes desintegration of nuclear membrane and condensation of chromosomes occurred even at a concentration of 0.02 mM.
Insights
Lowering pyruvate levels in mouse oocyte culture media improved germinal vesicle integrity. However, excessively low pyruvate concentrations (0.02 mM) led to nuclear membrane breakdown and chromosome condensation.
Area of Science:
- Reproductive Biology
- Developmental Biology
- Cell Biology
Context:
- Mouse oocytes are crucial for studying early embryonic development.
- Oocyte maturation is sensitive to the surrounding metabolic environment.
- Pyruvate is a key metabolite in cellular respiration and oocyte development.
Purpose:
- To investigate the impact of varying pyruvate concentrations on mouse oocyte maturation and germinal vesicle status.
- To determine the optimal pyruvate concentration for maintaining oocyte nuclear integrity during in vitro culture.
Summary:
- Mouse oocytes from antrum-containing follicles were cultured in media with varying pyruvate concentrations (0.03 mM to 0.02 mM).
- Reduced pyruvate concentrations, particularly down to 0.03 mM, significantly enhanced the proportion of oocytes retaining intact germinal vesicles.
- However, a pyruvate concentration of 0.02 mM resulted in nuclear membrane disintegration and chromosome condensation in 50% of oocytes.
Impact:
- Identifies a critical threshold for pyruvate concentration essential for preserving oocyte meiotic arrest.
- Provides valuable insights for optimizing in vitro maturation protocols for improved oocyte quality.
- Contributes to understanding the metabolic regulation of germinal vesicle maintenance in mammalian oocytes.