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Updated: Aug 17, 2026

Mouse Oocyte Microinjection, Maturation and Ploidy Assessment
Published on: July 23, 2011
Changes in mouse oocyte membrane potential and permeability during meiotic maturation
Abstract:
Mouse oocytes spontaneously undergo meiotic maturation when removed from the ovary and cultured in vitro. This paper describes the changes in cell surface membrane potential from the germinal vesicle (GV) stage (- 46 mV, inside negative), through germinal vesicle breakdown (GVBD) (- 31 mV), to the polar body (PB) stage (- 17 mV). Radioisotope tracer flux experiments established the total exchangeable internal K at the GV stage in 190 mM, the K efflux rate coefficient as 6.7 X 10(-5) sec-1) and the K permeability as 46.7 X 10(-8) cm sec-1. In comparison with previous results with PB stage oocytes, this suggests that the membrane potential depolarization is caused largely by a decrease in K permeability. When GVBD is blocked with 0.11 mM dibutyryl cyclic AMP, the membrane potential does not depolarize. This suggests a linkage between depolarization and GVBD. However, incubation in 80 mM K medium, which depolarizes the oocyte, does not trigger GVBD. It is concluded that membrane depolarization by itself is not sufficient to cause GVBD.
Insights
Mouse oocytes undergo spontaneous meiotic maturation, involving significant changes in cell membrane potential. Reduced potassium permeability is identified as the primary driver of membrane depolarization during this process.
Area of Science:
- Cell Biology
- Reproductive Biology
- Membrane Physiology
Background:
- Mouse oocytes mature spontaneously in vitro, a process involving critical cellular changes.
- Understanding the electrophysiological events during oocyte maturation is crucial for reproductive science.
Purpose of the Study:
- To investigate the changes in cell surface membrane potential during mouse oocyte meiotic maturation.
- To determine the ionic basis of membrane potential changes and their relationship with germinal vesicle breakdown (GVBD).
Main Methods:
- Measurement of cell surface membrane potential at different meiotic stages (GV, GVBD, PB).
- Radioisotope tracer flux experiments to quantify potassium (K) transport parameters.
- Pharmacological manipulation using dibutyryl cyclic AMP to block GVBD.
Main Results:
- Membrane potential depolarized from -46 mV (GV stage) to -17 mV (PB stage).
- Potassium (K) efflux rate coefficient and permeability were determined at the GV stage.
- A decrease in K permeability was linked to membrane depolarization.
- Blocking GVBD with dibutyryl cyclic AMP prevented depolarization, suggesting a linkage.
- Oocyte depolarization via high K+ medium did not induce GVBD.
Conclusions:
- Membrane potential depolarization during mouse oocyte maturation is primarily due to decreased K+ permeability.
- While linked to GVBD, membrane depolarization alone is insufficient to trigger GVBD.
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