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Updated: Jun 10, 2025

Mouse Oocyte Microinjection, Maturation and Ploidy Assessment
Published on: July 23, 2011
Sperm penetration at the maturing metaphase I stage can trigger oocyte activation in a mouse model
Ching-Chien Chang1, Min Peng2, Li-Kuang Tsai2
1Reproductive Biology Associates, Atlanta, GA, USA.
Research Question:
Can spermatozoa penetrate maturing metaphase I (MI) oocytes, and render subsequent development following conventional IVF in a mouse model?
Design:
ICR mice were used in this study. Metaphase II (MII) cumulus-oocyte complexes (COC) harvested 15 h after injection of human chorionic gonadotrophin (HCG) were used for IVF as the control group (Group 1). In the treatment group (Group 2), maturing MI COC harvested 7 h after HCG injection were used for IVF. Fertilization, pronuclear formation, cleavage, blastocyst formation, DNA methylation status, chromosome number and live birth rates were used to evaluate the developmental dynamics and competency of maturing MI oocytes following conventional IVF.
Results:
Maturing MI COC were fertilized using conventional IVF, and sperm penetration at MI-telophase I triggered oocyte activation. Most embryos resulting from fertilized MI oocytes developed to blastocyst stage during preimplantation development, albeit a substantial proportion of them were triploids due to the absence of the second meiotic division. Some of the embryos derived from fertilization of maturing oocytes were able to implant and gave rise to full-term development.
Conclusion:
Maturing MI COC from follicles before ovulation could be used for mouse IVF, and fertilized MI oocytes had high potential for development. Healthy offspring can be generated from maturing MI COC following conventional IVF. MI COC may represent a valuable source of 'usable' biomaterial in assisted reproduction. However, many embryos derived from MI COC via IVF have abnormal chromosome numbers in the mouse model. The implications of these findings for human IVF remain to be investigated.
Insights
Fertilizing maturing metaphase I oocytes in mice via IVF can lead to healthy offspring, though abnormal chromosome numbers are a concern. This suggests maturing oocytes are a potential source of biomaterial for assisted reproduction.
Area of Science:
- Reproductive Biology
- Developmental Biology
- Assisted Reproductive Technology
Background:
- Conventional in vitro fertilization (IVF) typically uses metaphase II (MII) oocytes.
- The developmental potential of maturing metaphase I (MI) oocytes following IVF is less understood.
- Investigating alternative oocyte sources could expand options in assisted reproduction.
Purpose of the Study:
- To determine if spermatozoa can penetrate maturing MI oocytes.
- To evaluate the subsequent development of oocytes fertilized at the MI stage using conventional IVF.
- To assess the viability and chromosomal integrity of embryos derived from MI oocytes.
Main Methods:
- ICR mice were utilized for oocyte collection at different time points post-HCG injection.
- Maturing MI oocytes (7h post-HCG) and MII oocytes (15h post-HCG) were subjected to conventional IVF.
- Developmental parameters including fertilization, cleavage, blastocyst formation, and live birth rates were assessed.
- Chromosomal number and DNA methylation status were analyzed.
Main Results:
- Spermatozoa successfully penetrated maturing MI oocytes, triggering activation.
- A significant proportion of embryos from fertilized MI oocytes reached the blastocyst stage.
- Despite developmental potential, a substantial number of these embryos were triploid due to the absence of the second meiotic division.
- Live births were achieved from some embryos derived from MI oocytes.
Conclusions:
- Maturing MI oocytes can be fertilized via conventional IVF and possess developmental potential.
- Healthy offspring can be produced from maturing MI oocytes, indicating their potential as a biomaterial source in assisted reproduction.
- The high incidence of aneuploidy in embryos derived from MI oocytes warrants further investigation, particularly regarding implications for human IVF.
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