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.

PubMed
Abstract

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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