Effects of sperm insemination on the final meiotic maturation of mouse oocytes arrested at metaphase I after in vitro maturation.
10.5653/cerm.2017.44.1.15
- Author:
Jeong YOON
1
;
Kyoung Mi JUHN
;
San Hyun YOON
;
Yong KO
;
Jin Ho LIM
Author Information
1. Maria Research Center, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
Arrested metaphase I oocyte;
Calcium oscillations;
Fertilization;
In vitro oocyte maturation
- MeSH:
Animals;
Blastocyst;
Calcium Signaling;
Cell Count;
Embryonic Development;
Female;
Fertilization;
In Vitro Oocyte Maturation Techniques;
In Vitro Techniques*;
Insemination*;
Meiosis;
Metaphase*;
Mice*;
Mice, Inbred ICR;
Oocytes*;
Pregnancy;
Spermatozoa*
- From:Clinical and Experimental Reproductive Medicine
2017;44(1):15-21
- CountryRepublic of Korea
- Language:English
-
Abstract:
OBJECTIVE: The aims of this study were to investigate whether fertilization could induce the resumption of meiosis in mouse oocytes arrested at metaphase I (MI) after in vitro maturation (IVM), and to investigate the effect of Ca²⁺ chelator treatment at the time of fertilization on the transition from MI to metaphase II (MII). METHODS: MII-stage and arrested MI-stage mouse oocytes after IVM were fertilized, and then embryonic development was monitored. Blastocysts from each group were transferred into 2.5 days post-coitum pseudo-pregnant ICR mice. MI oocytes after IVM were treated with a Ca²⁺ chelator to investigate the effect of Ca²⁺ oscillations on their maturation. RESULTS: As insemination time increased, the number of oocytes in the MI group that reached the MII stage also increased. The blastocyst rates and total cell numbers in the MII group were significantly higher than in the MI group. No pregnancy occurred in the MI group, but 10 pregnancies were achieved (10 of 12) in the MII group. The proportion of MI oocytes that matured to MII oocytes after fertilization was significantly higher in the non-treated group than in the Ca²⁺ chelator-treated group. CONCLUSION: The findings that a higher proportion of MI-arrested oocytes progressed to MII after fertilization and that the MI-to-MII transition was blocked by Ca2+ chelator treatments before fertilization indicate that the maturation of MI oocytes to MII oocytes is associated with intracellular Ca²⁺ oscillations driven by fertilization.
