Vitrification preserves chromatin integrity, bioenergy potential and oxidative parameters in mouse embryos

Reprod Biol Endocrinol. 2013 Apr 3:11:27. doi: 10.1186/1477-7827-11-27.

Abstract

Background: The aim of this study was to evaluate the effects of vitrification on morpho-functional parameters (blastomere/chromatin integrity and bioenergy/oxidative potential) of mouse preimplantation embryos.

Methods: In vivo produced mouse (4/16-cell, morulae and blastocyst-stage) embryos were randomly divided into vitrification and control groups. For vitrification, embryos were exposed to a 2-step loading of ethylene glycol and propylene glycol, before being placed in a small nylon loop and submerged into liquid nitrogen. After warming, the cryoprotectants were diluted by a 3-step procedure. Embryo morphology, chromatin integrity and energy/oxidative status were compared between groups.

Results: Vitrification induced low grade blastomere cytofragmentation (P < 0.05) and low chromatin damage only in embryos at the morula stage (P < 0.001). Mitochondrial (mt) distribution pattern was affected by vitrification only in early embryos (P < 0.001). Mitochondrial activity did not change upon vitrification in morula-stage embryos but it was reduced in blastocyst-stage embryos (P < 0.05). Intracellular ROS levels significantly increased in embryos at the morula and blastocyst stages (P < 0.001). Colocalization of active mitochondria and ROS increased only in vitrified blastocysts.

Conclusions: In conclusion, this study elucidates the developmentally-related and mild effects of vitrification on morphology, nuclear and bioenergy/oxidative parameters of mouse embryos and demonstrates that vitrification is a suitable method for preserving predictive parameters of embryo ability to induce a full-term pregnancy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blastocyst / cytology
  • Blastocyst / drug effects
  • Blastocyst / metabolism
  • Chromatin / genetics
  • Chromatin / metabolism*
  • Cryopreservation / methods*
  • Cryoprotective Agents / pharmacology
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / metabolism*
  • Energy Metabolism*
  • Ethylene Glycol / pharmacology
  • Female
  • Male
  • Mice
  • Mitochondria / metabolism
  • Morula / cytology
  • Morula / drug effects
  • Morula / metabolism
  • Oxidation-Reduction
  • Pregnancy
  • Propylene Glycol / pharmacology
  • Reactive Oxygen Species / metabolism
  • Reproducibility of Results
  • Vitrification*

Substances

  • Chromatin
  • Cryoprotective Agents
  • Reactive Oxygen Species
  • Propylene Glycol
  • Ethylene Glycol