Mouse embryos generated from frozen-thawed oocytes can successfully survive a second cryopreservation

Hum Reprod. 2004 Mar;19(3):666-9. doi: 10.1093/humrep/deh144. Epub 2004 Jan 29.

Abstract

Background: To determine whether mouse embryos generated from frozen-thawed oocytes can successfully survive a second cryopreservation.

Methods: Immature C57BL6*BALB/c female mice underwent superovulation and the collected oocytes were divided into three groups. Group A oocytes (n = 107) underwent IVF. Group B oocytes (n = 167) underwent IVF and embryos generated were then cryopreserved. Group C oocytes (n = 94) were cryopreserved, thawed and underwent IVF. Two-four-cell stage embryos were re-cryopreserved and thawed. Embryos from all groups were then cultured to the blastocyst stage.

Results: Cleavage rates to the 2-4-cell stage were 78, 71 and 46% for groups A, B and C respectively. Blastulation rates from 2-4 cell-stage embryos were 37/83 (45%), 27/118 (23%) and 8/35 (23%) for groups A, B and C respectively. Development to blastocysts was observed in 37/107 oocytes (35%), 27/167 oocytes (16%) and only 8/94 oocytes (9%) for groups A, B and C respectively.

Conclusion: Oocyte cryopreservation results in reduced fertilization rates. Embryo cryopreservation reduces blastulation rates by half regardless of whether the oocytes were fertilized fresh or frozen-thawed. Nevertheless, embryos generated from cryopreserved oocytes can survive cryopreservation and develop to the blastocyst stage at rates comparable with embryos obtained from fresh oocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blastocyst / physiology
  • Cleavage Stage, Ovum
  • Cryopreservation*
  • Culture Techniques
  • Embryo, Mammalian / physiology*
  • Embryonic and Fetal Development
  • Female
  • Fertilization
  • Fertilization in Vitro
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Oocytes* / physiology