OBJECTIVE: To compare the cytogenetic changes in in vitro- and in vivo-matured oocytes after vitrification. DESIGN: In vitro experiments using murine model. SETTING: Animal model study in university laboratory. ANIMAL(S): CD-1 mice. INTERVENTION(S): In vitro maturation and vitrification of oocytes. MAIN OUTCOME MEASURE(S): Post-warming survival, analysis of spindle and chromosome configurations, aneuploidy screening of parthenogenetically activated oocytes, extent of DNA fragmentation, and early embryonic development after IVF. RESULT(S): Eighty percent of germinal vesicle-stage oocytes matured after in vitro maturation and were cryopreserved by vitrification (n = 354). There was no significant difference in the post-warming survival of in vitro- and in vivo-matured oocytes (94.1% vs. 91.8%, respectively). The majority of in vitro- and in vivo-matured oocytes maintained normal meiotic spindle morphology and chromosome alignment (88.2% vs. 86.9%, respectively) after vitrification and the incidence of aneuploidy was not increased (11.5% vs. 9.3%). However, in vitro-matured oocytes showed a higher rate of DNA fragmentation after vitrification compared to in vivo-matured oocytes. After vitrification, the cleavage and blastocyst formation rates of in vitro-matured oocytes were significantly lower than those of in vivo-matured oocytes (37.0% vs. 60.0% and 5.4% vs. 18.9%, respectively). CONCLUSION(S): Vitrification of in vitro-matured mouse oocytes results in high survival rates, normal meiotic spindle and chromosome alignment, and no increased incidence of aneuploidy. A possible cause of the reduced developmental competence of in vitro-matured and vitrified oocytes may be due to DNA fragmentation.
OBJECTIVE: To compare the cytogenetic changes in in vitro- and in vivo-matured oocytes after vitrification. DESIGN: In vitro experiments using murine model. SETTING: Animal model study in university laboratory. ANIMAL(S): CD-1mice. INTERVENTION(S): In vitro maturation and vitrification of oocytes. MAIN OUTCOME MEASURE(S): Post-warming survival, analysis of spindle and chromosome configurations, aneuploidy screening of parthenogenetically activated oocytes, extent of DNA fragmentation, and early embryonic development after IVF. RESULT(S): Eighty percent of germinal vesicle-stage oocytes matured after in vitro maturation and were cryopreserved by vitrification (n = 354). There was no significant difference in the post-warming survival of in vitro- and in vivo-matured oocytes (94.1% vs. 91.8%, respectively). The majority of in vitro- and in vivo-matured oocytes maintained normal meiotic spindle morphology and chromosome alignment (88.2% vs. 86.9%, respectively) after vitrification and the incidence of aneuploidy was not increased (11.5% vs. 9.3%). However, in vitro-matured oocytes showed a higher rate of DNA fragmentation after vitrification compared to in vivo-matured oocytes. After vitrification, the cleavage and blastocyst formation rates of in vitro-matured oocytes were significantly lower than those of in vivo-matured oocytes (37.0% vs. 60.0% and 5.4% vs. 18.9%, respectively). CONCLUSION(S): Vitrification of in vitro-matured mouse oocytes results in high survival rates, normal meiotic spindle and chromosome alignment, and no increased incidence of aneuploidy. A possible cause of the reduced developmental competence of in vitro-matured and vitrified oocytes may be due to DNA fragmentation.
Authors: Jie Yan; Joao Suzuki; Xiaomin Yu; Frederick W K Kan; Jie Qiao; Ri-Cheng Chian Journal: J Assist Reprod Genet Date: 2010-07-17 Impact factor: 3.412
Authors: Jie Yan; Joao Suzuki; Xiao-Min Yu; Jie Qiao; Frederick W K Kan; Ri-Cheng Chian Journal: J Assist Reprod Genet Date: 2011-05-04 Impact factor: 3.412