Title of article :
OPS vitrification of mouse immature oocytes before or after meiosis: the effect on cumulus cells maintenance and subsequent development
Author/Authors :
Lun Suo، نويسنده , , Guang-Bin Zhou، نويسنده , , Qinggang Meng، نويسنده , , Chang-Liang Yan، نويسنده , , Zhi-Qiang Fan، نويسنده , , Xue-Ming Zhao، نويسنده , , Xiang-Wei Fu، نويسنده , , Yanping Wang، نويسنده , , Qing-Jing Zhang and Shi-En Zhu، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
7
From page :
71
To page :
77
Abstract :
Cryopreservation can cause cumulus cell damage around the immature oocytes, which may result in poor subsequent development. To evaluate the effect of the meiosis stage on the cumulus cell cryoinjury and determine the suitable stage for cryopreservation in immature oocytes, mouse oocytes at germinal vesicle (GV) and germinal vesicle breakdown (GVBD) stages were vitrified using open pulled straw (OPS) method. Cumulus cells damage was scored immediately after thawing by double-fluorescent staining. The survival rate of the oocytes was evaluated and the subsequent development of oocytes was assessed through in vitro culture (IVC) and in vitro fertilization (IVF) separately. After vitrification, a higher proportion of cumulus cells of GV oocytes were damaged than those of GVBD and untreated control groups. The survival rate of vitrified GVBD oocytes (94.1%) was significantly higher (p < 0.05) than that of GV oocytes (85.4%). Oocytes vitrified at GVBD stage (55.7%) showed similar cleavage rate compared to those atGV stage (49.2%), but significantly higher (p < 0.05) blastocyst rate (40.9% vs. 27.4%). These results demonstrate that oocytes at GVBD stage remain better cumulus membrane integrity and developmental ability during vitrification than those at GV stage, indicating they are more suitable for immature oocytes cryopreservation in mice.
Keywords :
oocyte , Cumulus cells , vitrification , Germinal vesicle , mouse
Journal title :
Zygote
Serial Year :
2009
Journal title :
Zygote
Record number :
660888
Link To Document :
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