Effect of vitrification on mitochondrial membrane potential in human metaphase II oocytes

被引:46
作者
Chen, Cui [2 ]
Han, Shubiao [1 ]
Liu, Weiwei [1 ]
Wang, Yaping [2 ]
Huang, Guoning [1 ]
机构
[1] Chongqing Obstet & Gynecol Hosp, Chongqing Reprod & Genet Inst, Chongqing 400013, Peoples R China
[2] Chongqing Med Univ, Chongqing 400016, Peoples R China
关键词
Vitrification; Human metaphase II oocyte; Mitochondrial membrane potential; ETHYLENE-GLYCOL; PREIMPLANTATION EMBRYOS; MEIOTIC SPINDLES; HIGH SURVIVAL; CRYOPRESERVATION; MOUSE; EXPERIENCE; FROZEN; PATTERNS; PROTOCOL;
D O I
10.1007/s10815-012-9848-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The aim of this study was to evaluate the impact of vitrification on mitochondrial membrane potential (Delta Im) in human metaphase II (MII) oocytes, and the changes of Delta Im on thawed MII oocytes. MII oocytes were obtained from clinical IVF cycles when the oocytes were failed to fertilization within 24 h after insemination. All oocytes were randomly divided into 4 groups: non-frozen (fresh group), cultured for 0 h (0 h group), 2 h (2 h group) and 4 h (4 h group) after vitrification/thawing. All oocytes were stained with the Delta Im-specific probe JC-1 and detected by laser scanning confocal microscope (LSCM) for mitochondrial analysis. The Delta Im of oocytes was significantly decreased in 0 h and 2 h groups when compared with fresh group (0.93, 1.09 vs 1.34, P < 0.05), but similar between 4 h group and fresh group (1.30 vs 1.34, P > 0.05). In the vitrification/thawing process, the Delta Im of MII oocytes could have temporally dynamic changes within 2 h after thawing but would be fully recovered after 4 h culture.
引用
收藏
页码:1045 / 1050
页数:6
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