Lu Qun, Chen Zi-jiang, Gao Xuan, Li Yuan, Yan Jun-hao, Ma Shui-ying, Li Mei
Reproductive Medical Center, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, PR China.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Oct;22(5):524-7.
To investigate the sex chromosomes and the expression of insulin-like growth factor-II (IGF-II) on activated human unfertilized oocytes after intracytoplasmic sperm injection(ICSI) with calcium ionophore A23187 and puromycin.
All 95 discarded oocyes that showed no evidence of fertilization at 16-18 h after in vitro maturation and intracytoplasmic sperm injection cycles (IVM-ICSI)/conventional ICSI were exposed to calcium ionophore A23187 (5 micromol/L) for 5 min and then were incubated with puromycin (10 microg/mL) for 4 h. After activation, the oocytes were cultured in vitro for 3-5 days. The sex chromosome analysis was performed by dual color fluorescence in situ hybridization. The expression of IGF-II on the activated embryos, normal embryos, and parthenotes was examined.
The combination of calcium ionophore A23187 with puromycin could activate the unfertilized oocytes 22 h after ICSI. The activated rate, cleavage rate, and quality of activated embryos of the IVM-ICSI group were similar to those of ICSI group, respectively. Sex chromosome analysis indicated that 8 male and 5 female embryos had been derived from two pronucleus and a second polar body. The expression of IGF-II on activated embryos and normal embryos was high and similar, which was much stronger than that of parthenotes.
The combination of calcium ionophore A23187 with puromycin could effectively activate unfertilized oocytes 22 h after ICSI. Moreover, the unfertilized oocytes activated by calcium ionophore A23187 and puromycin had normal sex chromosomes and expression of IGF-II like the normal embryos. These suggest that oocyte activation may be considered as a remedial measure in the presence of total or nearly total fertilization failure in ICSI.
研究钙离子载体A23187和嘌呤霉素对卵胞浆内单精子注射(ICSI)后激活的人未受精卵母细胞性染色体及胰岛素样生长因子-II(IGF-II)表达的影响。
选取95枚在体外成熟和卵胞浆内单精子注射周期(IVM-ICSI)/传统ICSI后16-18小时未显示受精迹象的废弃卵母细胞,用钙离子载体A23187(5微摩尔/升)处理5分钟,然后用嘌呤霉素(10微克/毫升)孵育4小时。激活后,将卵母细胞体外培养3-5天。采用双色荧光原位杂交进行性染色体分析。检测激活胚胎、正常胚胎和孤雌胚中IGF-II的表达。
钙离子载体A23187与嘌呤霉素联合应用可在ICSI后22小时激活未受精卵母细胞。IVM-ICSI组激活胚胎的激活率、卵裂率和质量分别与ICSI组相似。性染色体分析表明,8个雄性和5个雌性胚胎来源于两个原核和第二极体。激活胚胎和正常胚胎中IGF-II的表达较高且相似,远强于孤雌胚。
钙离子载体A23187与嘌呤霉素联合应用可在ICSI后22小时有效激活未受精卵母细胞。此外,经钙离子载体A23187和嘌呤霉素激活的未受精卵母细胞具有与正常胚胎相似的正常性染色体和IGF-II表达。这些表明,在ICSI存在完全或几乎完全受精失败的情况下,卵母细胞激活可被视为一种补救措施。