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作 者:张彧[1,2] 陈利平[1] 梁鸿斌[2] 李娅杰[1] 赵雅琦[1] 阎芃[1] 杨菲[1] 倪和民[1] 郭勇[1]
机构地区:[1]北京农学院动物科学技术学院,北京102206 [2]北京奶牛中心,北京100192
出 处:《中国农学通报》2012年第29期39-43,共5页Chinese Agricultural Science Bulletin
基 金:自然科学基金"IFNτ协调Galectin15对绵羊体外胚胎着床调节机制的研究"(30871836)
摘 要:为了初步建立有效的牛胚胎与子宫内膜细胞的体外共培养体系。本实验分别将体外受精第7天后的胚胎和孤雌激活,与培养7天的胚胎与子宫内膜细胞共培养,在48、72h后分别统计体外受精实验组和孤雌激活实验组的孵化率。实验结果表明:在本实验室培养条件下,在与子宫内膜细胞共培养48h后,体外受精胚胎和孤雌发育胚胎在孵化率上存在显著差异(40±5)%、(25±5)%,(P<0.05);与子宫内膜共培养72h后,孵化率无显著差异(70±8.66)%,(65±5)%,(P>0.05)。本实验证明了在体外环境下,牛体外胚胎与子宫内膜细胞共培养后能够正常孵化,可以初步建立起牛体外胚胎与子宫内膜细胞的体外共培养体系,并为进一步研究该体系对牛体外胚胎培养质量的影响奠定一些基础。In this study,it was initiated to establish an effective way to co-culture the bovine blastocysts and their uterine endometrium cells in vitro.Here,total 7 days in vitro fertilized(IVF) or 7 days parthenogenetic(PA) bovine blastocysts were put into the quadripuntal broad with 42,72 h uterine endometrium cells.The results showed that,after being co-cultured with the uterine endometrium cells for 48 h,the hatching rate of IVF blastocysts was significantly higher than that of PA group(40±5)% vs(25±5)%,P 0.05),but after being co-cultured for 72 h,there was no significant differences of hatching rate between them(70 ± 8.66)% vs(65±5)%,P0.05).In conclusion,these results suggested that,such kind of in vitro co-culture system between those in vitro produced bovine blastocysts and the uterine endometrium cells,be a potential and effective way for further investigating the quality of bovine embryos.
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