首页 | 本学科首页   官方微博 | 高级检索  
     检索      

不同激活方法对小鼠卵母细胞孤雌发育及二倍体形成的影响
引用本文:赵天闯,张鹏,陈玥,高飞,唐博,李子义.不同激活方法对小鼠卵母细胞孤雌发育及二倍体形成的影响[J].中国兽医学报,2011,31(8).
作者姓名:赵天闯  张鹏  陈玥  高飞  唐博  李子义
作者单位:吉林大学畜牧兽医学院动物胚胎工程吉林省重点实验室,吉林长春,130062
基金项目:国家自然科学基金资助项目(30901056); 博士点新教师基金资助项目(20090061120010)
摘    要:卵母细胞的孤雌激活是研究哺乳动物受精机制和发育机理的有效方法,也是细胞核移植、显微注射受精技术、孤雌胚胎干细胞等研究内容中的重要环节。本试验分别用乙醇、SrCl2、钙离子载体A23187对小鼠卵母细胞进行单独孤雌激活,并分别与6-DMAP联合运用,对小鼠卵母细胞进行联合孤雌激活。结果显示:(1)不同激活剂单独或联合激活,对卵母细胞的激活率有显著影响(P〈0.05),SrCl2组的激活率最高(92%~94%);(2)相同激活剂对卵母细胞孤雌囊胚的发育率在单独激活组(SrCl2组,18%)和联合激活组(SrCl2+6-DMA组,53%)中存在显著差异(P〈0.05);(3)相同激活剂对卵母细胞二倍体率在单独激活组(钙离子载体A23187组,21%)和联合激活组(钙离子载体A23187+6-DMA组,77%)中均存在显著差异(P〈0.05)。结果表明:(1)SrCl2可以对小鼠卵母细胞进行有效的孤雌激活;(2)联合激活法可以显著提高孤雌卵母细胞的囊胚发育率;3、6-DMAP可以抑制第二极体排出,显著提高孤雌激活卵母细胞的二倍体率。

关 键 词:孤雌激活  二倍体  小鼠

Effects of different activation methods on parthenogenetic development and diploid formation of mouse oocytes
ZHAO Tian-chuang,ZHANG Peng,CHEN Yue,GAO Fei,TANG Bo,LI Zi-yi.Effects of different activation methods on parthenogenetic development and diploid formation of mouse oocytes[J].Chinese Journal of Veterinary Science,2011,31(8).
Authors:ZHAO Tian-chuang  ZHANG Peng  CHEN Yue  GAO Fei  TANG Bo  LI Zi-yi
Institution:ZHAO Tian-chuang,ZHANG Peng,CHEN Yue,GAO Fei,TANG Bo,LI Zi-yi(Jilin Provincial Key Laboratory of Animal Embryo Engineering,College of Animal Science and Veterinary Medicine,Jilin University,Changchun 130062,China)
Abstract:Parthenogenetic oocyte activation is an effective method for studies of mechanisms of mammalian fertilization and development,and an important part for studies of nuclear transfer,microinjection fertilization techniques,parthenogenetic embryonic stem cell research as well.Effects of ethanol,SrCl2 and Ca-A23187 on parthenogenetic activation rate and diploid rate of mouse oocytes,either individually or in combination with the use of 6-DMAP were investigated in this study.Our results showed:activation rates of...
Keywords:parthenogenesis  diploid  mice  
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号