首页> 外文期刊>Journal of Animal Science and Biotechnology >Efficient production of chimeric mice from embryonic stem cells injected into 4- to 8-cell and blastocyst embryos
【24h】

Efficient production of chimeric mice from embryonic stem cells injected into 4- to 8-cell and blastocyst embryos

机译:从注入4至8细胞胚泡和胚泡胚的胚胎干细胞高效生产嵌合小鼠

获取原文
       

摘要

Background Production of chimeric mice is a useful tool for the elucidation of gene function. After successful isolation of embryonic stem (ES) cell lines, there are many methods for producing chimeras, including co-culture with the embryos, microinjection of the ES cells into pre-implantation embryos, and use of tetraploid embryos to generate the full ES-derived transgenic mice. Here, we aimed to generate the transgenic ES cell line, compare the production efficiency of chimeric mice and its proportion to yield the male chimeric mice by microinjected ES cells into 4- to 8-cell and blastocysts embryos with the application of Piezo-Micromanipulator (PMM), and trace the fate of the injected ES cells. Results We successfully generated a transgenic ES cell line and proved that this cell line still maintained pluripotency. Although we achieved a satisfactory chimeric mice rate, there was no significant difference in the production of chimeric mice using the two different methods, but the proportion of the male chimeric mice in the 4- to 8-cell group was higher than in the blastocyst group. We also found that there was no tendency for ES cells to aggregate into the inner cell mass using in vitro culture of the chimeric embryos, indicating that they aggregated randomly. Conclusions These results showed that the PMM method is a convenient way to generate chimeric mice and microinjection of ES cells into 4- to 8-cell embryos can increase the chance of yielding male chimeras compared to the blastocyst injection. These results provide useful data in transgenic research mediated by ES cells.
机译:背景技术嵌合小鼠的产生是阐明基因功能的有用工具。成功分离出胚胎干(ES)细胞系后,有许多产生嵌合体的方法,包括与胚胎共培养,将ES细胞显微注射到植入前的胚胎中以及使用四倍体胚胎生成完整的ES-。衍生的转基因小鼠。在这里,我们的目标是生成转基因ES细胞系,比较嵌合小鼠的生产效率及其通过使用Piezo-Micromanipulator将微型胚胎干细胞显微注射到4至8细胞和胚泡胚胎中产生雄性嵌合小鼠的比例( PMM),并追踪注入的ES细胞的命运。结果我们成功地产生了转基因ES细胞系,并证明该细胞系仍保持多能性。尽管我们获得了令人满意的嵌合小鼠比率,但是使用两种不同方法在嵌合小鼠的生产上没有显着差异,但是在4至8细胞组中雄性嵌合小鼠的比例高于胚泡组。 。我们还发现,使用嵌合胚胎的体外培养,ES细胞没有聚集到内部细胞团中的趋势,表明它们是随机聚集的。结论这些结果表明,PMM方法是产生嵌合小鼠的便捷方法,与胚泡注射相比,将ES细胞显微注射到4至8个细胞的胚胎中可以增加产生雄性嵌合体的机会。这些结果为ES细胞介导的转基因研究提供了有用的数据。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号