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首页> 外文期刊>Transgenic Research >Production of mouse chimeras by injection of embryonic stem cells into the perivitelline space of one-cell stage embryos
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Production of mouse chimeras by injection of embryonic stem cells into the perivitelline space of one-cell stage embryos

机译:通过将胚胎干细胞注入单细胞期胚胎的周玻璃体空间来产生小鼠嵌合体

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Generation of mouse chimeras is useful for the elucidation of gene function. In the present report, we describe a new technique for the production of chimeras by injection of R1 embryonic stem (ES) cells into the perivitelline space of one-cell stage mouse embryos. One-cell embryos are injected with 2–6 ES cells into the perivitelline space under the zona pellucida without laser-assistance. Our embryo culture experiments reveal that ES cells injected at the one-cell stage embryo start to be incorporated into the blastomeres beginning at the 8-cell stage and form a chimeric blastocyst after 4 days. We have used this approach to successfully produce a high rate of mouse chimeras in two different mouse genetic backgrounds permitting the establishment of germ line transmitters. This method allows for the earlier introduction of ES cells into mouse embryos, and should free up the possibility of using frozen one-cell embryos for this purpose.
机译:小鼠嵌合体的产生可用于阐明基因功能。在本报告中,我们描述了一种通过将R1胚胎干(ES)细胞注射到单细胞阶段小鼠胚胎的周玻璃体空间中来产生嵌合体的新技术。在没有激光辅助的情况下,将具有2–6个ES细胞的单细胞胚胎注射到透明带下的周玻璃体腔中。我们的胚胎培养实验表明,在单细胞阶段胚胎中注入的ES细胞从8细胞阶段开始就开始并入卵裂球,并在4天后形成嵌合胚泡。我们已经使用这种方法在两个不同的小鼠遗传背景中成功产生了高比例的小鼠嵌合体,从而允许建立种系递质。这种方法可以将ES细胞更早地引入小鼠胚胎,并应释放为此目的使用冷冻单细胞胚胎的可能性。

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