首页> 外文期刊>Theriogenology >An alternative simple method for mass production of chimeric embryos by coculturing denuded embryos and embryonic stem cells in Eppendorf vials
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An alternative simple method for mass production of chimeric embryos by coculturing denuded embryos and embryonic stem cells in Eppendorf vials

机译:通过在Eppendorf小瓶中共培养裸露的胚胎和胚胎干细胞来批量生产嵌合胚胎的另一种简单方法

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The generation of germline competent chimeric mice via embryonic stem (ES) cells is a crucial step in developing gene-manipulated mouse models. To date, techniques for generating chimeric mice include direct microinjection of ES cells into the cavity of 3.5-d post-coitum (dpc) blastocysts and aggregating or coculturing 2.5 dpc zona pellucida-free (denuded) embryos with ES cells. We present here a procedure that is simple and reproducible for mass producing (10-150 embryos/vial/time) chimeric embryos by coculturing denuded 8-cell embryos and morula in 0.8 mL KSOM-AA medium containing 5 x 10(5)mL-1 purified green fluorescence protein-expressing ES cells (either fresh or thawed) in an 1.7 mL Eppendorf vial for 3h. The resulting chimeras had substantial levels of chimerism and high germline transmission rates. Therefore, the method developed in this study can provide a simple and mass reproducible alternative method (to germline transmitter chimeric mice), without technological and instrumental difficulties, for generating chimeric embryos.
机译:通过胚胎干(ES)细胞生成能产生生殖功能的嵌合小鼠是开发基因操纵的小鼠模型的关键步骤。迄今为止,用于产生嵌合小鼠的技术包括将ES细胞直接显微注射到3.5天后的coitum(dpc)胚泡腔中,以及将2.5 dpc无透明带(裸露)的胚胎与ES细胞聚集或共同培养。我们在这里介绍一种简单的方法,可通过在8 mL含有5 x 10(5)mL-的KSOM-AA培养基中共培养裸露的8细胞胚胎和桑ula来大量生产(10-150个胚胎/小瓶/时间)嵌合胚胎。在1.7 mL Eppendorf小瓶中将1个纯化的表达绿色荧光蛋白的ES细胞(新鲜或解冻)放置3h。产生的嵌合体具有大量的嵌合体和高的种系传递速率。因此,在这项研究中开发的方法可以提供一种简单且可大规模重现的替代方法(对于种系递质嵌合小鼠),而无需技术和仪器方面的困难,即可产生嵌合胚胎。

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