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首页> 外文期刊>Genesis: the journal of genetics and development >Stable Generation of Serum- and Feeder-Free Embryonic Stem Cell-Derived Mice with Full Germline-Competency by Using a GSK3 Specific Inhibitor
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Stable Generation of Serum- and Feeder-Free Embryonic Stem Cell-Derived Mice with Full Germline-Competency by Using a GSK3 Specific Inhibitor

机译:通过使用GSK3特异性抑制剂稳定产生具有完全种系能力的无血清和无饲养员的胚胎干细胞衍生小鼠

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摘要

C57BL/6 (B6)-derived embryonic stem (ES) cells are not widely used to generate knockout mice despite the advantage of a well-defined genetic background because of poor developmental potential. We newly established serum- and feeder-free B6 ES cells with full developmental potential by using leukemia inhibitory factor (LIF) and 6-bromoindirubin-3'-oxime (BIO), a glycogen synthase kinase-3 (GSK3) inhibitor. BIO treatment significantly increased the expression levels of 364 genes including pluripotency markers such as Nanog and KIf family. Unexpectedly, by aggregating or microinjecting those ES cells to each eight-cell-stage diploid embryo, we stably generated germline-competent ES-derived mice. Furthermore, founder mice completely derived from female XO, heterozygous, or homozygous mutant B6 ES cells were directly available for intercross breeding and phenotypic analysis. We hereby propose that serum- and feeder-free B6 ES cells stimulated with LIF plus GSK3 inhibitor are valuable for generating mouse models on B6 background. genesis 47:414-422, 2009.
机译:C57BL / 6(B6)衍生的胚胎干(ES)细胞由于具有较弱的发育潜力而尽管具有明确的遗传背景,但并未广泛用于产生基因敲除小鼠。我们通过使用白血病抑制因子(LIF)和糖原合酶激酶3(GSK3)抑制剂6-溴代靛红3'-肟(BIO),建立了具有完全发育潜力的无血清和无饲养层的B6 ES细胞。 BIO处理显着提高了364个基因的表达水平,其中包括多能性标记(例如Nanog和KIf家族)。出乎意料的是,通过将这些ES细胞聚集或显微注射到每个八细胞阶段的二倍体胚胎中,我们稳定地生成了能胜任ES的种系小鼠。此外,完全源自雌性XO,杂合或纯合突变B6 ES细胞的创始小鼠可直接用于杂交育种和表型分析。我们在此提出,用LIF加GSK3抑制剂刺激的无血清和无饲养层的B6 ES细胞对于在B6背景上生成小鼠模型具有重要意义。创世记47:414-422,2009。

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