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首页> 外文期刊>Transgenic research >Comparison of male chimeric mice generated from microinjection of JM8.N4 embryonic stem cells into C57BL/6J and C57BL/6NTac blastocysts
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Comparison of male chimeric mice generated from microinjection of JM8.N4 embryonic stem cells into C57BL/6J and C57BL/6NTac blastocysts

机译:将JM8.N4胚胎干细胞显微注射到C57BL / 6J和C57BL / 6NTac胚泡中产生的雄性嵌合小鼠的比较

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摘要

To identify ways to improve the efficiency of generating chimeric mice via microinjection of blastocysts with ES cells, we compared production and performance of ES-cell derived chimeric mice using blastocysts from two closely related and commonly used sub-strains of C57BL/6. Chimeras were produced by injection of the same JM8.N4 (C57BL/6NTac) derived ES cell line into blastocysts of mixed sex from either C57BL/6J (B6J) or C57BL/6NTac (B6NTac) mice. Similar efficiency of production and sex-conversion of chimeric animals was observed with each strain of blastocyst. However, B6J chimeric males had fewer developmental abnormalities involving urogenital and reproductive tissues (1/12, 8 %) compared with B6NTac chimeric males (7/9, 78 %). The low sample size did not permit determination of statistical significance for many parameters. However, in each category analyzed the B6J-derived chimeric males performed as well, or better, than their B6NTac counterparts. Twelve of 14 (86 %) B6J male chimeras were fertile compared with 6 of 11 (55 %) B6NTac male chimeras. Ten of 12 (83 %) B6J chimeric males sired more than 1 litter compared with only 3 of 6 (50 %) B6NTac chimeras. B6J male chimeras produced more litters per productive mating (3.42 ± 1.73, n = 12) compared to B6NTac chimeras (2.17 ± 1.33, n = 6). Finally, a greater ratio of germline transmitting chimeric males was obtained using B6J blastocysts (9/14; 64 %) compared with chimeras produced using B6NTac blastocysts (4/11; 36 %). Use of B6J host blastocysts for microinjection of ES cells may offer improvements over blastocysts from B6NTac and possibly other sub-strains of C57BL/6 mice.
机译:为了确定通过将胚泡与ES细胞一起显微注射来提高产生嵌合小鼠的效率的方法,我们比较了使用来自两个紧密相关且常用的C57BL / 6亚株的胚泡的ES细胞衍生嵌合小鼠的生产和性能。通过将相同的JM8.N4(C57BL / 6NTac)衍生的ES细胞系注射到来自C57BL / 6J(B6J)或C57BL / 6NTac(B6NTac)小鼠的混合性胚泡中来产生嵌合体。每种囊胚菌株都观察到了相似的嵌合动物生产和性别转化效率。但是,与B6NTac嵌合雄性(7 / 9,78%)相比,B6J嵌合雄性涉及泌尿生殖系统和生殖组织的发育异常较少(1 / 12,8%)。低样本量无法确定许多参数的统计显着性。但是,在每个类别中,B6J衍生的嵌合雄性动物的表现均优于或优于B6NTac。 14个B6J雄性嵌合体中有12个(86%)能繁殖,而11个B5NTac雄性嵌合体中有6个(55%)可育。 12个B6J嵌合雄性中有10个(1个)产仔数多,而6个B6NTac嵌合体中只有3个(50%)。与B6NTac嵌合体(2.17±1.33,n = 6)相比,B6J雄性嵌合体在每次生产交配时产仔数更多(3.42±1.73,n = 12)。最后,与使用B6NTac胚泡产生的嵌合体(4/11; 36%)相比,使用B6J胚泡获得的生殖系传递嵌合雄性比例更高(9/14; 64%)。使用B6J宿主囊胚进行ES细胞显微注射可能比B6NTac和C57BL / 6小鼠其他亚株的囊胚有所改善。

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