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Examination of a modified cell cycle synchronization method and bovine nuclear transfer using synchronized early G1 phase fibroblast cells

机译:使用同步的早期G1期成纤维细胞检查改良的细胞周期同步方法和牛核转移

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Somatic cell nuclear transfer has a low success rate, due to a high incidence of fetal loss and increased perinatal morbidity/mortality. One factor that may affect the successful development of nuclear transfer embryos is the cell cycle stage of the donor cell. In order to establish a cell cycle synchronization method that can consistently produce cloned embryos and offspring, we examined the effects of different combinations of three cell treatments on the recovery rate of mitotic phase cells using bovine fetal fibroblasts. In the first experiment, we examined the recovery rate of mitotic phase cells by a combination of treatment with a metaphase arrestant (1 microM 2-methoxyestradiol), shaking the plate and selecting cells with a diameter of 20 microns. As a result, 99% of mitotic phase cells were recovered by repeating the combined treatment of metaphase arrestant and shaking, and collection of cells with a specific diameter. In the second experiment, nuclear transfer was carried out using early G1 phase cells by choosing pairs of bridged cells derived from mitotic phase cells recovered by the combined treatment of 1 microM 2-methoxyestradiol and shaking, and collection of cells with a diameter of 20 microns. The reconstructed embryos were transferred to recipient heifers to determine post-implantation development. Development of embryos reconstructed from early G1 phase cells from the >/=6 cells stage on Day 3 to the morula-blastocyst stage on Day 6 was 100%. Ten blastocysts constructed from two cell lines were transferred into 10 recipient heifers. Nine of the 10 recipients delivered single live calves. In conclusion, mitotic phase bovine fibroblast cells were easily recovered by the combined treatments of 1 microM 2-methoxyestradiol, shaking, and selecting cells of the appropriate diameter. Furthermore, nuclear transfer using cells in the early G1 phase as donor cells gave a high rate of offspring production.
机译:体细胞核移植的成功率很低,原因是胎儿丢失的发生率很高,围产期的发病率/死亡率增加。可能影响核移植胚胎成功发育的一个因素是供体细胞的细胞周期阶段。为了建立可以始终如一地产生克隆的胚胎和后代的细胞周期同步方法,我们研究了三种细胞处理方法的不同组合对牛胎儿成纤维细胞对有丝分裂期细胞回收率的影响。在第一个实验中,我们通过结合使用中期阻滞剂(1 microM 2-甲氧基雌二醇),摇动平板并选择直径为20微米的细胞,检查了有丝分裂期细胞的回收率。结果,通过重复中期停滞剂和摇动的组合处理并收集具有特定直径的细胞,回收了99%的有丝分裂期细胞。在第二个实验中,使用早期G1期细胞进行核移植,选择成对的有丝分裂期细胞衍生的桥接细胞对,这些细胞是通过联合处理1 microM 2-甲氧基雌二醇和振摇而回收的,并收集直径为20微米的细胞。将重建的胚胎转移至受体小母牛,以确定植入后的发育。从第3天的> / = 6细胞阶段到第6天的桑ula胚-胚泡阶段,从早期G1期细胞重建的胚胎的发育为100%。由两个细胞系构成的十个胚泡被转移到十个受体小母牛中。 10个收件人中有9个交付了活牛。总之,通过联合处理1 microM 2-甲氧基雌二醇,摇晃并选择合适直径的细胞,可以轻松回收有丝分裂期牛成纤维细胞。此外,使用处于G1早期的细胞作为供体细胞进行核移植,可以提高子代的产生率。

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