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Supplementation with glucose in PZM-3 medium improve the in vitro development of porcine transgenic cloned embryos

机译:用PZM-3中葡萄糖补充改善猪转基因克隆胚胎的体外发育

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The efficiency of producing porcine transgenic cloned embryos is still low due to lower developmental competence compared to in vivo-fertilized/cultured embryos. This phenomenon may correlates with poor culture condition. Energy substrate in culture medium play an important role in optimizing culture condition. This study pertain to investigate the effect of replacing pyruvate and lactate with glucose in PZM-3 medium at the rest part culture period on porcine embryonic development after SCNT. Porcine adult fibroblasts cells were transfected with pEGFP-C1 vector. Then transfected cells were used as donor cells for producing re-constructed embryos. Results have shown that supplement of glucose up to 5mM concentration in PZM-3 at the rest part of culture period improved the development of transgenic cloned embryos. Moreover, supplement of glucose(5mM) as energy substrate in PZM-3 at 48h of culture was optimal time. However, with regard to the percentage of EGFP-positive blastocyst, there was no significant difference between treatments. In conclusion, replacing pyruvate and lactate with glucose in PZM-3 medium at the rest part of culture period was beneficial to the development of transgenic cloned embryos and had no effect on transgene expression.
机译:由于体内受精/培​​养的胚胎相比,产生猪转基因克隆胚胎的效率仍然是低的。这种现象可能与培养条件不良。培养基中的能量基质在优化培养条件方面发挥着重要作用。本研究涉及探讨在SCNT后的猪胚胎发育的猪胚胎发育中替代PZM-3培养基中的丙酮酸和乳酸与葡萄糖的血糖。用PEGFP-C1载体转染猪成人成纤维细胞细胞。然后将转染的细胞用作供体细胞,用于生产重建的胚胎。结果表明,在培养周期的静止部分在PZM-3中补充葡萄糖在PZM-3中提高了转基因克隆胚胎的发育。此外,在培养48H的48H处为PZM-3中的能量衬底提供葡萄糖(5mm)的能量底物是最佳时间。然而,关于EGFP阳性胚泡的百分比,治疗之间没有显着差异。总之,在培养期剩余部分的PZM-3培养基中用葡萄糖替代丙酮酸和乳酸乳糖对转基因克隆胚胎的发育有益,对转基因表达没有影响。

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