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Set up of a serum-free culture system for bovine embryos: embryo development and quality before and after transient transfer.

机译:建立用于牛胚胎的无血清培养系统:瞬时转移前后的胚胎发育和质量。

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It is well known that serum in culture medium negatively affects blastocyst quality. The objective of this work was to develop and test a serum-free culture medium which could improve embryo quality, measured by the resistance to freezing, lipid and glutathione content of the resulting blastocysts, as well as the ability of the blastocysts to elongate after transient transfer to recipient cows. In a first experiment we showed that adding a mixture of insulin, transferrin and selenium to serum-free Synthetic Oviduct Fluid medium (SOF-ITS) improved embryo development and quality. In the second experiment, the addition of BSA to SOF-ITS further improved blastocyst development. Moreover, a reduction in lipid content of morulae was observed in SOF-ITS-BSA by comparison with morulae cultured with serum (SOF-FCS). The resistance to freezing measured by hatching rates 24 h post-thawing was also improved for blastocysts with a diameter between 160 and 180 micro m cultured in SOF-ITS-BSA by comparison to those produced with serum. In order to evaluate the redox potential of the embryos, reduced glutathione content (GSH) was evaluated both before and after cryopreservation. A significant decrease in glutathione was observed after freezing, whatever the culture medium, but no difference was observed between culture conditions. Transient transfers were performed and elongated D-13 embryos were recovered. Elongation was more pronounced and the embryonic disk more often visible in embryos cultured in SOF-ITS-BSA than in embryos cultured with FCS. In conclusion, the serum-free system we developed to produce in vitro bovine embryos meets the developmental and qualitative requirements for a large-scale use.
机译:众所周知,培养基中的血清会对胚泡质量产生负面影响。这项工作的目的是开发和测试一种无血清培养基,该培养基可以提高胚胎的质量,方法是通过对所产生的胚泡的抗冻性,脂质和谷胱甘肽含量的测定,以及胚泡在短暂的时间后伸长的能力来衡量转移到接收母牛。在第一个实验中,我们表明将胰岛素,转铁蛋白和硒的混合物添加到无血清的合成输卵管液培养基(SOF-ITS)中可以改善胚胎发育和质量。在第二个实验中,向SOF-ITS中添加BSA进一步改善了胚泡发育。而且,与用血清培养的桑ula(SOF-FCS)相比,在SOF-ITS-BSA中观察到桑ula的脂质含量降低。与用血清产生的囊胚相比,在SOF-ITS-BSA中培养的直径在160至180微米之间的胚泡,通过解冻后24小时的孵化率测得的抗冻性也得到了提高。为了评估胚胎的氧化还原电位,在冷冻保存之前和之后都评估了降低的谷胱甘肽含量(GSH)。冷冻后,无论使用哪种培养基,都可以观察到谷胱甘肽的显着降低,但是在培养条件之间没有发现差异。进行了瞬时转移并回收了伸长的D-13胚胎。与用FCS培养的胚胎相比,在SOF-ITS-BSA培养的胚胎中伸长更为明显,并且胚盘更常见。总之,我们开发的用于生产体外牛胚胎的无血清系统可以满足大规模使用的发展和质量要求。

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