牛卵子密度和培养辅料对体外胚胎裂解率和囊胚发育率的影响

J. Looman, Zowie Rodriguez, Lyric Waugh, John Gibbons
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摘要

优化体外培养系统对于最大限度地提高牛囊胚的发育至关重要。我们进行了四项实验来探索对培养环境的操作,并研究分组培养胚胎的益处。从屠宰场提取的卵巢中抽取蓇葖果,对选定的卵母细胞进行成熟、受精、涡流处理,并随机放入培养组中。实验 1 评估了卵子培养密度对单个或 5 个、10 个、20 个或 50 个胚胎一组培养的胚胎囊胚发育的影响。实验 2 评估了先前重复的条件培养基对当前培养胚胎发育的影响。在实验 3 中,裂解的胚胎在培养 24 小时后分组。最后,在实验 4 中,将分组胚胎置于 10 μl 培养液滴中,以评估高密度/低培养基体积对胚胎发育的影响。通过卡方(Chi-square)分析表明,虽然各培养组(和实验)的胚胎裂解率相似,但一个胚胎培养组的囊胚发育低于其他组(p < 0.05)。当将先前重复的条件培养基添加到原始培养基中时,20 个和 50 个胚胎的原始培养组和条件培养组的囊胚发育情况相似。将裂解胚胎混合培养时,10 个裂解胚胎组的囊胚发育高于 1 个裂解胚胎组(p < 0.05),但两个培养组的囊胚发育与对照组相似。用 10 μl 滴液培养胚胎时,与 2、10、25 和对照组相比,培养 5 个胚胎组的胚囊发育较低。总之,这些数据表明,在各组的培养环境中存在明显的 "辅助效应",这种效应显然发生在胚胎裂解之后、囊胚发育之前。附加细胞对体外培养的直接或间接作用以及这种辅助效应的机制还需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of bovine ova density and culture supplements on cleavage and blastocyst development rates of in vitro embryos
An optimized in vitro culture system is important to maximize bovine blastocyst development. Four experiments were conducted to explore manipulation of culture environments and investigate the benefits of culturing embryos in groups. Follicles were aspirated from abattoir-derived ovaries and selected oocytes were matured, fertilized, vortexed, and randomly placed in culture groups. Experiment 1 evaluated the effects of ova culture density on blastocyst development among embryos cultured individually or in groups of 5, 10, 20, or 50 embryos. Experiment 2 evaluated the effects of conditioned media from previous replicates on embryo development of the current culture. In Experiment 3, cleaved embryos were grouped together after being in culture for 24 hours. Lastly, in Experiment 4, grouped embryos were placed in 10 μl culture drops to evaluate the effect of high density/low media volume on development. Cleavage and blastocyst rates analyzed via Chi-square indicated that although cleavage rates were similar among culture groups (and experiments), blastocyst development was lower (p < 0.05) in 1 embryo culture group compared to other groups. When conditioned culture media from previous replicates were added to original culture media, blastocyst development was similar among original and conditioned culture groups of 20 and 50 embryos. When cleaved embryos were amalgamated and cultured, blastocyst development was higher (p < 0.05) in culture groups of 10 than 1 cleaved embryo groups but similar to controls for both culture groups. When embryos were cultured in 10 μl drops, embryos cultured in groups of 5 had lower development to blastocysts compared to groups of 2, 10, 25, and control. In conclusion, these data indicated an apparent ‘helper effect’ expressed in culture environments of groups, and this effect apparently occurred after cleavage but before blastocyst development. Direct or indirect role(s) that additional cells have on in vitro culture and the mechanism of this helper effect requires further investigation.
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