首页> 外文期刊>Theriogenology >The effect of different zwitterionic buffers and PBS used for out-of-incubator procedures during standard in vitro embryo production on development, morphology and gene expression of bovine embryos
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The effect of different zwitterionic buffers and PBS used for out-of-incubator procedures during standard in vitro embryo production on development, morphology and gene expression of bovine embryos

机译:在标准体外胚胎生产过程中,用于体外培养程序的不同两性离子缓冲液和PBS对牛胚胎发育,形态和基因表达的影响

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The effect of the zwitterionic buffers HEPES, TES and MOPS and of PBS used for out-of-incubator procedures during standard in vitro embryo production on bovine oocytes and embryo development, morphology and on the expression patterns of eight selected genes: Fgf-4, Lama1, Ube2a, Gsta4, Il6, Sod1, Prss11 and Hspb1, was evaluated. All buffers were prepared at a concentration of 10mM in TALP medium, with the exception of PBS. The total time of oocyte/embryo exposure to each buffer was approximately 41min. The cleavage rates and number of embryos that developed to >/=8 cells at day 4 were no different among the buffers tested, however, more blastocysts developed at day 7, 8 and 9 in HEPES and MOPS treatments than in PBS and TES (P<0.05). No difference between buffers in total and apoptotic cell number was found. Except for Hspb1 and Ube2a genes, the levels of expression of the six remaining transcripts were higher in in vivo than in in vitro embryos irrespective of buffer used (P<0.05). In addition, higher expression of Hspb1 and lower expression of Ube2a and Lama1 were observed in PBS and TES than in MOPS and HEPES treatments (P<0.05). Expression of Fgf-4 and Gsta4 in the in vitro embryos was lower in PBS than in the remaining three buffers (P<0.05) and the level of expression of the Il6 gene was not affected by any buffer tested but was lower in in vitro than in in vivo derived embryos. Expression of both Sod1 and Prss11 genes in MOPS were at the level of the in vivo embryos. These results showed that the choice of buffer and short exposure time of approximately 41min, affects mRNA expression of in vitro produced bovine embryos.
机译:两性离子缓冲液HEPES,TES和MOPS以及用于标准体外胚胎生产过程中的孵化器操作的PBS对牛卵母细胞和胚胎发育,形态以及八个选定基因Fgf-4,评估了Lama1,Ube2a,Gsta4,Il6,Sod1,Prss11和Hspb1。除PBS外,所有缓冲液均在TALP培养基中以10mM的浓度制备。卵母细胞/胚胎暴露于每种缓冲液的总时间约为41分钟。在测试的缓冲液中,第4天发育成> / = 8细胞的卵裂速率和胚胎数量没有差异,但是,在HEPES和MOPS处理中,在第7、8和9天比在PBS和TES中发育出更多的胚泡(P <0.05)。在缓冲液总数和凋亡细胞数之间没有发现差异。除Hspb1和Ube2a基因外,与使用的缓冲液无关,体内其余六个转录本的表达水平均高于体外胚胎(P <0.05)。此外,与MOPS和HEPES处理相比,在PBS和TES中观察到Hspb1高表达,而Ube2a和Lama1低表达(P <0.05)。 PBS中Fgf-4和Gsta4在体外胚胎中的表达低于其余三种缓冲液(P <0.05),Il6基因的表达水平不受任何缓冲液的影响,但在体外低于后者。在体内衍生的胚胎中。 Sod1和Prss11基因在MOPS中的表达均处于体内胚胎的水平。这些结果表明缓冲液的选择和约41min的短暴露时间影响体外产生的牛胚胎的mRNA表达。

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