首页> 外文期刊>The Journal of Reproduction and Development >Effect of embryo density on in vitro development and gene expression in bovine in vitro-fertilized embryos cultured in a microwell system.
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Effect of embryo density on in vitro development and gene expression in bovine in vitro-fertilized embryos cultured in a microwell system.

机译:胚胎密度对在微孔系统中培养的牛体外受精胚胎的体外发育和基因表达的影响。

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To identify embryos individually during in vitro development, we previously developed the well-of-the-well (WOW) dish, which contains 25 microwells. Here we investigated the effect of embryo density (the number of embryos per volume of medium) on in vitro development and gene expression of bovine in vitro-fertilized embryos cultured in WOW dishes. Using both conventional droplet and WOW culture formats, 5, 15, and 25 bovine embryos were cultured in 125 micro l medium for 168 h. The blastocysts at Day 7 were analyzed for number of cells and expression of ten genes (CDX2, IFN-tau, PLAC8, NANOG, OCT4, SOX2, AKR1B1, ATP5A1, GLUT1 and IGF2R). In droplet culture, the rates of formation of >4-cell cleavage embryos and blastocysts were significantly lower in embryos cultured at 5 embryos per droplet than in those cultured at 15 or 25 embryos per droplet, but not in WOW culture. In both droplet and WOW culture, developmental kinetics and blastocyst cell numbers did not differ among any groups. IFN-tau expression in embryos cultured at 25 embryos per droplet was significantly higher than in those cultured at 15 embryos per droplet and in artificial insemination (AI)-derived blastocysts. Moreover, IGF2R expression was significantly lower in the 25-embryo group than in the 5-embryo group and in AI-derived blastocysts. In WOW culture, these expressions were not affected by embryo density and were similar to those in AI-derived blastocysts. These results suggest that, as compared with conventional droplet culture, in vitro development and expression of IFN-tau and IGF2R in the microwell system may be insensitive to embryo density.
机译:为了在体外发育过程中单独鉴定胚胎,我们之前开发了“ WOW”培养皿(WOW),该培养皿包含25个微孔。在这里,我们研究了胚胎密度(每体积培养基中的胚胎数)对在WOW皿中培养的牛体外受精胚胎的体外发育和基因表达的影响。使用常规的液滴和WOW培养形式,将5、15和25个牛胚胎在125微升培养基中培养168小时。分析第7天的胚泡的细胞数和十个基因(CDX2,IFN-τ,PLAC8,NANOG,OCT4,SOX2,AKR1B1,ATP5A1,GLUT1和IGF2R)的表达。在小滴培养中,以每滴5个胚胎培养的胚胎中,> 4细胞分裂胚胎和胚泡的形成速率显着低于每滴以15或25个胚胎培养的胚胎,但在WOW培养中则没有。在小滴培养和WOW培养中,任何一组的发育动力学和囊胚细胞数量均无差异。以每滴25个胚胎培养的胚胎中IFN-tau表达明显高于以每滴15个胚胎培养的胚胎和人工授精(AI)衍生的胚泡中的IFN-tau表达。此外,IGF2R表达在25胚胎组明显低于5胚胎组和AI衍生的胚泡。在WOW培养中,这些表达不受胚胎密度的影响,与AI衍生的胚泡中的表达相似。这些结果表明,与常规液滴培养相比,微孔系统中IFN-tau和IGF2R的体外发育和表达可能对胚胎密度不敏感。

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