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首页> 外文期刊>Cytotechnology >A comparative study on efficiency of adult fibroblasts and amniotic fluid-derived stem cells as donor cells for production of hand-made cloned buffalo (Bubalus bubalis) embryos
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A comparative study on efficiency of adult fibroblasts and amniotic fluid-derived stem cells as donor cells for production of hand-made cloned buffalo (Bubalus bubalis) embryos

机译:成人成纤维细胞和羊水来源干细胞作为供体细胞生产手工克隆水牛(Bubalus bubalis)胚胎的效率比较研究

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摘要

The efficiency of two cell types, namely adult fibroblasts, and amniotic fluid stem (AFS) cells as nuclear donor cells for somatic cell nuclear transfer by hand-made cloning in buffalo (Bubalus bubalis) was compared. The in vitro expanded buffalo adult fibroblast cells showed a typical “S” shape growth curve with a doubling time of 40.8?h and stained positive for vimentin. The in vitro cultured undifferentiated AFS cells showed a doubling time of 33.2?h and stained positive for alkaline phosphatase, these cells were also found positive for undifferentiated embryonic stem cell markers like OCT-4, NANOG and SOX-2, which accentuate their pluripotent property. Further, when AFS cells were exposed to corresponding induction conditions, these cells differentiated into osteogenic, adipogenic and chondrogenic lineages which was confirmed through alizaran, oil red O and alcian blue staining, respectively. Cultured adult fibroblasts and AFS cells of passages 10–15 and 8–12, respectively, were used as nuclear donors. A total of 94 embryos were reconstructed using adult fibroblast as donor cells with cleavage and blastocyst production rate of 62.8?±?1.8 and 19.1?±?1.5, respectively. An overall cleavage and blastocyst formation rate of 71.1?±?1.2 and 29.9?±?2.2 was obtained when 97 embryos were reconstructed using AFS cells as donor cells. There were no significant differences (P?>?0.05) in reconstructed efficiency between the cloned embryos derived from two donor cells, whereas the results showed that there were significant differences (P?
机译:比较了两种细胞类型的效率,即成年成纤维细胞和羊水干(AFS)细胞作为通过手工克隆在水牛(Bubalus bubalis)中进行体细胞核转移的核供体细胞。体外扩增的成年水牛成纤维细胞显示出典型的“ S”形生长曲线,倍增时间为40.8?h,波形蛋白染色为阳性。体外培养的未分化AFS细胞显示出33.2?h的倍增时间,碱性磷酸酶染色呈阳性,这些细胞也被发现为未分化胚胎干细胞标记(如OCT-4,NANOG和SOX-2)阳性,从而增强了它们的多能性。 。此外,当AFS细胞暴露于相应的诱导条件下时,这些细胞分化为成骨,成脂和成软骨谱系,分别通过茜素,油红O和阿尔辛蓝染色证实。将培养的成年成纤维细胞和第10-15代和8-12代的AFS细胞用作核供体。用成年成纤维细胞作为供体细胞共重建了94个胚胎,卵裂和胚泡产生率分别为62.8±1.8和19.1±1.5。当使用AFS细胞作为供体细胞重建97个胚胎时,整体卵裂和胚泡形成率分别为71.1±1.2和29.9±2.2。来自两个供体细胞的克隆胚胎之间的重建效率没有显着差异(P <> 0.05),而结果表明,克隆胚胎之间的卵裂和胚泡率有显着差异(P 0.05)。来自两个供体细胞组。由AFS细胞产生的胚泡的平均总细胞数(172.4±±5.8)明显高于成年成纤维细胞(148.2±±6.1)(P <0.05)。这项研究表明,在水牛手工克隆中,AFS细胞来源的克隆胚胎的体外发育潜力高于成人成纤维细胞来源的克隆胚胎的体外发育潜力。

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