首页> 美国卫生研究院文献>Cellular Reprogramming >Bone Marrow Mesenchymal Stem Cells Are an Attractive Donor Cell Type for Production of Cloned Pigs As Well As Genetically Modified Cloned Pigs by Somatic Cell Nuclear Transfer
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Bone Marrow Mesenchymal Stem Cells Are an Attractive Donor Cell Type for Production of Cloned Pigs As Well As Genetically Modified Cloned Pigs by Somatic Cell Nuclear Transfer

机译:骨髓间充质干细胞是一种有吸引力的供体细胞类型可通过体细胞核移植生产克隆猪以及基因修饰的克隆猪

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摘要

The somatic cell nuclear transfer (SCNT) technique has been widely applied to clone pigs or to produce genetically modified pigs. Currently, this technique relies mainly on using terminally differentiated fibroblasts as donor cells. To improve cloning efficiency, only partially differentiated multipotent mesenchymal stem cells (MSCs), thought to be more easily reprogrammed to a pluripotent state, have been used as nuclear donors in pig SCNT. Although in vitro–cultured embryos cloned from porcine MSCs (MSCs-embryos) were shown to have higher preimplantation developmental ability than cloned embryos reconstructed from fibroblasts (Fs-embryos), the difference in in vivo full-term developmental rate between porcine MSCs-embryos and Fs-embryos has not been investigated so far. In this study, we demonstrated that blastocyst total cell number and full-term survival abilities of MSCs-embryos were significantly higher than those of Fs-embryos cloned from the same donor pig. The enhanced developmental potential of MSCs-embryos may be associated with their nuclear donors' DNA methylation profile, because we found that the methylation level of imprinting genes and repeat sequences differed between MSCs and fibroblasts. In addition, we showed that use of transgenic porcine MSCs generated from transgene plasmid transfection as donor cells for SCNT can produce live transgenic cloned pigs. These results strongly suggest that porcine bone marrow MSCs are a desirable donor cell type for production of cloned pigs and genetically modified cloned pigs via SCNT.
机译:体细胞核移植(SCNT)技术已广泛应用于克隆猪或生产转基因猪。当前,该技术主要依赖于使用终末分化的成纤维细胞作为供体细胞。为了提高克隆效率,只有部分分化的多能间充质干细胞(MSC)被认为是猪SCNT的核供体,被认为更容易重编程为多能状态。尽管从猪MSCs(MSCs-embryos)克隆的体外培养胚胎显示出比从成纤维细胞(Fs-embryos)重建的克隆胚胎更高的植入前发育能力,但猪MSCs-embryos在体内的长期发育率差异迄今为止,尚未对Fs-embryos进行调查。在这项研究中,我们证明了MSCs胚胎的胚泡总细胞数和足月生存能力显着高于从同一供体猪克隆的Fs胚胎。 MSCs胚胎发育潜力的增强可能与其核供体的DNA甲基化谱有关,因为我们发现印迹基因和重复序列的甲基化水平在MSCs和成纤维细胞之间存在差异。此外,我们证明了使用从转基因质粒转染中产生的转基因猪MSC作为SCNT的供体细胞可以产生活的转基因克隆猪。这些结果强烈表明,猪骨髓MSC是通过SCNT生产克隆猪和基因修饰克隆猪的理想供体细胞类型。

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