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首页> 外文期刊>STEM CELLS >Generation of Parthenogenetic Induced Pluripotent Stem Cells from Parthenogenetic Neural Stem Cells§
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Generation of Parthenogenetic Induced Pluripotent Stem Cells from Parthenogenetic Neural Stem Cells§

机译:从孤雌性神经干细胞生成孤雌性诱导多能干细胞 §

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摘要

Somatic cells can achieve a pluripotent cell state in a process called pluripotential reprogramming. Multipotent stem cells can differentiate into cells of only one lineage, but pluripotent stem cells can give rise to cells of all three germ layers of an organism. In this study, we generated induced pluripotent stem (iPS) cells from bimaternal (uniparental) parthenogenetic neural stem cells (pNSCs) by transduction with either four (4F: Oct4, Klf4, Sox2, and c-Myc) or two (2F: Oct4 and Klf4) transcription factors. The resultant maternal iPS cells, which were reprogrammed directly from pNSCs, were capable of generating germ line-competent chimeras. Interestingly, analysis of global gene expression and imprinting status revealed that parthenogenetic iPS cells clustered closer to parthenogenetic ESCs than to female ESCs, with patterns that were clearly distinct from those of pNSCs. STEM CELLS 2009;27:2962-2968
机译:体细胞可以在称为多能重编程的过程中实现多能细胞状态。多能干细胞可以分化为仅一个谱系的细胞,但是多能干细胞可以产生生物体所有三个胚层的细胞。在这项研究中,我们通过四个(4F:Oct4,Klf4,Sox2和c-Myc)或两个(2F:Oct4)的转导,从双亲(单亲)单性生殖神经​​干细胞(pNSC)生成了诱导多能干(iPS)细胞。和Klf4)转录因子。直接从pNSC重新编程的所得母体iPS细胞能够产生能与生殖系嵌合的嵌合体。有趣的是,对全局基因表达和印迹状态的分析显示,孤雌生殖iPS细胞聚集于孤雌生殖ESC而不是雌性ESC,其模式明显不同于pNSC。干细胞2009; 27:2962-2968

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  • 来源
    《STEM CELLS》 |2009年第12期|2962-2968|共7页
  • 作者单位

    Laboratory of Stem Cell and Developmental Biology, CHA Stem Cell Institute, CHA University, Seoul, Republic of Korea;

    Department of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany;

    Department of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany;

    Department of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany;

    Laboratory of Stem Cell and Developmental Biology, CHA Stem Cell Institute, CHA University, Seoul, Republic of Korea|CHA Bio & Diostech Co., Ltd., Seoul, Republic of Korea;

    Department of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany;

    Department of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany;

    Department of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany;

    CHA Bio & Diostech Co., Ltd., Seoul, Republic of Korea;

    Department of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany;

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