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A developmental coordinate of pluripotency among mice, monkeys and humans

机译:小鼠,猴子和人类之间多能性的发育坐标

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摘要

The epiblast (EPI) is the origin of all somatic and germ cells in mammals, and of pluripotent stem cells in vitro. To explore the ontogeny of human and primate pluripotency, here we perform comprehensive single-cell RNA sequencing for pre and post-implantation EPI development in cynomolgus monkeys (Macacafascicularis). We show that after specification in the blastocysts, EPI from cynomolgus monkeys (cyEPI) undergoes major transcriptome changes on implantation. Thereafter, while generating gastrulating cells, cyEPI stably maintains its transcriptome over a week, retains a unique set of pluripotency genes and acquires properties for 'neuron differentiation'. Human and monkey pluripotent stem cells show the highest similarity to post-implantation late cyEPI, which, despite co-existing with gastrulating cells, bears characteristics of pre-gastrulating mouse EPI and epiblast-like cells in vitro. These findings not only reveal the divergence and coherence of EPI development, but also identify a developmental coordinate of the spectrum of pluripotency among key species, providing a basis for better regulation of human pluripotency in vitro.
机译:表皮细胞(EPI)是哺乳动物中所有体细胞和生殖细胞以及体外多能干细胞的起源。为了探索人类和灵长类动物多能性的个体发育,我们在猕猴(Macacafascicularis)的植入前和植入后EPI发育中进行了全面的单细胞RNA测序。我们表明,在囊胚规格后,食蟹猴的EPI(cyEPI)在植入时经历了主要的转录组变化。此后,cyEPI在产生胃动细胞的同时,稳定地维持其转录组超过一周,保留了一组独特的多能性基因,并获得了“神经元分化”的特性。人和猴多能干细胞与植入后的cyEPI具有最高的相似性,尽管它们与胃泌素细胞共存,但在体外具有预妊娠小鼠EPI和上皮样细胞的特征。这些发现不仅揭示了EPI发展的差异性和连贯性,而且还确定了关键物种之间多能性谱的发展坐标,为更好地调节人的多能性提供了基础。

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  • 来源
    《Nature》 |2016年第7618期|57-62|共6页
  • 作者单位

    Kyoto Univ, Grad Sch Med, Dept Anat & Cell Biol, Sakyo Ku, Yoshida Konoe Cho, Kyoto 6068501, Japan|JST, ERATO, Sakyo Ku, Yoshida Konoe Cho, Kyoto 6068501, Japan;

    Kyoto Univ, Grad Sch Med, Dept Anat & Cell Biol, Sakyo Ku, Yoshida Konoe Cho, Kyoto 6068501, Japan|JST, ERATO, Sakyo Ku, Yoshida Konoe Cho, Kyoto 6068501, Japan;

    Kyoto Univ, Grad Sch Med, Dept Anat & Cell Biol, Sakyo Ku, Yoshida Konoe Cho, Kyoto 6068501, Japan|JST, ERATO, Sakyo Ku, Yoshida Konoe Cho, Kyoto 6068501, Japan;

    Kyoto Univ, Grad Sch Med, Dept Anat & Cell Biol, Sakyo Ku, Yoshida Konoe Cho, Kyoto 6068501, Japan|JST, ERATO, Sakyo Ku, Yoshida Konoe Cho, Kyoto 6068501, Japan;

    Shiga Univ Med Sci, Res Ctr Anim Life Sci, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan;

    Shiga Univ Med Sci, Res Ctr Anim Life Sci, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan;

    Shiga Univ Med Sci, Res Ctr Anim Life Sci, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan;

    Shiga Univ Med Sci, Res Ctr Anim Life Sci, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan;

    Kyoto Univ, Ctr iPS Cell Res & Applicat, Sakyo Ku, 53 Kawahara Cho, Kyoto 6068507, Japan|Kyoto Univ, Inst Integrated Cell Material Sci, Sakyo Ku, Yoshida Ushinomiya Cho, Kyoto 6068501, Japan|AMED, CREST, Chiyoda Ku, 1-7-1 Otemachi, Tokyo 1000004, Japan;

    Kyoto Univ, Grad Sch Med, Dept Anat & Cell Biol, Sakyo Ku, Yoshida Konoe Cho, Kyoto 6068501, Japan|JST, ERATO, Sakyo Ku, Yoshida Konoe Cho, Kyoto 6068501, Japan|Kyoto Univ, Ctr iPS Cell Res & Applicat, Sakyo Ku, 53 Kawahara Cho, Kyoto 6068507, Japan|Kyoto Univ, Inst Integrated Cell Material Sci, Sakyo Ku, Yoshida Ushinomiya Cho, Kyoto 6068501, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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