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The emergent landscape of the mouse gut endoderm at single-cell resolution

机译:小鼠肠内胚层在单细胞分辨率下的新兴景观

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摘要

Here we delineate the ontogeny of the mammalian endoderm by generating 112,217 single-cell transcriptomes, which represent all endoderm populations within the mouse embryo until midgestation. We use graph-based approaches to model differentiating cells, which provides a spatio-temporal characterization of developmental trajectories and defines the transcriptional architecture that accompanies the emergence of the first (primitive or extra-embryonic) endodermal population and its sister pluripotent (embryonic) epiblast lineage. We uncover a relationship between descendants of these two lineages, in which epiblast cells differentiate into endoderm at two distinct time points-before and during gastrulation. Trajectories of endoderm cells were mapped as they acquired embryonic versus extra-embryonic fates and as they spatially converged within the nascent gut endoderm, which revealed these cells to be globally similar but retain aspects of their lineage history. We observed the regionalized identity of cells along the anterior-posterior axis of the emergent gut tube, which reflects their embryonic or extra-embryonic origin, and the coordinated patterning of these cells into organ-specific territories.
机译:在这里,我们通过生成112,217单细胞转录组来描述哺乳动物内胚层的个体发育,该单细胞转录组代表小鼠胚胎中直至妊娠的所有内胚层群体。我们使用基于图的方法对分化细胞进行建模,该模型提供了发育轨迹的时空特征,并定义了第一个(原始或胚外)内胚层及其姊妹多能(胚)上皮细胞出现时的转录结构血统。我们揭示了这两个世系的后代之间的关系,其中上胚层细胞在两个不同的时间点(在胃胚形成之前和期间)分化为内胚层。内胚层细胞的轨迹在获得胚胎命运和胚外命运时得到定位,并且在新生肠道内胚层中在空间上会聚,这揭示了这些细胞在全球范围内相似,但保留了其谱系历史的某些方面。我们观察到的细胞沿肠壁的前后轴区域化,这反映了它们的胚胎或胚外起源,以及这些细胞进入器官特定区域的协调模式。

著录项

  • 来源
    《Nature》 |2019年第7756期|361-367|共7页
  • 作者单位

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Dev Biol Program, 1275 York Ave, New York, NY 10021 USA;

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Computat & Syst Biol Program, 1275 York Ave, New York, NY 10021 USA;

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Dev Biol Program, 1275 York Ave, New York, NY 10021 USA;

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Computat & Syst Biol Program, 1275 York Ave, New York, NY 10021 USA;

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Dev Biol Program, 1275 York Ave, New York, NY 10021 USA;

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Computat & Syst Biol Program, 1275 York Ave, New York, NY 10021 USA;

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Dev Biol Program, 1275 York Ave, New York, NY 10021 USA;

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Dev Biol Program, 1275 York Ave, New York, NY 10021 USA;

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Flow Cytometry Core Facil, 1275 York Ave, New York, NY 10021 USA;

    10x Genom, Pleasanton, CA USA;

    10x Genom, Pleasanton, CA USA;

    BC Canc, Terry Fox Lab, Vancouver, BC, Canada;

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Dev Biol Program, 1275 York Ave, New York, NY 10021 USA;

    Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Computat & Syst Biol Program, 1275 York Ave, New York, NY 10021 USA;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 04:17:41

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