Spatial transcriptomic characterization of a Carnegie stage 7 human embryo

IF 17.3 1区 生物学 Q1 CELL BIOLOGY
Lina Cui, Sirui Lin, Xiaolong Yang, Xinwei Xie, Xiaoyan Wang, Nannan He, Jingyu Yang, Xin Zhang, Xiaojian Lu, Xiaodi Yan, Yifei Guo, Bailing Zhang, Ran Li, Hefan Miao, Mei Ji, Runzhao Zhang, Leqian Yu, Zhenyu Xiao, Yulei Wei, Jingtao Guo
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Abstract

Gastrulation marks a pivotal stage in mammalian embryonic development, establishing the three germ layers and body axis through lineage diversification and morphogenetic movements. However, studying human gastrulating embryos is challenging due to limited access to early tissues. Here we show the use of spatial transcriptomics to analyse a fully intact Carnegie stage 7 human embryo at single-cell resolution, along with immunofluorescence validations in a second embryo. Employing 82 serial cryosections and Stereo-seq technology, we reconstructed a three-dimensional model of the embryo. Our findings reveal early specification of distinct mesoderm subtypes and the presence of the anterior visceral endoderm. Notably, primordial germ cells were located in the connecting stalk, and haematopoietic stem cell-independent haematopoiesis was observed in the yolk sac. This study advances our understanding of human gastrulation and provides a valuable dataset for future research in early human development. Guo and colleagues characterize an intact Carnegie stage 7 human embryo at single-cell resolution in a spatially resolved manner.

Abstract Image

Abstract Image

卡内基7期人类胚胎的空间转录组学特征
原肠胚形成标志着哺乳动物胚胎发育的关键阶段,通过谱系多样化和形态发生运动建立了三个胚层和体轴。然而,由于获取早期组织的途径有限,研究人类原肠泌胚具有挑战性。在这里,我们展示了在单细胞分辨率下使用空间转录组学分析完整的卡内基7期人类胚胎,以及在第二个胚胎中进行免疫荧光验证。利用82个连续冷冻切片和立体测序技术,我们重建了胚胎的三维模型。我们的研究结果揭示了不同的中胚层亚型的早期规范和前内脏内胚层的存在。值得注意的是,原始生殖细胞位于连接柄中,卵黄囊中观察到造血干细胞独立造血。这项研究促进了我们对人类原肠胚形成的理解,并为未来人类早期发育的研究提供了有价值的数据。
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来源期刊
Nature Cell Biology
Nature Cell Biology 生物-细胞生物学
CiteScore
28.40
自引率
0.90%
发文量
219
审稿时长
3 months
期刊介绍: Nature Cell Biology, a prestigious journal, upholds a commitment to publishing papers of the highest quality across all areas of cell biology, with a particular focus on elucidating mechanisms underlying fundamental cell biological processes. The journal's broad scope encompasses various areas of interest, including but not limited to: -Autophagy -Cancer biology -Cell adhesion and migration -Cell cycle and growth -Cell death -Chromatin and epigenetics -Cytoskeletal dynamics -Developmental biology -DNA replication and repair -Mechanisms of human disease -Mechanobiology -Membrane traffic and dynamics -Metabolism -Nuclear organization and dynamics -Organelle biology -Proteolysis and quality control -RNA biology -Signal transduction -Stem cell biology
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