A transgene-free, human peri-gastrulation embryo model with trilaminar embryonic disc-, amnion- and yolk sac-like structures

Shiyu Sun, Yi Zheng, Yung Su Kim, Zheng Zhong, Norio Kobayashi, Xufeng Xue, Yue Liu, Zhuowei Zhou, Yanhong Xu, Jinglei Zhai, Hongmei Wang, Jianping Fu
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Abstract

The ultimate outcome of the gastrulation in mammalian development is a recognizable trilaminar disc structure containing organized cell lineages with spatially defined identities in an emerging coordinate system1–4. Despite its importance in human development, gastrulation remains difficult to study. Stem cell-based embryo models, including those that recapitulate different aspects of pre- and peri-gastrulation human development5–15, are emerging as promising tools for studying human embryogenesis16–18. However, it remains unclear whether existing human embryo models are capable of modeling the development of the trilaminar embryonic disc structure, a hallmark of human gastrulation. Here we report a transgene-free human embryo model derived solely from primed human pluripotent stem cells (hPSCs), which recapitulates various aspects of peri-gastrulation human development, including formation of trilaminar embryonic layers situated between dorsal amnion and ventral definitive yolk sac and primary hematopoiesis. We term this model the peri-gastrulation trilaminar embryonic disc (PTED) embryoid. The development of PTED embryoid does not follow natural developmental sequences of cell lineage diversification or spatial organization. Instead, it exploits both extrinsic control of tissue boundaries and intrinsic self-organizing properties and embryonic plasticity of the diverse peri-gastrulation-stage cell lineages, leading to the emergence of in vivo-like tissue organization and function at a global scale. Our lineage tracing study reveals that in PTED embryoids, embryonic and extraembryonic mesoderm cells, as well as embryonic and extraembryonic endoderm cells, share common progenitors emerging during peri-gastrulation development. Active hematopoiesis and blood cell generation are evident in the yolk sac-like structure of PTED embryoids. Together, PTED embryoids provide a promising and ethically less challenging model for studying self-organizing properties of peri-gastrulation human development.
具有三层胚盘、羊膜和卵黄囊样结构的无转基因围胃期人类胚胎模型
在哺乳动物的发育过程中,胃形成的最终结果是一个可识别的三叶盘结构,其中包含有组织的细胞系,这些细胞系在新出现的坐标系统中具有空间上明确的特征1-4。尽管 gastrulation 在人类发育过程中非常重要,但它仍然难以研究。以干细胞为基础的胚胎模型,包括那些能再现人类胚胎发育前期和后期不同方面的胚胎模型5-15,正逐渐成为研究人类胚胎发生的有前途的工具16-18。然而,现有的人类胚胎模型是否能模拟三层胚盘结构的发育仍不清楚,而三层胚盘结构是人类胃发育的标志。在此,我们报告了一种完全由原始人类多能干细胞(hPSCs)衍生的无转基因人类胚胎模型,该模型再现了人类围胃发育的各个方面,包括位于背侧羊膜和腹侧最终卵黄囊之间的三层胚胎层的形成以及初级造血。我们将这一模型称为围胃三层胚盘(PTED)胚胎。PTED胚盘的发育并不遵循细胞系分化或空间组织的自然发育顺序。相反,它既利用了组织边界的外在控制,也利用了围胃期不同细胞系的内在自组织特性和胚胎可塑性,从而在全球范围内形成了类似活体组织的组织和功能。我们的细胞系追踪研究揭示,在 PTED 胚胎中,胚胎和胚外中胚层细胞以及胚胎和胚外内胚层细胞在围胃发育期有共同的祖细胞。在 PTED 胚胎的卵黄囊状结构中,造血和血细胞生成十分活跃。总之,PTED 胚胎为研究人类围孕期发育的自组织特性提供了一个前景广阔、伦理挑战较小的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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