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人类干细胞自我成形成植后谱系。

Self-patterning of human stem cells into post-implantation lineages.

机构信息

Department of Genetics, Yale School of Medicine, Yale University, New Haven, CT, USA.

Yale Stem Cell Center, Yale University, New Haven, CT, USA.

出版信息

Nature. 2023 Oct;622(7983):574-583. doi: 10.1038/s41586-023-06354-4. Epub 2023 Jun 27.

DOI:10.1038/s41586-023-06354-4
PMID:37369348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10584676/
Abstract

Investigating human development is a substantial scientific challenge due to the technical and ethical limitations of working with embryonic samples. In the face of these difficulties, stem cells have provided an alternative to experimentally model inaccessible stages of human development in vitro. Here we show that human pluripotent stem cells can be triggered to self-organize into three-dimensional structures that recapitulate some key spatiotemporal events of early human post-implantation embryonic development. Our system reproducibly captures spontaneous differentiation and co-development of embryonic epiblast-like and extra-embryonic hypoblast-like lineages, establishes key signalling hubs with secreted modulators and undergoes symmetry breaking-like events. Single-cell transcriptomics confirms differentiation into diverse cell states of the perigastrulating human embryo without establishing placental cell types, including signatures of post-implantation epiblast, amniotic ectoderm, primitive streak, mesoderm, early extra-embryonic endoderm, as well as initial yolk sac induction. Collectively, our system captures key features of human embryonic development spanning from Carnegie stage 4-7, offering a reproducible, tractable and scalable experimental platform to understand the basic cellular and molecular mechanisms that underlie human development, including new opportunities to dissect congenital pathologies with high throughput.

摘要

研究人类发育是一项重大的科学挑战,因为在胚胎样本上进行实验存在技术和伦理限制。面对这些困难,干细胞为在体外模拟人类发育的不可接近阶段提供了一种替代方法。在这里,我们展示了人类多能干细胞可以被触发自组织成三维结构,这些结构再现了早期人类植入后胚胎发育的一些关键时空事件。我们的系统可重现自发分化和胚胎外胚层样和胚胎外胚层样谱系的共同发育,建立具有分泌调节剂的关键信号枢纽,并经历类似对称性破缺的事件。单细胞转录组学证实,该系统可以分化为具有不同细胞状态的围胚层人类胚胎,而无需建立胎盘细胞类型,包括植入后外胚层、羊膜外胚层、原始条纹、中胚层、早期胚胎外内胚层以及最初的卵黄囊诱导的特征。总的来说,我们的系统捕获了跨越卡内基阶段 4-7 的人类胚胎发育的关键特征,提供了一个可重现、易于处理和可扩展的实验平台,以了解人类发育的基本细胞和分子机制,包括利用高通量技术解析先天性病理的新机会。

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