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Pluripotent stem cell-derived model of the post-implantation human embryo.
Weatherbee, Bailey A T; Gantner, Carlos W; Iwamoto-Stohl, Lisa K; Daza, Riza M; Hamazaki, Nobuhiko; Shendure, Jay; Zernicka-Goetz, Magdalena.
  • Weatherbee BAT; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
  • Gantner CW; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
  • Iwamoto-Stohl LK; Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
  • Daza RM; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
  • Hamazaki N; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
  • Shendure J; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
  • Zernicka-Goetz M; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA.
Nature ; 622(7983): 584-593, 2023 Oct.
Article en En | MEDLINE | ID: mdl-37369347
ABSTRACT
The human embryo undergoes morphogenetic transformations following implantation into the uterus, but our knowledge of this crucial stage is limited by the inability to observe the embryo in vivo. Models of the embryo derived from stem cells are important tools for interrogating developmental events and tissue-tissue crosstalk during these stages1. Here we establish a model of the human post-implantation embryo, a human embryoid, comprising embryonic and extraembryonic tissues. We combine two types of extraembryonic-like cell generated by overexpression of transcription factors with wild-type embryonic stem cells and promote their self-organization into structures that mimic several aspects of the post-implantation human embryo. These self-organized aggregates contain a pluripotent epiblast-like domain surrounded by extraembryonic-like tissues. Our functional studies demonstrate that the epiblast-like domain robustly differentiates into amnion, extraembryonic mesenchyme and primordial germ cell-like cells in response to bone morphogenetic protein cues. In addition, we identify an inhibitory role for SOX17 in the specification of anterior hypoblast-like cells2. Modulation of the subpopulations in the hypoblast-like compartment demonstrates that extraembryonic-like cells influence epiblast-like domain differentiation, highlighting functional tissue-tissue crosstalk. In conclusion, we present a modular, tractable, integrated3 model of the human embryo that will enable us to probe key questions of human post-implantation development, a critical window during which substantial numbers of pregnancies fail.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Implantación del Embrión / Células Madre Pluripotentes / Desarrollo Embrionario / Embrión de Mamíferos / Modelos Biológicos Tipo de estudio: Prognostic_studies Límite: Female / Humans / Pregnancy Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Implantación del Embrión / Células Madre Pluripotentes / Desarrollo Embrionario / Embrión de Mamíferos / Modelos Biológicos Tipo de estudio: Prognostic_studies Límite: Female / Humans / Pregnancy Idioma: En Año: 2023 Tipo del documento: Article