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Bioengineered embryoids mimic post-implantation development in vitro.


ABSTRACT: The difficulty of studying post-implantation development in mammals has sparked a flurry of activity to develop in vitro models, termed embryoids, based on self-organizing pluripotent stem cells. Previous approaches to derive embryoids either lack the physiological morphology and signaling interactions, or are unconducive to model post-gastrulation development. Here, we report a bioengineering-inspired approach aimed at addressing this gap. We employ a high-throughput cell aggregation approach to simultaneously coax mouse embryonic stem cells into hundreds of uniform epiblast-like aggregates in a solid matrix-free manner. When co-cultured with mouse trophoblast stem cell aggregates, the resulting hybrid structures initiate gastrulation-like events and undergo axial morphogenesis to yield structures, termed EpiTS embryoids, with a pronounced anterior development, including brain-like regions. We identify the presence of an epithelium in EPI aggregates as the major determinant for the axial morphogenesis and anterior development seen in EpiTS embryoids. Our results demonstrate the potential of EpiTS embryoids to study peri-gastrulation development in vitro.

SUBMITTER: Girgin MU 

PROVIDER: S-EPMC8390504 | biostudies-literature | 2021 Aug

REPOSITORIES: biostudies-literature

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Bioengineered embryoids mimic post-implantation development in vitro.

Girgin Mehmet U MU   Broguiere Nicolas N   Hoehnel Sylke S   Brandenberg Nathalie N   Mercier Bastien B   Arias Alfonso Martinez AM   Lutolf Matthias P MP  

Nature communications 20210826 1


The difficulty of studying post-implantation development in mammals has sparked a flurry of activity to develop in vitro models, termed embryoids, based on self-organizing pluripotent stem cells. Previous approaches to derive embryoids either lack the physiological morphology and signaling interactions, or are unconducive to model post-gastrulation development. Here, we report a bioengineering-inspired approach aimed at addressing this gap. We employ a high-throughput cell aggregation approach t  ...[more]

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