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Embyoid organizer

GSE244033 Mus musculus Expression profiling by high throughput sequencing 8 samples Submitted 2024/12/09 Platform GPL24247
Summary
Recapitulation of development in vitro relies primarily on treatment of progenitor cells with media-borne morphogens, without the complex spatial instructions normally presented by native developmental niches. Here we build simple spatially asymmetric developmental niches by engineering synthetic organizer cells that self-assemble around stem cells and provide spatially-defined morphogenic instructions. Using a toolkit of natural and engineered adhesion molecules we harness differential adhesion to program the formation of specific organizer cell geometries around the stem cells, allowing the generation of morphogen gradients with tunable position, amplitude, and signal types. Synthetic niches presenting the antagonistic morphogens WNT3A and DKK1 were used to guide development of pluripotent stem cells. These synthetic organizers generated distinct morphological outcomes, including formation of a beating heart-like chamber and embryoids containing a complement of diverse cell lineages derived from mesoderm, endoderm and ectoderm. The resulting morphologies were reproducible in high-throughput format. Spatially programmable synthetic organizer cells, which integrate the principles of differential adhesion and positional information, thus provide a systematic approach to guide, recapitulate, and modify development in a controlled fashion.
Published in
Synthetic organizer cells guide development via spatial and biochemical instructions
Yamada T, Trentesaux C, Brunger JM et al. · Cell 2025 · PMID 39706189 · doi:10.1016/j.cell.2024.11.017
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Also filed as BioProject PRJNA1021143 and SRA study SRP463292. Searching any of these in the dataset finder brings you back here.

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