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Charting human development using a multi-endodermal organ atlas and organoid models
Organs are composed of diverse cell types that traverse transient states during organogenesis. To interrogate this diversity during human development, we generate a single-cell transcriptome atlas from multiple developing endodermal organs of the respiratory and gastrointestinal tract. We illuminate...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208823/ https://www.ncbi.nlm.nih.gov/pubmed/34019796 http://dx.doi.org/10.1016/j.cell.2021.04.028 |
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author | Yu, Qianhui Kilik, Umut Holloway, Emily M. Tsai, Yu-Hwai Harmel, Christoph Wu, Angeline Wu, Joshua H. Czerwinski, Michael Childs, Charlie J. He, Zhisong Capeling, Meghan M. Huang, Sha Glass, Ian A. Higgins, Peter D.R. Treutlein, Barbara Spence, Jason R. Camp, J. Gray |
author_facet | Yu, Qianhui Kilik, Umut Holloway, Emily M. Tsai, Yu-Hwai Harmel, Christoph Wu, Angeline Wu, Joshua H. Czerwinski, Michael Childs, Charlie J. He, Zhisong Capeling, Meghan M. Huang, Sha Glass, Ian A. Higgins, Peter D.R. Treutlein, Barbara Spence, Jason R. Camp, J. Gray |
author_sort | Yu, Qianhui |
collection | PubMed |
description | Organs are composed of diverse cell types that traverse transient states during organogenesis. To interrogate this diversity during human development, we generate a single-cell transcriptome atlas from multiple developing endodermal organs of the respiratory and gastrointestinal tract. We illuminate cell states, transcription factors, and organ-specific epithelial stem cell and mesenchyme interactions across lineages. We implement the atlas as a high-dimensional search space to benchmark human pluripotent stem cell (hPSC)-derived intestinal organoids (HIOs) under multiple culture conditions. We show that HIOs recapitulate reference cell states and use HIOs to reconstruct the molecular dynamics of intestinal epithelium and mesenchyme emergence. We show that the mesenchyme-derived niche cue NRG1 enhances intestinal stem cell maturation in vitro and that the homeobox transcription factor CDX2 is required for regionalization of intestinal epithelium and mesenchyme in humans. This work combines cell atlases and organoid technologies to understand how human organ development is orchestrated. |
format | Online Article Text |
id | pubmed-8208823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82088232021-06-25 Charting human development using a multi-endodermal organ atlas and organoid models Yu, Qianhui Kilik, Umut Holloway, Emily M. Tsai, Yu-Hwai Harmel, Christoph Wu, Angeline Wu, Joshua H. Czerwinski, Michael Childs, Charlie J. He, Zhisong Capeling, Meghan M. Huang, Sha Glass, Ian A. Higgins, Peter D.R. Treutlein, Barbara Spence, Jason R. Camp, J. Gray Cell Resource Organs are composed of diverse cell types that traverse transient states during organogenesis. To interrogate this diversity during human development, we generate a single-cell transcriptome atlas from multiple developing endodermal organs of the respiratory and gastrointestinal tract. We illuminate cell states, transcription factors, and organ-specific epithelial stem cell and mesenchyme interactions across lineages. We implement the atlas as a high-dimensional search space to benchmark human pluripotent stem cell (hPSC)-derived intestinal organoids (HIOs) under multiple culture conditions. We show that HIOs recapitulate reference cell states and use HIOs to reconstruct the molecular dynamics of intestinal epithelium and mesenchyme emergence. We show that the mesenchyme-derived niche cue NRG1 enhances intestinal stem cell maturation in vitro and that the homeobox transcription factor CDX2 is required for regionalization of intestinal epithelium and mesenchyme in humans. This work combines cell atlases and organoid technologies to understand how human organ development is orchestrated. Cell Press 2021-06-10 /pmc/articles/PMC8208823/ /pubmed/34019796 http://dx.doi.org/10.1016/j.cell.2021.04.028 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Resource Yu, Qianhui Kilik, Umut Holloway, Emily M. Tsai, Yu-Hwai Harmel, Christoph Wu, Angeline Wu, Joshua H. Czerwinski, Michael Childs, Charlie J. He, Zhisong Capeling, Meghan M. Huang, Sha Glass, Ian A. Higgins, Peter D.R. Treutlein, Barbara Spence, Jason R. Camp, J. Gray Charting human development using a multi-endodermal organ atlas and organoid models |
title | Charting human development using a multi-endodermal organ atlas and organoid models |
title_full | Charting human development using a multi-endodermal organ atlas and organoid models |
title_fullStr | Charting human development using a multi-endodermal organ atlas and organoid models |
title_full_unstemmed | Charting human development using a multi-endodermal organ atlas and organoid models |
title_short | Charting human development using a multi-endodermal organ atlas and organoid models |
title_sort | charting human development using a multi-endodermal organ atlas and organoid models |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208823/ https://www.ncbi.nlm.nih.gov/pubmed/34019796 http://dx.doi.org/10.1016/j.cell.2021.04.028 |
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