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The single-cell and spatial transcriptional landscape of human gastrulation and early brain development
The emergence of the three germ layers and the lineage-specific precursor cells orchestrating organogenesis represent fundamental milestones during early embryonic development. We analyzed the transcriptional profiles of over 400,000 cells from 14 human samples collected from post-conceptional weeks...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241223/ https://www.ncbi.nlm.nih.gov/pubmed/37192616 http://dx.doi.org/10.1016/j.stem.2023.04.016 |
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author | Zeng, Bo Liu, Zeyuan Lu, Yufeng Zhong, Suijuan Qin, Shenyue Huang, Luwei Zeng, Yang Li, Zixiao Dong, Hao Shi, Yingchao Yang, Jialei Dai, Yalun Ma, Qiang Sun, Le Bian, Lihong Han, Dan Chen, Youqiao Qiu, Xin Wang, Wei Marín, Oscar Wu, Qian Wang, Yongjun Wang, Xiaoqun |
author_facet | Zeng, Bo Liu, Zeyuan Lu, Yufeng Zhong, Suijuan Qin, Shenyue Huang, Luwei Zeng, Yang Li, Zixiao Dong, Hao Shi, Yingchao Yang, Jialei Dai, Yalun Ma, Qiang Sun, Le Bian, Lihong Han, Dan Chen, Youqiao Qiu, Xin Wang, Wei Marín, Oscar Wu, Qian Wang, Yongjun Wang, Xiaoqun |
author_sort | Zeng, Bo |
collection | PubMed |
description | The emergence of the three germ layers and the lineage-specific precursor cells orchestrating organogenesis represent fundamental milestones during early embryonic development. We analyzed the transcriptional profiles of over 400,000 cells from 14 human samples collected from post-conceptional weeks (PCW) 3 to 12 to delineate the dynamic molecular and cellular landscape of early gastrulation and nervous system development. We described the diversification of cell types, the spatial patterning of neural tube cells, and the signaling pathways likely involved in transforming epiblast cells into neuroepithelial cells and then into radial glia. We resolved 24 clusters of radial glial cells along the neural tube and outlined differentiation trajectories for the main classes of neurons. Lastly, we identified conserved and distinctive features across species by comparing early embryonic single-cell transcriptomic profiles between humans and mice. This comprehensive atlas sheds light on the molecular mechanisms underlying gastrulation and early human brain development. |
format | Online Article Text |
id | pubmed-10241223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102412232023-06-06 The single-cell and spatial transcriptional landscape of human gastrulation and early brain development Zeng, Bo Liu, Zeyuan Lu, Yufeng Zhong, Suijuan Qin, Shenyue Huang, Luwei Zeng, Yang Li, Zixiao Dong, Hao Shi, Yingchao Yang, Jialei Dai, Yalun Ma, Qiang Sun, Le Bian, Lihong Han, Dan Chen, Youqiao Qiu, Xin Wang, Wei Marín, Oscar Wu, Qian Wang, Yongjun Wang, Xiaoqun Cell Stem Cell Resource The emergence of the three germ layers and the lineage-specific precursor cells orchestrating organogenesis represent fundamental milestones during early embryonic development. We analyzed the transcriptional profiles of over 400,000 cells from 14 human samples collected from post-conceptional weeks (PCW) 3 to 12 to delineate the dynamic molecular and cellular landscape of early gastrulation and nervous system development. We described the diversification of cell types, the spatial patterning of neural tube cells, and the signaling pathways likely involved in transforming epiblast cells into neuroepithelial cells and then into radial glia. We resolved 24 clusters of radial glial cells along the neural tube and outlined differentiation trajectories for the main classes of neurons. Lastly, we identified conserved and distinctive features across species by comparing early embryonic single-cell transcriptomic profiles between humans and mice. This comprehensive atlas sheds light on the molecular mechanisms underlying gastrulation and early human brain development. Cell Press 2023-06-01 /pmc/articles/PMC10241223/ /pubmed/37192616 http://dx.doi.org/10.1016/j.stem.2023.04.016 Text en © 2023 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 Zeng, Bo Liu, Zeyuan Lu, Yufeng Zhong, Suijuan Qin, Shenyue Huang, Luwei Zeng, Yang Li, Zixiao Dong, Hao Shi, Yingchao Yang, Jialei Dai, Yalun Ma, Qiang Sun, Le Bian, Lihong Han, Dan Chen, Youqiao Qiu, Xin Wang, Wei Marín, Oscar Wu, Qian Wang, Yongjun Wang, Xiaoqun The single-cell and spatial transcriptional landscape of human gastrulation and early brain development |
title | The single-cell and spatial transcriptional landscape of human gastrulation and early brain development |
title_full | The single-cell and spatial transcriptional landscape of human gastrulation and early brain development |
title_fullStr | The single-cell and spatial transcriptional landscape of human gastrulation and early brain development |
title_full_unstemmed | The single-cell and spatial transcriptional landscape of human gastrulation and early brain development |
title_short | The single-cell and spatial transcriptional landscape of human gastrulation and early brain development |
title_sort | single-cell and spatial transcriptional landscape of human gastrulation and early brain development |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241223/ https://www.ncbi.nlm.nih.gov/pubmed/37192616 http://dx.doi.org/10.1016/j.stem.2023.04.016 |
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