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Spatiotemporal cellular movement and fate decisions during first pharyngeal arch morphogenesis
Cranial neural crest (CNC) cells contribute to different cell types during embryonic development. It is unknown whether postmigratory CNC cells undergo dynamic cellular movement and how the process of cell fate decision occurs within the first pharyngeal arch (FPA). Our investigations demonstrate no...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744069/ https://www.ncbi.nlm.nih.gov/pubmed/33328221 http://dx.doi.org/10.1126/sciadv.abb0119 |
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author | Yuan, Yuan Loh, Yong-hwee Eddie Han, Xia Feng, Jifan Ho, Thach-Vu He, Jinzhi Jing, Junjun Groff, Kimberly Wu, Alan Chai, Yang |
author_facet | Yuan, Yuan Loh, Yong-hwee Eddie Han, Xia Feng, Jifan Ho, Thach-Vu He, Jinzhi Jing, Junjun Groff, Kimberly Wu, Alan Chai, Yang |
author_sort | Yuan, Yuan |
collection | PubMed |
description | Cranial neural crest (CNC) cells contribute to different cell types during embryonic development. It is unknown whether postmigratory CNC cells undergo dynamic cellular movement and how the process of cell fate decision occurs within the first pharyngeal arch (FPA). Our investigations demonstrate notable heterogeneity within the CNC cells, refine the patterning domains, and identify progenitor cells within the FPA. These progenitor cells undergo fate bifurcation that separates them into common progenitors and mesenchymal cells, which are characterized by Cdk1 and Spry2/Notch2 expression, respectively. The common progenitors undergo further bifurcations to restrict them into osteogenic/odontogenic and chondrogenic/fibroblast lineages. Disruption of a patterning domain leads to specific mandible and tooth defects, validating the binary cell fate restriction process. Different from the compartment model of mandibular morphogenesis, our data redefine heterogeneous cellular domains within the FPA, reveal dynamic cellular movement in time, and describe a sequential series of binary cell fate decision-making process. |
format | Online Article Text |
id | pubmed-7744069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-77440692021-01-04 Spatiotemporal cellular movement and fate decisions during first pharyngeal arch morphogenesis Yuan, Yuan Loh, Yong-hwee Eddie Han, Xia Feng, Jifan Ho, Thach-Vu He, Jinzhi Jing, Junjun Groff, Kimberly Wu, Alan Chai, Yang Sci Adv Research Articles Cranial neural crest (CNC) cells contribute to different cell types during embryonic development. It is unknown whether postmigratory CNC cells undergo dynamic cellular movement and how the process of cell fate decision occurs within the first pharyngeal arch (FPA). Our investigations demonstrate notable heterogeneity within the CNC cells, refine the patterning domains, and identify progenitor cells within the FPA. These progenitor cells undergo fate bifurcation that separates them into common progenitors and mesenchymal cells, which are characterized by Cdk1 and Spry2/Notch2 expression, respectively. The common progenitors undergo further bifurcations to restrict them into osteogenic/odontogenic and chondrogenic/fibroblast lineages. Disruption of a patterning domain leads to specific mandible and tooth defects, validating the binary cell fate restriction process. Different from the compartment model of mandibular morphogenesis, our data redefine heterogeneous cellular domains within the FPA, reveal dynamic cellular movement in time, and describe a sequential series of binary cell fate decision-making process. American Association for the Advancement of Science 2020-12-16 /pmc/articles/PMC7744069/ /pubmed/33328221 http://dx.doi.org/10.1126/sciadv.abb0119 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Yuan, Yuan Loh, Yong-hwee Eddie Han, Xia Feng, Jifan Ho, Thach-Vu He, Jinzhi Jing, Junjun Groff, Kimberly Wu, Alan Chai, Yang Spatiotemporal cellular movement and fate decisions during first pharyngeal arch morphogenesis |
title | Spatiotemporal cellular movement and fate decisions during first pharyngeal arch morphogenesis |
title_full | Spatiotemporal cellular movement and fate decisions during first pharyngeal arch morphogenesis |
title_fullStr | Spatiotemporal cellular movement and fate decisions during first pharyngeal arch morphogenesis |
title_full_unstemmed | Spatiotemporal cellular movement and fate decisions during first pharyngeal arch morphogenesis |
title_short | Spatiotemporal cellular movement and fate decisions during first pharyngeal arch morphogenesis |
title_sort | spatiotemporal cellular movement and fate decisions during first pharyngeal arch morphogenesis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744069/ https://www.ncbi.nlm.nih.gov/pubmed/33328221 http://dx.doi.org/10.1126/sciadv.abb0119 |
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