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Trunk Neural Crest Migratory Position and Asymmetric Division Predict Terminal Differentiation
The generation of complex structures during embryogenesis requires the controlled migration and differentiation of cells from distant origins. How these processes are coordinated and impact each other to form functional structures is not fully understood. Neural crest cells migrate extensively givin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214262/ https://www.ncbi.nlm.nih.gov/pubmed/35756992 http://dx.doi.org/10.3389/fcell.2022.887393 |
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author | Alhashem, Zain Camargo-Sosa, Karen Kelsh, Robert N. Linker, Claudia |
author_facet | Alhashem, Zain Camargo-Sosa, Karen Kelsh, Robert N. Linker, Claudia |
author_sort | Alhashem, Zain |
collection | PubMed |
description | The generation of complex structures during embryogenesis requires the controlled migration and differentiation of cells from distant origins. How these processes are coordinated and impact each other to form functional structures is not fully understood. Neural crest cells migrate extensively giving rise to many cell types. In the trunk, neural crest cells migrate collectively forming chains comprised of cells with distinct migratory identities: one leader cell at the front of the group directs migration, while followers track the leader forming the body of the chain. Herein we analysed the relationship between trunk neural crest migratory identity and terminal differentiation. We found that trunk neural crest migration and fate allocation is coherent. Leader cells that initiate movement give rise to the most distal derivativities. Interestingly, the asymmetric division of leaders separates migratory identity and fate. The distal daughter cell retains the leader identity and clonally forms the Sympathetic Ganglia. The proximal sibling migrates as a follower and gives rise to Schwann cells. The sympathetic neuron transcription factor phox2bb is strongly expressed by leaders from early stages of migration, suggesting that specification and migration occur concomitantly and in coordination. Followers divide symmetrically and their fate correlates with their position in the chain. |
format | Online Article Text |
id | pubmed-9214262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92142622022-06-23 Trunk Neural Crest Migratory Position and Asymmetric Division Predict Terminal Differentiation Alhashem, Zain Camargo-Sosa, Karen Kelsh, Robert N. Linker, Claudia Front Cell Dev Biol Cell and Developmental Biology The generation of complex structures during embryogenesis requires the controlled migration and differentiation of cells from distant origins. How these processes are coordinated and impact each other to form functional structures is not fully understood. Neural crest cells migrate extensively giving rise to many cell types. In the trunk, neural crest cells migrate collectively forming chains comprised of cells with distinct migratory identities: one leader cell at the front of the group directs migration, while followers track the leader forming the body of the chain. Herein we analysed the relationship between trunk neural crest migratory identity and terminal differentiation. We found that trunk neural crest migration and fate allocation is coherent. Leader cells that initiate movement give rise to the most distal derivativities. Interestingly, the asymmetric division of leaders separates migratory identity and fate. The distal daughter cell retains the leader identity and clonally forms the Sympathetic Ganglia. The proximal sibling migrates as a follower and gives rise to Schwann cells. The sympathetic neuron transcription factor phox2bb is strongly expressed by leaders from early stages of migration, suggesting that specification and migration occur concomitantly and in coordination. Followers divide symmetrically and their fate correlates with their position in the chain. Frontiers Media S.A. 2022-06-08 /pmc/articles/PMC9214262/ /pubmed/35756992 http://dx.doi.org/10.3389/fcell.2022.887393 Text en Copyright © 2022 Alhashem, Camargo-Sosa, Kelsh and Linker. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Alhashem, Zain Camargo-Sosa, Karen Kelsh, Robert N. Linker, Claudia Trunk Neural Crest Migratory Position and Asymmetric Division Predict Terminal Differentiation |
title | Trunk Neural Crest Migratory Position and Asymmetric Division Predict Terminal Differentiation |
title_full | Trunk Neural Crest Migratory Position and Asymmetric Division Predict Terminal Differentiation |
title_fullStr | Trunk Neural Crest Migratory Position and Asymmetric Division Predict Terminal Differentiation |
title_full_unstemmed | Trunk Neural Crest Migratory Position and Asymmetric Division Predict Terminal Differentiation |
title_short | Trunk Neural Crest Migratory Position and Asymmetric Division Predict Terminal Differentiation |
title_sort | trunk neural crest migratory position and asymmetric division predict terminal differentiation |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214262/ https://www.ncbi.nlm.nih.gov/pubmed/35756992 http://dx.doi.org/10.3389/fcell.2022.887393 |
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