Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Alhashem, Zain, Camargo-Sosa, Karen, Kelsh, Robert N., Linker, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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
_version_ 1784730977026703360
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
work_keys_str_mv AT alhashemzain trunkneuralcrestmigratorypositionandasymmetricdivisionpredictterminaldifferentiation
AT camargososakaren trunkneuralcrestmigratorypositionandasymmetricdivisionpredictterminaldifferentiation
AT kelshrobertn trunkneuralcrestmigratorypositionandasymmetricdivisionpredictterminaldifferentiation
AT linkerclaudia trunkneuralcrestmigratorypositionandasymmetricdivisionpredictterminaldifferentiation