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Notch signalling regulates epibranchial placode patterning and segregation

Epibranchial placodes are the geniculate, petrosal and nodose placodes that generate parts of cranial nerves VII, IX and X, respectively. How the three spatially separated placodes are derived from the common posterior placodal area is poorly understood. Here, we reveal that the broad posterior plac...

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Autores principales: Wang, Li, Xie, Junjie, Zhang, Haoran, Tsang, Long Hin, Tsang, Sze Lan, Braune, Eike-Benjamin, Lendahl, Urban, Sham, Mai Har
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044445/
https://www.ncbi.nlm.nih.gov/pubmed/31988190
http://dx.doi.org/10.1242/dev.183665
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author Wang, Li
Xie, Junjie
Zhang, Haoran
Tsang, Long Hin
Tsang, Sze Lan
Braune, Eike-Benjamin
Lendahl, Urban
Sham, Mai Har
author_facet Wang, Li
Xie, Junjie
Zhang, Haoran
Tsang, Long Hin
Tsang, Sze Lan
Braune, Eike-Benjamin
Lendahl, Urban
Sham, Mai Har
author_sort Wang, Li
collection PubMed
description Epibranchial placodes are the geniculate, petrosal and nodose placodes that generate parts of cranial nerves VII, IX and X, respectively. How the three spatially separated placodes are derived from the common posterior placodal area is poorly understood. Here, we reveal that the broad posterior placode area is first patterned into a Vgll2(+)/Irx5(+) rostral domain and a Sox2(+)/Fgf3(+)/Etv5(+) caudal domain relative to the first pharyngeal cleft. This initial rostral and caudal patterning is then sequentially repeated along each pharyngeal cleft for each epibranchial placode. The caudal domains give rise to the neuronal and non-neuronal cells in the placode, whereas the rostral domains are previously unrecognized structures, serving as spacers between the final placodes. Notch signalling regulates the balance between the rostral and caudal domains: high levels of Notch signalling expand the caudal domain at the expense of the rostral domain, whereas loss of Notch signalling produces the converse phenotype. Collectively, these data unravel a new patterning principle for the early phases of epibranchial placode development and a role for Notch signalling in orchestrating epibranchial placode segregation and differentiation.
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spelling pubmed-70444452020-03-12 Notch signalling regulates epibranchial placode patterning and segregation Wang, Li Xie, Junjie Zhang, Haoran Tsang, Long Hin Tsang, Sze Lan Braune, Eike-Benjamin Lendahl, Urban Sham, Mai Har Development Research Article Epibranchial placodes are the geniculate, petrosal and nodose placodes that generate parts of cranial nerves VII, IX and X, respectively. How the three spatially separated placodes are derived from the common posterior placodal area is poorly understood. Here, we reveal that the broad posterior placode area is first patterned into a Vgll2(+)/Irx5(+) rostral domain and a Sox2(+)/Fgf3(+)/Etv5(+) caudal domain relative to the first pharyngeal cleft. This initial rostral and caudal patterning is then sequentially repeated along each pharyngeal cleft for each epibranchial placode. The caudal domains give rise to the neuronal and non-neuronal cells in the placode, whereas the rostral domains are previously unrecognized structures, serving as spacers between the final placodes. Notch signalling regulates the balance between the rostral and caudal domains: high levels of Notch signalling expand the caudal domain at the expense of the rostral domain, whereas loss of Notch signalling produces the converse phenotype. Collectively, these data unravel a new patterning principle for the early phases of epibranchial placode development and a role for Notch signalling in orchestrating epibranchial placode segregation and differentiation. The Company of Biologists Ltd 2020-02-17 /pmc/articles/PMC7044445/ /pubmed/31988190 http://dx.doi.org/10.1242/dev.183665 Text en © 2020. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Wang, Li
Xie, Junjie
Zhang, Haoran
Tsang, Long Hin
Tsang, Sze Lan
Braune, Eike-Benjamin
Lendahl, Urban
Sham, Mai Har
Notch signalling regulates epibranchial placode patterning and segregation
title Notch signalling regulates epibranchial placode patterning and segregation
title_full Notch signalling regulates epibranchial placode patterning and segregation
title_fullStr Notch signalling regulates epibranchial placode patterning and segregation
title_full_unstemmed Notch signalling regulates epibranchial placode patterning and segregation
title_short Notch signalling regulates epibranchial placode patterning and segregation
title_sort notch signalling regulates epibranchial placode patterning and segregation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044445/
https://www.ncbi.nlm.nih.gov/pubmed/31988190
http://dx.doi.org/10.1242/dev.183665
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