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A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle

In most vertebrates, the upper digestive tract is composed of muscularized jaws linked to the esophagus that permits food ingestion and swallowing. Masticatory and esophagus striated muscles (ESM) share a common cardiopharyngeal mesoderm (CPM) origin, however ESM are unusual among striated muscles a...

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Autores principales: Comai, Glenda, Heude, Eglantine, Mella, Sebastian, Paisant, Sylvain, Pala, Francesca, Gallardo, Mirialys, Langa, Francina, Kardon, Gabrielle, Gopalakrishnan, Swetha, Tajbakhsh, Shahragim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752947/
https://www.ncbi.nlm.nih.gov/pubmed/31535973
http://dx.doi.org/10.7554/eLife.47460
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author Comai, Glenda
Heude, Eglantine
Mella, Sebastian
Paisant, Sylvain
Pala, Francesca
Gallardo, Mirialys
Langa, Francina
Kardon, Gabrielle
Gopalakrishnan, Swetha
Tajbakhsh, Shahragim
author_facet Comai, Glenda
Heude, Eglantine
Mella, Sebastian
Paisant, Sylvain
Pala, Francesca
Gallardo, Mirialys
Langa, Francina
Kardon, Gabrielle
Gopalakrishnan, Swetha
Tajbakhsh, Shahragim
author_sort Comai, Glenda
collection PubMed
description In most vertebrates, the upper digestive tract is composed of muscularized jaws linked to the esophagus that permits food ingestion and swallowing. Masticatory and esophagus striated muscles (ESM) share a common cardiopharyngeal mesoderm (CPM) origin, however ESM are unusual among striated muscles as they are established in the absence of a primary skeletal muscle scaffold. Using mouse chimeras, we show that the transcription factors Tbx1 and Isl1 are required cell-autonomously for myogenic specification of ESM progenitors. Further, genetic loss-of-function and pharmacological studies point to MET/HGF signaling for antero-posterior migration of esophagus muscle progenitors, where Hgf ligand is expressed in adjacent smooth muscle cells. These observations highlight the functional relevance of a smooth and striated muscle progenitor dialogue for ESM patterning. Our findings establish a Tbx1-Isl1-Met genetic hierarchy that uniquely regulates esophagus myogenesis and identify distinct genetic signatures that can be used as framework to interpret pathologies arising within CPM derivatives.
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spelling pubmed-67529472019-09-20 A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle Comai, Glenda Heude, Eglantine Mella, Sebastian Paisant, Sylvain Pala, Francesca Gallardo, Mirialys Langa, Francina Kardon, Gabrielle Gopalakrishnan, Swetha Tajbakhsh, Shahragim eLife Developmental Biology In most vertebrates, the upper digestive tract is composed of muscularized jaws linked to the esophagus that permits food ingestion and swallowing. Masticatory and esophagus striated muscles (ESM) share a common cardiopharyngeal mesoderm (CPM) origin, however ESM are unusual among striated muscles as they are established in the absence of a primary skeletal muscle scaffold. Using mouse chimeras, we show that the transcription factors Tbx1 and Isl1 are required cell-autonomously for myogenic specification of ESM progenitors. Further, genetic loss-of-function and pharmacological studies point to MET/HGF signaling for antero-posterior migration of esophagus muscle progenitors, where Hgf ligand is expressed in adjacent smooth muscle cells. These observations highlight the functional relevance of a smooth and striated muscle progenitor dialogue for ESM patterning. Our findings establish a Tbx1-Isl1-Met genetic hierarchy that uniquely regulates esophagus myogenesis and identify distinct genetic signatures that can be used as framework to interpret pathologies arising within CPM derivatives. eLife Sciences Publications, Ltd 2019-09-19 /pmc/articles/PMC6752947/ /pubmed/31535973 http://dx.doi.org/10.7554/eLife.47460 Text en © 2019, Comai et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Comai, Glenda
Heude, Eglantine
Mella, Sebastian
Paisant, Sylvain
Pala, Francesca
Gallardo, Mirialys
Langa, Francina
Kardon, Gabrielle
Gopalakrishnan, Swetha
Tajbakhsh, Shahragim
A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle
title A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle
title_full A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle
title_fullStr A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle
title_full_unstemmed A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle
title_short A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle
title_sort distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752947/
https://www.ncbi.nlm.nih.gov/pubmed/31535973
http://dx.doi.org/10.7554/eLife.47460
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