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A neural crest cell isotropic-to-nematic phase transition in the developing mammalian gut
While the colonization of the embryonic gut by neural crest cells has been the subject of intense scrutiny over the past decades, we are only starting to grasp the morphogenetic transformations of the enteric nervous system happening in the fetal stage. Here, we show that enteric neural crest cell t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222382/ https://www.ncbi.nlm.nih.gov/pubmed/34162999 http://dx.doi.org/10.1038/s42003-021-02333-5 |
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author | Chevalier, Nicolas R. Ammouche, Yanis Gomis, Anthony Langlois, Lucas Guilbert, Thomas Bourdoncle, Pierre Dufour, Sylvie |
author_facet | Chevalier, Nicolas R. Ammouche, Yanis Gomis, Anthony Langlois, Lucas Guilbert, Thomas Bourdoncle, Pierre Dufour, Sylvie |
author_sort | Chevalier, Nicolas R. |
collection | PubMed |
description | While the colonization of the embryonic gut by neural crest cells has been the subject of intense scrutiny over the past decades, we are only starting to grasp the morphogenetic transformations of the enteric nervous system happening in the fetal stage. Here, we show that enteric neural crest cell transit during fetal development from an isotropic cell network to a square grid comprised of circumferentially-oriented cell bodies and longitudinally-extending interganglionic fibers. We present ex-vivo dynamic time-lapse imaging of this isotropic-to-nematic phase transition and show that it occurs concomitantly with circular smooth muscle differentiation in all regions of the gastrointestinal tract. Using conditional mutant embryos with enteric neural crest cells depleted of β1-integrins, we show that cell-extracellular matrix anchorage is necessary for ganglia to properly reorient. We demonstrate by whole mount second harmonic generation imaging that fibrous, circularly-spun collagen I fibers are in direct contact with neural crest cells during the orientation transition, providing an ideal orientation template. We conclude that smooth-muscle associated extracellular matrix drives a critical reorientation transition of the enteric nervous system in the mammalian fetus. |
format | Online Article Text |
id | pubmed-8222382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82223822021-07-09 A neural crest cell isotropic-to-nematic phase transition in the developing mammalian gut Chevalier, Nicolas R. Ammouche, Yanis Gomis, Anthony Langlois, Lucas Guilbert, Thomas Bourdoncle, Pierre Dufour, Sylvie Commun Biol Article While the colonization of the embryonic gut by neural crest cells has been the subject of intense scrutiny over the past decades, we are only starting to grasp the morphogenetic transformations of the enteric nervous system happening in the fetal stage. Here, we show that enteric neural crest cell transit during fetal development from an isotropic cell network to a square grid comprised of circumferentially-oriented cell bodies and longitudinally-extending interganglionic fibers. We present ex-vivo dynamic time-lapse imaging of this isotropic-to-nematic phase transition and show that it occurs concomitantly with circular smooth muscle differentiation in all regions of the gastrointestinal tract. Using conditional mutant embryos with enteric neural crest cells depleted of β1-integrins, we show that cell-extracellular matrix anchorage is necessary for ganglia to properly reorient. We demonstrate by whole mount second harmonic generation imaging that fibrous, circularly-spun collagen I fibers are in direct contact with neural crest cells during the orientation transition, providing an ideal orientation template. We conclude that smooth-muscle associated extracellular matrix drives a critical reorientation transition of the enteric nervous system in the mammalian fetus. Nature Publishing Group UK 2021-06-23 /pmc/articles/PMC8222382/ /pubmed/34162999 http://dx.doi.org/10.1038/s42003-021-02333-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Chevalier, Nicolas R. Ammouche, Yanis Gomis, Anthony Langlois, Lucas Guilbert, Thomas Bourdoncle, Pierre Dufour, Sylvie A neural crest cell isotropic-to-nematic phase transition in the developing mammalian gut |
title | A neural crest cell isotropic-to-nematic phase transition in the developing mammalian gut |
title_full | A neural crest cell isotropic-to-nematic phase transition in the developing mammalian gut |
title_fullStr | A neural crest cell isotropic-to-nematic phase transition in the developing mammalian gut |
title_full_unstemmed | A neural crest cell isotropic-to-nematic phase transition in the developing mammalian gut |
title_short | A neural crest cell isotropic-to-nematic phase transition in the developing mammalian gut |
title_sort | neural crest cell isotropic-to-nematic phase transition in the developing mammalian gut |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222382/ https://www.ncbi.nlm.nih.gov/pubmed/34162999 http://dx.doi.org/10.1038/s42003-021-02333-5 |
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