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Epithelial invagination by a vertical telescoping cell movement in mammalian salivary glands and teeth
Epithelial bending is a fundamental process that shapes organs during development. Previously known mechanisms involve cells locally changing shape from columnar to wedge-shaped. Here we report a different mechanism that occurs without cell wedging. In mammalian salivary glands and teeth, we show th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217937/ https://www.ncbi.nlm.nih.gov/pubmed/32398639 http://dx.doi.org/10.1038/s41467-020-16247-z |
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author | Li, Jingjing Economou, Andrew D. Vacca, Barbara Green, Jeremy B. A. |
author_facet | Li, Jingjing Economou, Andrew D. Vacca, Barbara Green, Jeremy B. A. |
author_sort | Li, Jingjing |
collection | PubMed |
description | Epithelial bending is a fundamental process that shapes organs during development. Previously known mechanisms involve cells locally changing shape from columnar to wedge-shaped. Here we report a different mechanism that occurs without cell wedging. In mammalian salivary glands and teeth, we show that initial invagination occurs through coordinated vertical cell movement: cells towards the periphery of the placode move vertically upwards while their more central neighbours move downwards. Movement is achieved by active cell-on-cell migration: outer cells migrate with apical, centripetally polarised leading edge protrusions but remain attached to the basal lamina, depressing more central neighbours to “telescope” the epithelium downwards into underlying mesenchyme. Inhibiting protrusion formation by Arp2/3 protein blocks invagination. FGF and Hedgehog morphogen signals are required, with FGF providing a directional cue. These findings show that epithelial bending can be achieved by a morphogenetic mechanism of coordinated cell rearrangement quite distinct from previously recognised invagination processes. |
format | Online Article Text |
id | pubmed-7217937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72179372020-05-15 Epithelial invagination by a vertical telescoping cell movement in mammalian salivary glands and teeth Li, Jingjing Economou, Andrew D. Vacca, Barbara Green, Jeremy B. A. Nat Commun Article Epithelial bending is a fundamental process that shapes organs during development. Previously known mechanisms involve cells locally changing shape from columnar to wedge-shaped. Here we report a different mechanism that occurs without cell wedging. In mammalian salivary glands and teeth, we show that initial invagination occurs through coordinated vertical cell movement: cells towards the periphery of the placode move vertically upwards while their more central neighbours move downwards. Movement is achieved by active cell-on-cell migration: outer cells migrate with apical, centripetally polarised leading edge protrusions but remain attached to the basal lamina, depressing more central neighbours to “telescope” the epithelium downwards into underlying mesenchyme. Inhibiting protrusion formation by Arp2/3 protein blocks invagination. FGF and Hedgehog morphogen signals are required, with FGF providing a directional cue. These findings show that epithelial bending can be achieved by a morphogenetic mechanism of coordinated cell rearrangement quite distinct from previously recognised invagination processes. Nature Publishing Group UK 2020-05-12 /pmc/articles/PMC7217937/ /pubmed/32398639 http://dx.doi.org/10.1038/s41467-020-16247-z Text en © The Author(s) 2020 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/. |
spellingShingle | Article Li, Jingjing Economou, Andrew D. Vacca, Barbara Green, Jeremy B. A. Epithelial invagination by a vertical telescoping cell movement in mammalian salivary glands and teeth |
title | Epithelial invagination by a vertical telescoping cell movement in mammalian salivary glands and teeth |
title_full | Epithelial invagination by a vertical telescoping cell movement in mammalian salivary glands and teeth |
title_fullStr | Epithelial invagination by a vertical telescoping cell movement in mammalian salivary glands and teeth |
title_full_unstemmed | Epithelial invagination by a vertical telescoping cell movement in mammalian salivary glands and teeth |
title_short | Epithelial invagination by a vertical telescoping cell movement in mammalian salivary glands and teeth |
title_sort | epithelial invagination by a vertical telescoping cell movement in mammalian salivary glands and teeth |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217937/ https://www.ncbi.nlm.nih.gov/pubmed/32398639 http://dx.doi.org/10.1038/s41467-020-16247-z |
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