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Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo
During embryonic development, regeneration, and homeostasis, cells have to migrate and physically integrate into the target tissues where they ultimately execute their function. While much is known about the biochemical pathways driving cell migration in vivo, we are only beginning to understand the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616887/ https://www.ncbi.nlm.nih.gov/pubmed/36307428 http://dx.doi.org/10.1038/s41467-022-34165-0 |
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author | Ventura, Guilherme Amiri, Aboutaleb Thiagarajan, Raghavan Tolonen, Mari Doostmohammadi, Amin Sedzinski, Jakub |
author_facet | Ventura, Guilherme Amiri, Aboutaleb Thiagarajan, Raghavan Tolonen, Mari Doostmohammadi, Amin Sedzinski, Jakub |
author_sort | Ventura, Guilherme |
collection | PubMed |
description | During embryonic development, regeneration, and homeostasis, cells have to migrate and physically integrate into the target tissues where they ultimately execute their function. While much is known about the biochemical pathways driving cell migration in vivo, we are only beginning to understand the mechanical interplay between migrating cells and their surrounding tissue. Here, we reveal that multiciliated cell precursors in the Xenopus embryo use filopodia to pull at the vertices of the overlying epithelial sheet. This pulling is effectively used to sense vertex stiffness and identify the preferred positions for cell integration into the tissue. Notably, we find that pulling forces equip multiciliated cells with the ability to remodel the epithelial junctions of the neighboring cells, enabling them to generate a permissive environment that facilitates integration. Our findings reveal the intricate physical crosstalk at the cell-tissue interface and uncover previously unknown functions for mechanical forces in orchestrating cell integration. |
format | Online Article Text |
id | pubmed-9616887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96168872022-10-30 Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo Ventura, Guilherme Amiri, Aboutaleb Thiagarajan, Raghavan Tolonen, Mari Doostmohammadi, Amin Sedzinski, Jakub Nat Commun Article During embryonic development, regeneration, and homeostasis, cells have to migrate and physically integrate into the target tissues where they ultimately execute their function. While much is known about the biochemical pathways driving cell migration in vivo, we are only beginning to understand the mechanical interplay between migrating cells and their surrounding tissue. Here, we reveal that multiciliated cell precursors in the Xenopus embryo use filopodia to pull at the vertices of the overlying epithelial sheet. This pulling is effectively used to sense vertex stiffness and identify the preferred positions for cell integration into the tissue. Notably, we find that pulling forces equip multiciliated cells with the ability to remodel the epithelial junctions of the neighboring cells, enabling them to generate a permissive environment that facilitates integration. Our findings reveal the intricate physical crosstalk at the cell-tissue interface and uncover previously unknown functions for mechanical forces in orchestrating cell integration. Nature Publishing Group UK 2022-10-28 /pmc/articles/PMC9616887/ /pubmed/36307428 http://dx.doi.org/10.1038/s41467-022-34165-0 Text en © The Author(s) 2022 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 Ventura, Guilherme Amiri, Aboutaleb Thiagarajan, Raghavan Tolonen, Mari Doostmohammadi, Amin Sedzinski, Jakub Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo |
title | Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo |
title_full | Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo |
title_fullStr | Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo |
title_full_unstemmed | Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo |
title_short | Multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo |
title_sort | multiciliated cells use filopodia to probe tissue mechanics during epithelial integration in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616887/ https://www.ncbi.nlm.nih.gov/pubmed/36307428 http://dx.doi.org/10.1038/s41467-022-34165-0 |
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