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Leading-edge elongation by follower cell interruption in advancing epithelial cell sheets
Collective cell migration is seen in many developmental and pathological processes, such as morphogenesis, wound closure, and cancer metastasis. When a fish scale is detached and adhered to a substrate, epithelial keratocyte sheets crawl out from it, building a semicircular pattern. All the keratocy...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170137/ https://www.ncbi.nlm.nih.gov/pubmed/35476514 http://dx.doi.org/10.1073/pnas.2119903119 |
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author | Okimura, Chika Iwanaga, Misaki Sakurai, Tatsunari Ueno, Tasuku Urano, Yasuteru Iwadate, Yoshiaki |
author_facet | Okimura, Chika Iwanaga, Misaki Sakurai, Tatsunari Ueno, Tasuku Urano, Yasuteru Iwadate, Yoshiaki |
author_sort | Okimura, Chika |
collection | PubMed |
description | Collective cell migration is seen in many developmental and pathological processes, such as morphogenesis, wound closure, and cancer metastasis. When a fish scale is detached and adhered to a substrate, epithelial keratocyte sheets crawl out from it, building a semicircular pattern. All the keratocytes at the leading edge of the sheet have a single lamellipodium, and are interconnected with each other via actomyosin cables. The leading edge of the sheet becomes gradually longer as it crawls out from the scale, regardless of the cell-to-cell connections. In this study, we found leading-edge elongation to be realized by the interruption of follower cells into the leading edge. The follower cell and the two adjacent leader cells are first connected by newly emerging actomyosin cables. Then, the contractile forces along the cables bring the follower cell forward to make it a leader cell. Finally, the original cables between the two leader cells are stretched to tear by the interruption and the lamellipodium extension from the new leader cell. This unique actomyosin-cable reconnection between a follower cell and adjacent leaders offers insights into the mechanisms of collective cell migration. |
format | Online Article Text |
id | pubmed-9170137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-91701372022-10-27 Leading-edge elongation by follower cell interruption in advancing epithelial cell sheets Okimura, Chika Iwanaga, Misaki Sakurai, Tatsunari Ueno, Tasuku Urano, Yasuteru Iwadate, Yoshiaki Proc Natl Acad Sci U S A Biological Sciences Collective cell migration is seen in many developmental and pathological processes, such as morphogenesis, wound closure, and cancer metastasis. When a fish scale is detached and adhered to a substrate, epithelial keratocyte sheets crawl out from it, building a semicircular pattern. All the keratocytes at the leading edge of the sheet have a single lamellipodium, and are interconnected with each other via actomyosin cables. The leading edge of the sheet becomes gradually longer as it crawls out from the scale, regardless of the cell-to-cell connections. In this study, we found leading-edge elongation to be realized by the interruption of follower cells into the leading edge. The follower cell and the two adjacent leader cells are first connected by newly emerging actomyosin cables. Then, the contractile forces along the cables bring the follower cell forward to make it a leader cell. Finally, the original cables between the two leader cells are stretched to tear by the interruption and the lamellipodium extension from the new leader cell. This unique actomyosin-cable reconnection between a follower cell and adjacent leaders offers insights into the mechanisms of collective cell migration. National Academy of Sciences 2022-04-27 2022-05-03 /pmc/articles/PMC9170137/ /pubmed/35476514 http://dx.doi.org/10.1073/pnas.2119903119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Okimura, Chika Iwanaga, Misaki Sakurai, Tatsunari Ueno, Tasuku Urano, Yasuteru Iwadate, Yoshiaki Leading-edge elongation by follower cell interruption in advancing epithelial cell sheets |
title | Leading-edge elongation by follower cell interruption in advancing epithelial cell sheets |
title_full | Leading-edge elongation by follower cell interruption in advancing epithelial cell sheets |
title_fullStr | Leading-edge elongation by follower cell interruption in advancing epithelial cell sheets |
title_full_unstemmed | Leading-edge elongation by follower cell interruption in advancing epithelial cell sheets |
title_short | Leading-edge elongation by follower cell interruption in advancing epithelial cell sheets |
title_sort | leading-edge elongation by follower cell interruption in advancing epithelial cell sheets |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170137/ https://www.ncbi.nlm.nih.gov/pubmed/35476514 http://dx.doi.org/10.1073/pnas.2119903119 |
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