Collective motion of cells crawling on a substrate: roles of cell shape and contact inhibition

Abstract Contact inhibition plays a crucial role in cell motility, wound healing, and tumour formation. By mimicking the mechanical motion of cells crawling on a substrate, we constructed a minimal model of migrating cells that naturally gives rise to contact inhibition of locomotion (CIL). The mode...

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Autores principales: Simon K. Schnyder, John J. Molina, Yuki Tanaka, Ryoichi Yamamoto
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/8ffa6c5abc744bff8c0d4d2d6fca95dc
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spelling oai:doaj.org-article:8ffa6c5abc744bff8c0d4d2d6fca95dc2021-12-02T12:32:33ZCollective motion of cells crawling on a substrate: roles of cell shape and contact inhibition10.1038/s41598-017-05321-02045-2322https://doaj.org/article/8ffa6c5abc744bff8c0d4d2d6fca95dc2017-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-05321-0https://doaj.org/toc/2045-2322Abstract Contact inhibition plays a crucial role in cell motility, wound healing, and tumour formation. By mimicking the mechanical motion of cells crawling on a substrate, we constructed a minimal model of migrating cells that naturally gives rise to contact inhibition of locomotion (CIL). The model cell consists of two disks, a front disk (a pseudopod) and a back disk (cell body), which are connected by a finite extensible spring. Despite the simplicity of the model, the collective behaviour of the cells is highly non-trivial and depends on both the shape of the cells and whether CIL is enabled. Cells with a small front disk (i.e., a narrow pseudopod) form immobile colonies. In contrast, cells with a large front disk (e.g., a lamellipodium) exhibit coherent migration without any explicit alignment mechanism in the model. This result suggests that crawling cells often exhibit broad fronts because this helps facilitate alignment. After increasing the density, the cells develop density waves that propagate against the direction of cell migration and finally stop at higher densities.Simon K. SchnyderJohn J. MolinaYuki TanakaRyoichi YamamotoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-14 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Simon K. Schnyder
John J. Molina
Yuki Tanaka
Ryoichi Yamamoto
Collective motion of cells crawling on a substrate: roles of cell shape and contact inhibition
description Abstract Contact inhibition plays a crucial role in cell motility, wound healing, and tumour formation. By mimicking the mechanical motion of cells crawling on a substrate, we constructed a minimal model of migrating cells that naturally gives rise to contact inhibition of locomotion (CIL). The model cell consists of two disks, a front disk (a pseudopod) and a back disk (cell body), which are connected by a finite extensible spring. Despite the simplicity of the model, the collective behaviour of the cells is highly non-trivial and depends on both the shape of the cells and whether CIL is enabled. Cells with a small front disk (i.e., a narrow pseudopod) form immobile colonies. In contrast, cells with a large front disk (e.g., a lamellipodium) exhibit coherent migration without any explicit alignment mechanism in the model. This result suggests that crawling cells often exhibit broad fronts because this helps facilitate alignment. After increasing the density, the cells develop density waves that propagate against the direction of cell migration and finally stop at higher densities.
format article
author Simon K. Schnyder
John J. Molina
Yuki Tanaka
Ryoichi Yamamoto
author_facet Simon K. Schnyder
John J. Molina
Yuki Tanaka
Ryoichi Yamamoto
author_sort Simon K. Schnyder
title Collective motion of cells crawling on a substrate: roles of cell shape and contact inhibition
title_short Collective motion of cells crawling on a substrate: roles of cell shape and contact inhibition
title_full Collective motion of cells crawling on a substrate: roles of cell shape and contact inhibition
title_fullStr Collective motion of cells crawling on a substrate: roles of cell shape and contact inhibition
title_full_unstemmed Collective motion of cells crawling on a substrate: roles of cell shape and contact inhibition
title_sort collective motion of cells crawling on a substrate: roles of cell shape and contact inhibition
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/8ffa6c5abc744bff8c0d4d2d6fca95dc
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AT johnjmolina collectivemotionofcellscrawlingonasubstraterolesofcellshapeandcontactinhibition
AT yukitanaka collectivemotionofcellscrawlingonasubstraterolesofcellshapeandcontactinhibition
AT ryoichiyamamoto collectivemotionofcellscrawlingonasubstraterolesofcellshapeandcontactinhibition
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