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

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 co...

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Autores principales: Schnyder, Simon K., Molina, John J., Tanaka, Yuki, Yamamoto, Ryoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507894/
https://www.ncbi.nlm.nih.gov/pubmed/28701766
http://dx.doi.org/10.1038/s41598-017-05321-0
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author Schnyder, Simon K.
Molina, John J.
Tanaka, Yuki
Yamamoto, Ryoichi
author_facet Schnyder, Simon K.
Molina, John J.
Tanaka, Yuki
Yamamoto, Ryoichi
author_sort Schnyder, Simon K.
collection PubMed
description 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.
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spelling pubmed-55078942017-07-14 Collective motion of cells crawling on a substrate: roles of cell shape and contact inhibition Schnyder, Simon K. Molina, John J. Tanaka, Yuki Yamamoto, Ryoichi Sci Rep Article 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. Nature Publishing Group UK 2017-07-12 /pmc/articles/PMC5507894/ /pubmed/28701766 http://dx.doi.org/10.1038/s41598-017-05321-0 Text en © The Author(s) 2017 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
Schnyder, Simon K.
Molina, John J.
Tanaka, Yuki
Yamamoto, Ryoichi
Collective motion of cells crawling on a substrate: roles of cell shape and contact inhibition
title 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_short 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
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507894/
https://www.ncbi.nlm.nih.gov/pubmed/28701766
http://dx.doi.org/10.1038/s41598-017-05321-0
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