Hierarchical modeling of mechano-chemical dynamics of epithelial sheets across cells and tissue
Abstract Collective cell migration is a fundamental process in embryonic development and tissue homeostasis. This is a macroscopic population-level phenomenon that emerges across hierarchy from microscopic cell-cell interactions; however, the underlying mechanism remains unclear. Here, we addressed...
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2021-02-01
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doaj-a1f36c1201644cd48beb2191533f33ab2021-02-21T12:33:00ZengNature Publishing GroupScientific Reports2045-23222021-02-0111111510.1038/s41598-021-83396-6Hierarchical modeling of mechano-chemical dynamics of epithelial sheets across cells and tissueYoshifumi Asakura0Yohei Kondo1Kazuhiro Aoki2Honda Naoki3Laboratory of Theoretical Biology, Graduate School of Biostudies, Kyoto UniversityQuantitative Biology Research Group, Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural SciencesQuantitative Biology Research Group, Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural SciencesLaboratory of Theoretical Biology, Graduate School of Biostudies, Kyoto UniversityAbstract Collective cell migration is a fundamental process in embryonic development and tissue homeostasis. This is a macroscopic population-level phenomenon that emerges across hierarchy from microscopic cell-cell interactions; however, the underlying mechanism remains unclear. Here, we addressed this issue by focusing on epithelial collective cell migration, driven by the mechanical force regulated by chemical signals of traveling ERK activation waves, observed in wound healing. We propose a hierarchical mathematical framework for understanding how cells are orchestrated through mechanochemical cell-cell interaction. In this framework, we mathematically transformed a particle-based model at the cellular level into a continuum model at the tissue level. The continuum model described relationships between cell migration and mechanochemical variables, namely, ERK activity gradients, cell density, and velocity field, which could be compared with live-cell imaging data. Through numerical simulations, the continuum model recapitulated the ERK wave-induced collective cell migration in wound healing. We also numerically confirmed a consistency between these two models. Thus, our hierarchical approach offers a new theoretical platform to reveal a causality between macroscopic tissue-level and microscopic cellular-level phenomena. Furthermore, our model is also capable of deriving a theoretical insight on both of mechanical and chemical signals, in the causality of tissue and cellular dynamics.https://doi.org/10.1038/s41598-021-83396-6 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yoshifumi Asakura Yohei Kondo Kazuhiro Aoki Honda Naoki |
spellingShingle |
Yoshifumi Asakura Yohei Kondo Kazuhiro Aoki Honda Naoki Hierarchical modeling of mechano-chemical dynamics of epithelial sheets across cells and tissue Scientific Reports |
author_facet |
Yoshifumi Asakura Yohei Kondo Kazuhiro Aoki Honda Naoki |
author_sort |
Yoshifumi Asakura |
title |
Hierarchical modeling of mechano-chemical dynamics of epithelial sheets across cells and tissue |
title_short |
Hierarchical modeling of mechano-chemical dynamics of epithelial sheets across cells and tissue |
title_full |
Hierarchical modeling of mechano-chemical dynamics of epithelial sheets across cells and tissue |
title_fullStr |
Hierarchical modeling of mechano-chemical dynamics of epithelial sheets across cells and tissue |
title_full_unstemmed |
Hierarchical modeling of mechano-chemical dynamics of epithelial sheets across cells and tissue |
title_sort |
hierarchical modeling of mechano-chemical dynamics of epithelial sheets across cells and tissue |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-02-01 |
description |
Abstract Collective cell migration is a fundamental process in embryonic development and tissue homeostasis. This is a macroscopic population-level phenomenon that emerges across hierarchy from microscopic cell-cell interactions; however, the underlying mechanism remains unclear. Here, we addressed this issue by focusing on epithelial collective cell migration, driven by the mechanical force regulated by chemical signals of traveling ERK activation waves, observed in wound healing. We propose a hierarchical mathematical framework for understanding how cells are orchestrated through mechanochemical cell-cell interaction. In this framework, we mathematically transformed a particle-based model at the cellular level into a continuum model at the tissue level. The continuum model described relationships between cell migration and mechanochemical variables, namely, ERK activity gradients, cell density, and velocity field, which could be compared with live-cell imaging data. Through numerical simulations, the continuum model recapitulated the ERK wave-induced collective cell migration in wound healing. We also numerically confirmed a consistency between these two models. Thus, our hierarchical approach offers a new theoretical platform to reveal a causality between macroscopic tissue-level and microscopic cellular-level phenomena. Furthermore, our model is also capable of deriving a theoretical insight on both of mechanical and chemical signals, in the causality of tissue and cellular dynamics. |
url |
https://doi.org/10.1038/s41598-021-83396-6 |
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