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Cell polarisation in a bulk-surface model can be driven by both classic and non-classic Turing instability
The GTPase Cdc42 is the master regulator of eukaryotic cell polarisation. During this process, the active form of Cdc42 is accumulated at a particular site on the cell membrane called the pole. It is believed that the accumulation of the active Cdc42 resulting in a pole is driven by a combination of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910310/ https://www.ncbi.nlm.nih.gov/pubmed/33637746 http://dx.doi.org/10.1038/s41540-021-00173-x |
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author | Borgqvist, Johannes Malik, Adam Lundholm, Carl Logg, Anders Gerlee, Philip Cvijovic, Marija |
author_facet | Borgqvist, Johannes Malik, Adam Lundholm, Carl Logg, Anders Gerlee, Philip Cvijovic, Marija |
author_sort | Borgqvist, Johannes |
collection | PubMed |
description | The GTPase Cdc42 is the master regulator of eukaryotic cell polarisation. During this process, the active form of Cdc42 is accumulated at a particular site on the cell membrane called the pole. It is believed that the accumulation of the active Cdc42 resulting in a pole is driven by a combination of activation–inactivation reactions and diffusion. It has been proposed using mathematical modelling that this is the result of diffusion-driven instability, originally proposed by Alan Turing. In this study, we developed, analysed and validated a 3D bulk-surface model of the dynamics of Cdc42. We show that the model can undergo both classic and non-classic Turing instability by deriving necessary conditions for which this occurs and conclude that the non-classic case can be viewed as a limit case of the classic case of diffusion-driven instability. Using three-dimensional Spatio-temporal simulation we predicted pole size and time to polarisation, suggesting that cell polarisation is mainly driven by the reaction strength parameter and that the size of the pole is determined by the relative diffusion. |
format | Online Article Text |
id | pubmed-7910310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79103102021-03-04 Cell polarisation in a bulk-surface model can be driven by both classic and non-classic Turing instability Borgqvist, Johannes Malik, Adam Lundholm, Carl Logg, Anders Gerlee, Philip Cvijovic, Marija NPJ Syst Biol Appl Article The GTPase Cdc42 is the master regulator of eukaryotic cell polarisation. During this process, the active form of Cdc42 is accumulated at a particular site on the cell membrane called the pole. It is believed that the accumulation of the active Cdc42 resulting in a pole is driven by a combination of activation–inactivation reactions and diffusion. It has been proposed using mathematical modelling that this is the result of diffusion-driven instability, originally proposed by Alan Turing. In this study, we developed, analysed and validated a 3D bulk-surface model of the dynamics of Cdc42. We show that the model can undergo both classic and non-classic Turing instability by deriving necessary conditions for which this occurs and conclude that the non-classic case can be viewed as a limit case of the classic case of diffusion-driven instability. Using three-dimensional Spatio-temporal simulation we predicted pole size and time to polarisation, suggesting that cell polarisation is mainly driven by the reaction strength parameter and that the size of the pole is determined by the relative diffusion. Nature Publishing Group UK 2021-02-26 /pmc/articles/PMC7910310/ /pubmed/33637746 http://dx.doi.org/10.1038/s41540-021-00173-x Text en © The Author(s) 2021 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 Borgqvist, Johannes Malik, Adam Lundholm, Carl Logg, Anders Gerlee, Philip Cvijovic, Marija Cell polarisation in a bulk-surface model can be driven by both classic and non-classic Turing instability |
title | Cell polarisation in a bulk-surface model can be driven by both classic and non-classic Turing instability |
title_full | Cell polarisation in a bulk-surface model can be driven by both classic and non-classic Turing instability |
title_fullStr | Cell polarisation in a bulk-surface model can be driven by both classic and non-classic Turing instability |
title_full_unstemmed | Cell polarisation in a bulk-surface model can be driven by both classic and non-classic Turing instability |
title_short | Cell polarisation in a bulk-surface model can be driven by both classic and non-classic Turing instability |
title_sort | cell polarisation in a bulk-surface model can be driven by both classic and non-classic turing instability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910310/ https://www.ncbi.nlm.nih.gov/pubmed/33637746 http://dx.doi.org/10.1038/s41540-021-00173-x |
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