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Quantifying tissue growth, shape and collision via continuum models and Bayesian inference

Although tissues are usually studied in isolation, this situation rarely occurs in biology, as cells, tissues and organs coexist and interact across scales to determine both shape and function. Here, we take a quantitative approach combining data from recent experiments, mathematical modelling and B...

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Detalles Bibliográficos
Autores principales: Falcó, Carles, Cohen, Daniel J., Carrillo, José A., Baker, Ruth E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354467/
https://www.ncbi.nlm.nih.gov/pubmed/37464804
http://dx.doi.org/10.1098/rsif.2023.0184
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author Falcó, Carles
Cohen, Daniel J.
Carrillo, José A.
Baker, Ruth E.
author_facet Falcó, Carles
Cohen, Daniel J.
Carrillo, José A.
Baker, Ruth E.
author_sort Falcó, Carles
collection PubMed
description Although tissues are usually studied in isolation, this situation rarely occurs in biology, as cells, tissues and organs coexist and interact across scales to determine both shape and function. Here, we take a quantitative approach combining data from recent experiments, mathematical modelling and Bayesian parameter inference, to describe the self-assembly of multiple epithelial sheets by growth and collision. We use two simple and well-studied continuum models, where cells move either randomly or following population pressure gradients. After suitable calibration, both models prove to be practically identifiable, and can reproduce the main features of single tissue expansions. However, our findings reveal that whenever tissue–tissue interactions become relevant, the random motion assumption can lead to unrealistic behaviour. Under this setting, a model accounting for population pressure from different cell populations is more appropriate and shows a better agreement with experimental measurements. Finally, we discuss how tissue shape and pressure affect multi-tissue collisions. Our work thus provides a systematic approach to quantify and predict complex tissue configurations with applications in the design of tissue composites and more generally in tissue engineering.
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spelling pubmed-103544672023-07-20 Quantifying tissue growth, shape and collision via continuum models and Bayesian inference Falcó, Carles Cohen, Daniel J. Carrillo, José A. Baker, Ruth E. J R Soc Interface Life Sciences–Mathematics interface Although tissues are usually studied in isolation, this situation rarely occurs in biology, as cells, tissues and organs coexist and interact across scales to determine both shape and function. Here, we take a quantitative approach combining data from recent experiments, mathematical modelling and Bayesian parameter inference, to describe the self-assembly of multiple epithelial sheets by growth and collision. We use two simple and well-studied continuum models, where cells move either randomly or following population pressure gradients. After suitable calibration, both models prove to be practically identifiable, and can reproduce the main features of single tissue expansions. However, our findings reveal that whenever tissue–tissue interactions become relevant, the random motion assumption can lead to unrealistic behaviour. Under this setting, a model accounting for population pressure from different cell populations is more appropriate and shows a better agreement with experimental measurements. Finally, we discuss how tissue shape and pressure affect multi-tissue collisions. Our work thus provides a systematic approach to quantify and predict complex tissue configurations with applications in the design of tissue composites and more generally in tissue engineering. The Royal Society 2023-07-19 /pmc/articles/PMC10354467/ /pubmed/37464804 http://dx.doi.org/10.1098/rsif.2023.0184 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Life Sciences–Mathematics interface
Falcó, Carles
Cohen, Daniel J.
Carrillo, José A.
Baker, Ruth E.
Quantifying tissue growth, shape and collision via continuum models and Bayesian inference
title Quantifying tissue growth, shape and collision via continuum models and Bayesian inference
title_full Quantifying tissue growth, shape and collision via continuum models and Bayesian inference
title_fullStr Quantifying tissue growth, shape and collision via continuum models and Bayesian inference
title_full_unstemmed Quantifying tissue growth, shape and collision via continuum models and Bayesian inference
title_short Quantifying tissue growth, shape and collision via continuum models and Bayesian inference
title_sort quantifying tissue growth, shape and collision via continuum models and bayesian inference
topic Life Sciences–Mathematics interface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354467/
https://www.ncbi.nlm.nih.gov/pubmed/37464804
http://dx.doi.org/10.1098/rsif.2023.0184
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