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A cell-based computational model of early embryogenesis coupling mechanical behaviour and gene regulation
The study of multicellular development is grounded in two complementary domains: cell biomechanics, which examines how physical forces shape the embryo, and genetic regulation and molecular signalling, which concern how cells determine their states and behaviours. Integrating both sides into a unifi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264012/ https://www.ncbi.nlm.nih.gov/pubmed/28112150 http://dx.doi.org/10.1038/ncomms13929 |
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author | Delile, Julien Herrmann, Matthieu Peyriéras, Nadine Doursat, René |
author_facet | Delile, Julien Herrmann, Matthieu Peyriéras, Nadine Doursat, René |
author_sort | Delile, Julien |
collection | PubMed |
description | The study of multicellular development is grounded in two complementary domains: cell biomechanics, which examines how physical forces shape the embryo, and genetic regulation and molecular signalling, which concern how cells determine their states and behaviours. Integrating both sides into a unified framework is crucial to fully understand the self-organized dynamics of morphogenesis. Here we introduce MecaGen, an integrative modelling platform enabling the hypothesis-driven simulation of these dual processes via the coupling between mechanical and chemical variables. Our approach relies upon a minimal ‘cell behaviour ontology' comprising mesenchymal and epithelial cells and their associated behaviours. MecaGen enables the specification and control of complex collective movements in 3D space through a biologically relevant gene regulatory network and parameter space exploration. Three case studies investigating pattern formation, epithelial differentiation and tissue tectonics in zebrafish early embryogenesis, the latter with quantitative comparison to live imaging data, demonstrate the validity and usefulness of our framework. |
format | Online Article Text |
id | pubmed-5264012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52640122017-02-03 A cell-based computational model of early embryogenesis coupling mechanical behaviour and gene regulation Delile, Julien Herrmann, Matthieu Peyriéras, Nadine Doursat, René Nat Commun Article The study of multicellular development is grounded in two complementary domains: cell biomechanics, which examines how physical forces shape the embryo, and genetic regulation and molecular signalling, which concern how cells determine their states and behaviours. Integrating both sides into a unified framework is crucial to fully understand the self-organized dynamics of morphogenesis. Here we introduce MecaGen, an integrative modelling platform enabling the hypothesis-driven simulation of these dual processes via the coupling between mechanical and chemical variables. Our approach relies upon a minimal ‘cell behaviour ontology' comprising mesenchymal and epithelial cells and their associated behaviours. MecaGen enables the specification and control of complex collective movements in 3D space through a biologically relevant gene regulatory network and parameter space exploration. Three case studies investigating pattern formation, epithelial differentiation and tissue tectonics in zebrafish early embryogenesis, the latter with quantitative comparison to live imaging data, demonstrate the validity and usefulness of our framework. Nature Publishing Group 2017-01-23 /pmc/articles/PMC5264012/ /pubmed/28112150 http://dx.doi.org/10.1038/ncomms13929 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Delile, Julien Herrmann, Matthieu Peyriéras, Nadine Doursat, René A cell-based computational model of early embryogenesis coupling mechanical behaviour and gene regulation |
title | A cell-based computational model of early embryogenesis coupling mechanical behaviour and gene regulation |
title_full | A cell-based computational model of early embryogenesis coupling mechanical behaviour and gene regulation |
title_fullStr | A cell-based computational model of early embryogenesis coupling mechanical behaviour and gene regulation |
title_full_unstemmed | A cell-based computational model of early embryogenesis coupling mechanical behaviour and gene regulation |
title_short | A cell-based computational model of early embryogenesis coupling mechanical behaviour and gene regulation |
title_sort | cell-based computational model of early embryogenesis coupling mechanical behaviour and gene regulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264012/ https://www.ncbi.nlm.nih.gov/pubmed/28112150 http://dx.doi.org/10.1038/ncomms13929 |
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