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Three-dimensional vertex model for simulating multicellular morphogenesis

During morphogenesis, various cellular activities are spatiotemporally coordinated on the protein regulatory background to construct the complicated, three-dimensional (3D) structures of organs. Computational simulations using 3D vertex models have been the focus of efforts to approach the mechanism...

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Detalles Bibliográficos
Autores principales: Okuda, Satoru, Inoue, Yasuhiro, Adachi, Taiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society of Japan (BSJ) 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736843/
https://www.ncbi.nlm.nih.gov/pubmed/27493850
http://dx.doi.org/10.2142/biophysico.12.0_13
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author Okuda, Satoru
Inoue, Yasuhiro
Adachi, Taiji
author_facet Okuda, Satoru
Inoue, Yasuhiro
Adachi, Taiji
author_sort Okuda, Satoru
collection PubMed
description During morphogenesis, various cellular activities are spatiotemporally coordinated on the protein regulatory background to construct the complicated, three-dimensional (3D) structures of organs. Computational simulations using 3D vertex models have been the focus of efforts to approach the mechanisms underlying 3D multicellular constructions, such as dynamics of the 3D monolayer or multilayer cell sheet like epithelia as well as the 3D compacted cell aggregate, including dynamic changes in layer structures. 3D vertex models enable the quantitative simulation of multicellular morphogenesis on the basis of single-cell mechanics, with complete control of various cellular activities such as cell contraction, growth, rearrangement, division, and death. This review describes the general use of the 3D vertex model, along with its applications to several simplified problems of developmental phenomena.
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spelling pubmed-47368432016-08-04 Three-dimensional vertex model for simulating multicellular morphogenesis Okuda, Satoru Inoue, Yasuhiro Adachi, Taiji Biophys Physicobiol Review Article During morphogenesis, various cellular activities are spatiotemporally coordinated on the protein regulatory background to construct the complicated, three-dimensional (3D) structures of organs. Computational simulations using 3D vertex models have been the focus of efforts to approach the mechanisms underlying 3D multicellular constructions, such as dynamics of the 3D monolayer or multilayer cell sheet like epithelia as well as the 3D compacted cell aggregate, including dynamic changes in layer structures. 3D vertex models enable the quantitative simulation of multicellular morphogenesis on the basis of single-cell mechanics, with complete control of various cellular activities such as cell contraction, growth, rearrangement, division, and death. This review describes the general use of the 3D vertex model, along with its applications to several simplified problems of developmental phenomena. The Biophysical Society of Japan (BSJ) 2015-08-18 /pmc/articles/PMC4736843/ /pubmed/27493850 http://dx.doi.org/10.2142/biophysico.12.0_13 Text en 2015 © The Biophysical Society of Japan This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Okuda, Satoru
Inoue, Yasuhiro
Adachi, Taiji
Three-dimensional vertex model for simulating multicellular morphogenesis
title Three-dimensional vertex model for simulating multicellular morphogenesis
title_full Three-dimensional vertex model for simulating multicellular morphogenesis
title_fullStr Three-dimensional vertex model for simulating multicellular morphogenesis
title_full_unstemmed Three-dimensional vertex model for simulating multicellular morphogenesis
title_short Three-dimensional vertex model for simulating multicellular morphogenesis
title_sort three-dimensional vertex model for simulating multicellular morphogenesis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736843/
https://www.ncbi.nlm.nih.gov/pubmed/27493850
http://dx.doi.org/10.2142/biophysico.12.0_13
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