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The Force at the Tip - Modelling Tension and Proliferation in Sprouting Angiogenesis
Sprouting angiogenesis, where new blood vessels grow from pre-existing ones, is a complex process where biochemical and mechanical signals regulate endothelial cell proliferation and movement. Therefore, a mathematical description of sprouting angiogenesis has to take into consideration biological s...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527825/ https://www.ncbi.nlm.nih.gov/pubmed/26248210 http://dx.doi.org/10.1371/journal.pcbi.1004436 |
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author | Santos-Oliveira, Patrícia Correia, António Rodrigues, Tiago Ribeiro-Rodrigues, Teresa M Matafome, Paulo Rodríguez-Manzaneque, Juan Carlos Seiça, Raquel Girão, Henrique Travasso, Rui D. M. |
author_facet | Santos-Oliveira, Patrícia Correia, António Rodrigues, Tiago Ribeiro-Rodrigues, Teresa M Matafome, Paulo Rodríguez-Manzaneque, Juan Carlos Seiça, Raquel Girão, Henrique Travasso, Rui D. M. |
author_sort | Santos-Oliveira, Patrícia |
collection | PubMed |
description | Sprouting angiogenesis, where new blood vessels grow from pre-existing ones, is a complex process where biochemical and mechanical signals regulate endothelial cell proliferation and movement. Therefore, a mathematical description of sprouting angiogenesis has to take into consideration biological signals as well as relevant physical processes, in particular the mechanical interplay between adjacent endothelial cells and the extracellular microenvironment. In this work, we introduce the first phase-field continuous model of sprouting angiogenesis capable of predicting sprout morphology as a function of the elastic properties of the tissues and the traction forces exerted by the cells. The model is very compact, only consisting of three coupled partial differential equations, and has the clear advantage of a reduced number of parameters. This model allows us to describe sprout growth as a function of the cell-cell adhesion forces and the traction force exerted by the sprout tip cell. In the absence of proliferation, we observe that the sprout either achieves a maximum length or, when the traction and adhesion are very large, it breaks. Endothelial cell proliferation alters significantly sprout morphology, and we explore how different types of endothelial cell proliferation regulation are able to determine the shape of the growing sprout. The largest region in parameter space with well formed long and straight sprouts is obtained always when the proliferation is triggered by endothelial cell strain and its rate grows with angiogenic factor concentration. We conclude that in this scenario the tip cell has the role of creating a tension in the cells that follow its lead. On those first stalk cells, this tension produces strain and/or empty spaces, inevitably triggering cell proliferation. The new cells occupy the space behind the tip, the tension decreases, and the process restarts. Our results highlight the ability of mathematical models to suggest relevant hypotheses with respect to the role of forces in sprouting, hence underlining the necessary collaboration between modelling and molecular biology techniques to improve the current state-of-the-art. |
format | Online Article Text |
id | pubmed-4527825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45278252015-08-12 The Force at the Tip - Modelling Tension and Proliferation in Sprouting Angiogenesis Santos-Oliveira, Patrícia Correia, António Rodrigues, Tiago Ribeiro-Rodrigues, Teresa M Matafome, Paulo Rodríguez-Manzaneque, Juan Carlos Seiça, Raquel Girão, Henrique Travasso, Rui D. M. PLoS Comput Biol Research Article Sprouting angiogenesis, where new blood vessels grow from pre-existing ones, is a complex process where biochemical and mechanical signals regulate endothelial cell proliferation and movement. Therefore, a mathematical description of sprouting angiogenesis has to take into consideration biological signals as well as relevant physical processes, in particular the mechanical interplay between adjacent endothelial cells and the extracellular microenvironment. In this work, we introduce the first phase-field continuous model of sprouting angiogenesis capable of predicting sprout morphology as a function of the elastic properties of the tissues and the traction forces exerted by the cells. The model is very compact, only consisting of three coupled partial differential equations, and has the clear advantage of a reduced number of parameters. This model allows us to describe sprout growth as a function of the cell-cell adhesion forces and the traction force exerted by the sprout tip cell. In the absence of proliferation, we observe that the sprout either achieves a maximum length or, when the traction and adhesion are very large, it breaks. Endothelial cell proliferation alters significantly sprout morphology, and we explore how different types of endothelial cell proliferation regulation are able to determine the shape of the growing sprout. The largest region in parameter space with well formed long and straight sprouts is obtained always when the proliferation is triggered by endothelial cell strain and its rate grows with angiogenic factor concentration. We conclude that in this scenario the tip cell has the role of creating a tension in the cells that follow its lead. On those first stalk cells, this tension produces strain and/or empty spaces, inevitably triggering cell proliferation. The new cells occupy the space behind the tip, the tension decreases, and the process restarts. Our results highlight the ability of mathematical models to suggest relevant hypotheses with respect to the role of forces in sprouting, hence underlining the necessary collaboration between modelling and molecular biology techniques to improve the current state-of-the-art. Public Library of Science 2015-08-06 /pmc/articles/PMC4527825/ /pubmed/26248210 http://dx.doi.org/10.1371/journal.pcbi.1004436 Text en © 2015 Santos-Oliveira et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited. |
spellingShingle | Research Article Santos-Oliveira, Patrícia Correia, António Rodrigues, Tiago Ribeiro-Rodrigues, Teresa M Matafome, Paulo Rodríguez-Manzaneque, Juan Carlos Seiça, Raquel Girão, Henrique Travasso, Rui D. M. The Force at the Tip - Modelling Tension and Proliferation in Sprouting Angiogenesis |
title | The Force at the Tip - Modelling Tension and Proliferation in Sprouting Angiogenesis |
title_full | The Force at the Tip - Modelling Tension and Proliferation in Sprouting Angiogenesis |
title_fullStr | The Force at the Tip - Modelling Tension and Proliferation in Sprouting Angiogenesis |
title_full_unstemmed | The Force at the Tip - Modelling Tension and Proliferation in Sprouting Angiogenesis |
title_short | The Force at the Tip - Modelling Tension and Proliferation in Sprouting Angiogenesis |
title_sort | force at the tip - modelling tension and proliferation in sprouting angiogenesis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527825/ https://www.ncbi.nlm.nih.gov/pubmed/26248210 http://dx.doi.org/10.1371/journal.pcbi.1004436 |
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