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...

Full description

Bibliographic Details
Main Authors: Patrícia Santos-Oliveira, António Correia, Tiago Rodrigues, Teresa M Ribeiro-Rodrigues, Paulo Matafome, Juan Carlos Rodríguez-Manzaneque, Raquel Seiça, Henrique Girão, Rui D M Travasso
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-08-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1004436
_version_ 1818581894554451968
author Patrícia Santos-Oliveira
António Correia
Tiago Rodrigues
Teresa M Ribeiro-Rodrigues
Paulo Matafome
Juan Carlos Rodríguez-Manzaneque
Raquel Seiça
Henrique Girão
Rui D M Travasso
author_facet Patrícia Santos-Oliveira
António Correia
Tiago Rodrigues
Teresa M Ribeiro-Rodrigues
Paulo Matafome
Juan Carlos Rodríguez-Manzaneque
Raquel Seiça
Henrique Girão
Rui D M Travasso
author_sort Patrícia Santos-Oliveira
collection DOAJ
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.
first_indexed 2024-12-16T07:40:45Z
format Article
id doaj.art-785524e953a24456b545e8b44265be31
institution Directory Open Access Journal
issn 1553-734X
1553-7358
language English
last_indexed 2024-12-16T07:40:45Z
publishDate 2015-08-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Computational Biology
spelling doaj.art-785524e953a24456b545e8b44265be312022-12-21T22:39:05ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582015-08-01118e100443610.1371/journal.pcbi.1004436The Force at the Tip--Modelling Tension and Proliferation in Sprouting Angiogenesis.Patrícia Santos-OliveiraAntónio CorreiaTiago RodriguesTeresa M Ribeiro-RodriguesPaulo MatafomeJuan Carlos Rodríguez-ManzanequeRaquel SeiçaHenrique GirãoRui D M TravassoSprouting 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.https://doi.org/10.1371/journal.pcbi.1004436
spellingShingle Patrícia Santos-Oliveira
António Correia
Tiago Rodrigues
Teresa M Ribeiro-Rodrigues
Paulo Matafome
Juan Carlos Rodríguez-Manzaneque
Raquel Seiça
Henrique Girão
Rui D M Travasso
The Force at the Tip--Modelling Tension and Proliferation in Sprouting Angiogenesis.
PLoS Computational Biology
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
url https://doi.org/10.1371/journal.pcbi.1004436
work_keys_str_mv AT patriciasantosoliveira theforceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT antoniocorreia theforceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT tiagorodrigues theforceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT teresamribeirorodrigues theforceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT paulomatafome theforceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT juancarlosrodriguezmanzaneque theforceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT raquelseica theforceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT henriquegirao theforceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT ruidmtravasso theforceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT patriciasantosoliveira forceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT antoniocorreia forceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT tiagorodrigues forceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT teresamribeirorodrigues forceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT paulomatafome forceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT juancarlosrodriguezmanzaneque forceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT raquelseica forceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT henriquegirao forceatthetipmodellingtensionandproliferationinsproutingangiogenesis
AT ruidmtravasso forceatthetipmodellingtensionandproliferationinsproutingangiogenesis