Matrix feedback enables diverse higher-order patterning of the extracellular matrix.

The higher-order patterning of extra-cellular matrix in normal and pathological tissues has profound consequences on tissue function. Whilst studies have documented both how fibroblasts create and maintain individual matrix fibers and how cell migration is altered by the fibers they interact with, a...

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Main Authors: Esther Wershof, Danielle Park, Robert P Jenkins, David J Barry, Erik Sahai, Paul A Bates
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-10-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1007251
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spelling doaj-c556d4006436430caeef4f9dbf2064102021-04-21T15:44:19ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582019-10-011510e100725110.1371/journal.pcbi.1007251Matrix feedback enables diverse higher-order patterning of the extracellular matrix.Esther WershofDanielle ParkRobert P JenkinsDavid J BarryErik SahaiPaul A BatesThe higher-order patterning of extra-cellular matrix in normal and pathological tissues has profound consequences on tissue function. Whilst studies have documented both how fibroblasts create and maintain individual matrix fibers and how cell migration is altered by the fibers they interact with, a model unifying these two aspects of tissue organization is lacking. Here we use computational modelling to understand the effect of this interconnectivity between fibroblasts and matrix at the mesoscale level. We created a unique adaptation to the Vicsek flocking model to include feedback from a second layer representing the matrix, and use experimentation to parameterize our model and validate model-driven hypotheses. Our two-layer model demonstrates that feedback between fibroblasts and matrix increases matrix diversity creating higher-order patterns. The model can quantitatively recapitulate matrix patterns of tissues in vivo. Cells follow matrix fibers irrespective of when the matrix fibers were deposited, resulting in feedback with the matrix acting as temporal 'memory' to collective behaviour, which creates diversity in topology. We also establish conditions under which matrix can be remodelled from one pattern to another. Our model elucidates how simple rules defining fibroblast-matrix interactions are sufficient to generate complex tissue patterns.https://doi.org/10.1371/journal.pcbi.1007251
collection DOAJ
language English
format Article
sources DOAJ
author Esther Wershof
Danielle Park
Robert P Jenkins
David J Barry
Erik Sahai
Paul A Bates
spellingShingle Esther Wershof
Danielle Park
Robert P Jenkins
David J Barry
Erik Sahai
Paul A Bates
Matrix feedback enables diverse higher-order patterning of the extracellular matrix.
PLoS Computational Biology
author_facet Esther Wershof
Danielle Park
Robert P Jenkins
David J Barry
Erik Sahai
Paul A Bates
author_sort Esther Wershof
title Matrix feedback enables diverse higher-order patterning of the extracellular matrix.
title_short Matrix feedback enables diverse higher-order patterning of the extracellular matrix.
title_full Matrix feedback enables diverse higher-order patterning of the extracellular matrix.
title_fullStr Matrix feedback enables diverse higher-order patterning of the extracellular matrix.
title_full_unstemmed Matrix feedback enables diverse higher-order patterning of the extracellular matrix.
title_sort matrix feedback enables diverse higher-order patterning of the extracellular matrix.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2019-10-01
description The higher-order patterning of extra-cellular matrix in normal and pathological tissues has profound consequences on tissue function. Whilst studies have documented both how fibroblasts create and maintain individual matrix fibers and how cell migration is altered by the fibers they interact with, a model unifying these two aspects of tissue organization is lacking. Here we use computational modelling to understand the effect of this interconnectivity between fibroblasts and matrix at the mesoscale level. We created a unique adaptation to the Vicsek flocking model to include feedback from a second layer representing the matrix, and use experimentation to parameterize our model and validate model-driven hypotheses. Our two-layer model demonstrates that feedback between fibroblasts and matrix increases matrix diversity creating higher-order patterns. The model can quantitatively recapitulate matrix patterns of tissues in vivo. Cells follow matrix fibers irrespective of when the matrix fibers were deposited, resulting in feedback with the matrix acting as temporal 'memory' to collective behaviour, which creates diversity in topology. We also establish conditions under which matrix can be remodelled from one pattern to another. Our model elucidates how simple rules defining fibroblast-matrix interactions are sufficient to generate complex tissue patterns.
url https://doi.org/10.1371/journal.pcbi.1007251
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