Collective cell motion in an epithelial sheet can be quantitatively described by a stochastic interacting particle model.

Modelling the displacement of thousands of cells that move in a collective way is required for the simulation and the theoretical analysis of various biological processes. Here, we tackle this question in the controlled setting where the motion of Madin-Darby Canine Kidney (MDCK) cells in a confluen...

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Main Authors: Néstor Sepúlveda, Laurence Petitjean, Olivier Cochet, Erwan Grasland-Mongrain, Pascal Silberzan, Vincent Hakim
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS Computational Biology
Online Access:http://europepmc.org/articles/PMC3591275?pdf=render
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spelling doaj-aae3e70201884092903f013d537a71c92020-11-25T02:19:18ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582013-01-0193e100294410.1371/journal.pcbi.1002944Collective cell motion in an epithelial sheet can be quantitatively described by a stochastic interacting particle model.Néstor SepúlvedaLaurence PetitjeanOlivier CochetErwan Grasland-MongrainPascal SilberzanVincent HakimModelling the displacement of thousands of cells that move in a collective way is required for the simulation and the theoretical analysis of various biological processes. Here, we tackle this question in the controlled setting where the motion of Madin-Darby Canine Kidney (MDCK) cells in a confluent epithelium is triggered by the unmasking of free surface. We develop a simple model in which cells are described as point particles with a dynamic based on the two premises that, first, cells move in a stochastic manner and, second, tend to adapt their motion to that of their neighbors. Detailed comparison to experimental data show that the model provides a quantitatively accurate description of cell motion in the epithelium bulk at early times. In addition, inclusion of model "leader" cells with modified characteristics, accounts for the digitated shape of the interface which develops over the subsequent hours, providing that leader cells invade free surface more easily than other cells and coordinate their motion with their followers. The previously-described progression of the epithelium border is reproduced by the model and quantitatively explained.http://europepmc.org/articles/PMC3591275?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Néstor Sepúlveda
Laurence Petitjean
Olivier Cochet
Erwan Grasland-Mongrain
Pascal Silberzan
Vincent Hakim
spellingShingle Néstor Sepúlveda
Laurence Petitjean
Olivier Cochet
Erwan Grasland-Mongrain
Pascal Silberzan
Vincent Hakim
Collective cell motion in an epithelial sheet can be quantitatively described by a stochastic interacting particle model.
PLoS Computational Biology
author_facet Néstor Sepúlveda
Laurence Petitjean
Olivier Cochet
Erwan Grasland-Mongrain
Pascal Silberzan
Vincent Hakim
author_sort Néstor Sepúlveda
title Collective cell motion in an epithelial sheet can be quantitatively described by a stochastic interacting particle model.
title_short Collective cell motion in an epithelial sheet can be quantitatively described by a stochastic interacting particle model.
title_full Collective cell motion in an epithelial sheet can be quantitatively described by a stochastic interacting particle model.
title_fullStr Collective cell motion in an epithelial sheet can be quantitatively described by a stochastic interacting particle model.
title_full_unstemmed Collective cell motion in an epithelial sheet can be quantitatively described by a stochastic interacting particle model.
title_sort collective cell motion in an epithelial sheet can be quantitatively described by a stochastic interacting particle model.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2013-01-01
description Modelling the displacement of thousands of cells that move in a collective way is required for the simulation and the theoretical analysis of various biological processes. Here, we tackle this question in the controlled setting where the motion of Madin-Darby Canine Kidney (MDCK) cells in a confluent epithelium is triggered by the unmasking of free surface. We develop a simple model in which cells are described as point particles with a dynamic based on the two premises that, first, cells move in a stochastic manner and, second, tend to adapt their motion to that of their neighbors. Detailed comparison to experimental data show that the model provides a quantitatively accurate description of cell motion in the epithelium bulk at early times. In addition, inclusion of model "leader" cells with modified characteristics, accounts for the digitated shape of the interface which develops over the subsequent hours, providing that leader cells invade free surface more easily than other cells and coordinate their motion with their followers. The previously-described progression of the epithelium border is reproduced by the model and quantitatively explained.
url http://europepmc.org/articles/PMC3591275?pdf=render
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