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...
Main Authors: | , , , , , |
---|---|
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 |
id |
doaj-aae3e70201884092903f013d537a71c9 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT nestorsepulveda collectivecellmotioninanepithelialsheetcanbequantitativelydescribedbyastochasticinteractingparticlemodel AT laurencepetitjean collectivecellmotioninanepithelialsheetcanbequantitativelydescribedbyastochasticinteractingparticlemodel AT oliviercochet collectivecellmotioninanepithelialsheetcanbequantitativelydescribedbyastochasticinteractingparticlemodel AT erwangraslandmongrain collectivecellmotioninanepithelialsheetcanbequantitativelydescribedbyastochasticinteractingparticlemodel AT pascalsilberzan collectivecellmotioninanepithelialsheetcanbequantitativelydescribedbyastochasticinteractingparticlemodel AT vincenthakim collectivecellmotioninanepithelialsheetcanbequantitativelydescribedbyastochasticinteractingparticlemodel |
_version_ |
1724876919454826496 |