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Title: Collisions of deformable cells lead to collective migration

Abstract

Collective migration of eukaryotic cells plays a fundamental role in tissue growth, wound healing and immune response. The motion, arising spontaneously or in response to chemical and mechanical stimuli, is also important for understanding life-threatening pathologies, such as cancer and metastasis formation. We present a phase-field model to describe the movement of many self-organized, interacting cells. The model takes into account the main mechanisms of cell motility – acto-myosin dynamics, as well as substrate-mediated and cell-cell adhesion. It predicts that collective cell migration emerges spontaneously as a result of inelastic collisions between neighboring cells: collisions lead to a mutual alignment of the cell velocities and to the formation of coherently-moving multi-cellular clusters. Small cell-to-cell adhesion, in turn, reduces the propensity for large-scale collective migration, while higher adhesion leads to the formation of moving bands. Our study provides valuable insight into biological processes associated with collective cell motility.

Authors:
 [1];  [2];  [3]
  1. Technische Universitat Berlin (Germany). Inst. fur Theoretische Physik.
  2. Albert-Ludwigs-Universitat Freiburg (Germany). Physikalisches Institut; Institut Charles Sadron, Strasbourg Cedex (France)
  3. Argonne National Lab. (ANL), Argonne, IL (United States); Northwestern Univ., Evanston, IL (United States). Engineering Sciences and Applied Mathematics.
Publication Date:
Research Org.:
Argonne National Laboratory (ANL), Argonne, IL (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES); German Research Foundation (DFG); USDOE Office of Science - Office of Basic Energy Sciences - Materials Sciences and Engineering Division
OSTI Identifier:
1201501
Alternate Identifier(s):
OSTI ID: 1392522
Grant/Contract Number:  
AC02-06CH11357
Resource Type:
Accepted Manuscript
Journal Name:
Scientific Reports
Additional Journal Information:
Journal Volume: 5; Journal Issue: 1; Journal ID: ISSN 2045-2322
Publisher:
Nature Publishing Group
Country of Publication:
United States
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES; Computational biophysics; biomaterials - cells

Citation Formats

Löber, Jakob, Ziebert, Falko, and Aranson, Igor S. Collisions of deformable cells lead to collective migration. United States: N. p., 2015. Web. doi:10.1038/srep09172.
Löber, Jakob, Ziebert, Falko, & Aranson, Igor S. Collisions of deformable cells lead to collective migration. United States. https://doi.org/10.1038/srep09172
Löber, Jakob, Ziebert, Falko, and Aranson, Igor S. Tue . "Collisions of deformable cells lead to collective migration". United States. https://doi.org/10.1038/srep09172. https://www.osti.gov/servlets/purl/1201501.
@article{osti_1201501,
title = {Collisions of deformable cells lead to collective migration},
author = {Löber, Jakob and Ziebert, Falko and Aranson, Igor S.},
abstractNote = {Collective migration of eukaryotic cells plays a fundamental role in tissue growth, wound healing and immune response. The motion, arising spontaneously or in response to chemical and mechanical stimuli, is also important for understanding life-threatening pathologies, such as cancer and metastasis formation. We present a phase-field model to describe the movement of many self-organized, interacting cells. The model takes into account the main mechanisms of cell motility – acto-myosin dynamics, as well as substrate-mediated and cell-cell adhesion. It predicts that collective cell migration emerges spontaneously as a result of inelastic collisions between neighboring cells: collisions lead to a mutual alignment of the cell velocities and to the formation of coherently-moving multi-cellular clusters. Small cell-to-cell adhesion, in turn, reduces the propensity for large-scale collective migration, while higher adhesion leads to the formation of moving bands. Our study provides valuable insight into biological processes associated with collective cell motility.},
doi = {10.1038/srep09172},
journal = {Scientific Reports},
number = 1,
volume = 5,
place = {United States},
year = {Tue Mar 17 00:00:00 EDT 2015},
month = {Tue Mar 17 00:00:00 EDT 2015}
}

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Cited by: 110 works
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