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Border forces and friction control epithelial closure dynamics.


ABSTRACT: We study the closure dynamics of a large number of well-controlled circular apertures within an epithelial monolayer, where the collective cell migration responsible for epithelization is triggered by the removal of a spatial constraint rather than by scratching. Based on experimental observations, we propose a physical model that takes into account border forces, friction with the substrate, and tissue rheology. Border protrusive activity drives epithelization despite the presence of a contractile actomyosin cable at the periphery of the wound. The closure dynamics is quantified by an epithelization coefficient, defined as the ratio of protrusive stress to tissue-substrate friction, that allows classification of different phenotypes. The same analysis demonstrates a distinct signature for human cells bearing the oncogenic RasV12 mutation, demonstrating the potential of the approach to quantitatively characterize metastatic transformations.

SUBMITTER: Cochet-Escartin O 

PROVIDER: S-EPMC3907253 | biostudies-literature | 2014 Jan

REPOSITORIES: biostudies-literature

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Border forces and friction control epithelial closure dynamics.

Cochet-Escartin Olivier O   Ranft Jonas J   Silberzan Pascal P   Marcq Philippe P  

Biophysical journal 20140101 1


We study the closure dynamics of a large number of well-controlled circular apertures within an epithelial monolayer, where the collective cell migration responsible for epithelization is triggered by the removal of a spatial constraint rather than by scratching. Based on experimental observations, we propose a physical model that takes into account border forces, friction with the substrate, and tissue rheology. Border protrusive activity drives epithelization despite the presence of a contract  ...[more]

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