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Tension Monitoring during Epithelial-to-Mesenchymal Transition Links the Switch of Phenotype to Expression of Moesin and Cadherins in NMuMG Cells

Structural alterations during epithelial-to-mesenchymal transition (EMT) pose a substantial challenge to the mechanical response of cells and are supposed to be key parameters for an increased malignancy during metastasis. Herein, we report that during EMT, apical tension of the epithelial cell line...

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Autores principales: Schneider, David, Baronsky, Thilo, Pietuch, Anna, Rother, Jan, Oelkers, Marieelen, Fichtner, Dagmar, Wedlich, Doris, Janshoff, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855076/
https://www.ncbi.nlm.nih.gov/pubmed/24339870
http://dx.doi.org/10.1371/journal.pone.0080068
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author Schneider, David
Baronsky, Thilo
Pietuch, Anna
Rother, Jan
Oelkers, Marieelen
Fichtner, Dagmar
Wedlich, Doris
Janshoff, Andreas
author_facet Schneider, David
Baronsky, Thilo
Pietuch, Anna
Rother, Jan
Oelkers, Marieelen
Fichtner, Dagmar
Wedlich, Doris
Janshoff, Andreas
author_sort Schneider, David
collection PubMed
description Structural alterations during epithelial-to-mesenchymal transition (EMT) pose a substantial challenge to the mechanical response of cells and are supposed to be key parameters for an increased malignancy during metastasis. Herein, we report that during EMT, apical tension of the epithelial cell line NMuMG is controlled by cell-cell contacts and the architecture of the underlying actin structures reflecting the mechanistic interplay between cellular structure and mechanics. Using force spectroscopy we find that tension in NMuMG cells slightly increases 24 h after EMT induction, whereas upon reaching the final mesenchymal-like state characterized by a complete loss of intercellular junctions and a concerted down-regulation of the adherens junction protein E-cadherin, the overall tension becomes similar to that of solitary adherent cells and fibroblasts. Interestingly, the contribution of the actin cytoskeleton on apical tension increases significantly upon EMT induction, most likely due to the formation of stable and highly contractile stress fibers which dominate the elastic properties of the cells after the transition. The structural alterations lead to the formation of single, highly motile cells rendering apical tension a good indicator for the cellular state during phenotype switching. In summary, our study paves the way towards a more profound understanding of cellular mechanics governing fundamental morphological programs such as the EMT.
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spelling pubmed-38550762013-12-11 Tension Monitoring during Epithelial-to-Mesenchymal Transition Links the Switch of Phenotype to Expression of Moesin and Cadherins in NMuMG Cells Schneider, David Baronsky, Thilo Pietuch, Anna Rother, Jan Oelkers, Marieelen Fichtner, Dagmar Wedlich, Doris Janshoff, Andreas PLoS One Research Article Structural alterations during epithelial-to-mesenchymal transition (EMT) pose a substantial challenge to the mechanical response of cells and are supposed to be key parameters for an increased malignancy during metastasis. Herein, we report that during EMT, apical tension of the epithelial cell line NMuMG is controlled by cell-cell contacts and the architecture of the underlying actin structures reflecting the mechanistic interplay between cellular structure and mechanics. Using force spectroscopy we find that tension in NMuMG cells slightly increases 24 h after EMT induction, whereas upon reaching the final mesenchymal-like state characterized by a complete loss of intercellular junctions and a concerted down-regulation of the adherens junction protein E-cadherin, the overall tension becomes similar to that of solitary adherent cells and fibroblasts. Interestingly, the contribution of the actin cytoskeleton on apical tension increases significantly upon EMT induction, most likely due to the formation of stable and highly contractile stress fibers which dominate the elastic properties of the cells after the transition. The structural alterations lead to the formation of single, highly motile cells rendering apical tension a good indicator for the cellular state during phenotype switching. In summary, our study paves the way towards a more profound understanding of cellular mechanics governing fundamental morphological programs such as the EMT. Public Library of Science 2013-12-05 /pmc/articles/PMC3855076/ /pubmed/24339870 http://dx.doi.org/10.1371/journal.pone.0080068 Text en © 2013 Schneider et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Schneider, David
Baronsky, Thilo
Pietuch, Anna
Rother, Jan
Oelkers, Marieelen
Fichtner, Dagmar
Wedlich, Doris
Janshoff, Andreas
Tension Monitoring during Epithelial-to-Mesenchymal Transition Links the Switch of Phenotype to Expression of Moesin and Cadherins in NMuMG Cells
title Tension Monitoring during Epithelial-to-Mesenchymal Transition Links the Switch of Phenotype to Expression of Moesin and Cadherins in NMuMG Cells
title_full Tension Monitoring during Epithelial-to-Mesenchymal Transition Links the Switch of Phenotype to Expression of Moesin and Cadherins in NMuMG Cells
title_fullStr Tension Monitoring during Epithelial-to-Mesenchymal Transition Links the Switch of Phenotype to Expression of Moesin and Cadherins in NMuMG Cells
title_full_unstemmed Tension Monitoring during Epithelial-to-Mesenchymal Transition Links the Switch of Phenotype to Expression of Moesin and Cadherins in NMuMG Cells
title_short Tension Monitoring during Epithelial-to-Mesenchymal Transition Links the Switch of Phenotype to Expression of Moesin and Cadherins in NMuMG Cells
title_sort tension monitoring during epithelial-to-mesenchymal transition links the switch of phenotype to expression of moesin and cadherins in nmumg cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855076/
https://www.ncbi.nlm.nih.gov/pubmed/24339870
http://dx.doi.org/10.1371/journal.pone.0080068
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