An in vitro correlation of metastatic capacity and dual mechanostimulation.

Cells are under the influence of multiple forms of mechanical stimulation in vivo. For example, a cell is subjected to mechanical forces from tissue stiffness, shear and tensile stress and transient applied strain. Significant progress has been made in understanding the cellular mechanotransduction...

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Main Authors: Indrajyoti Indra, Alexander N Gasparski, Karen A Beningo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6241134?pdf=render
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spelling doaj-bb4e968fc2ee4fe3971d948a574c21672020-11-25T01:19:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-011311e020749010.1371/journal.pone.0207490An in vitro correlation of metastatic capacity and dual mechanostimulation.Indrajyoti IndraAlexander N GasparskiKaren A BeningoCells are under the influence of multiple forms of mechanical stimulation in vivo. For example, a cell is subjected to mechanical forces from tissue stiffness, shear and tensile stress and transient applied strain. Significant progress has been made in understanding the cellular mechanotransduction mechanisms in response to a single mechanical parameter. However, our knowledge of how a cell responds to multiple mechanical inputs is currently limited. In this study, we have tested the cellular response to the simultaneous application of two mechanical inputs: substrate compliance and transient tugging. Our results suggest that cells within a multicellular spheroid will restrict their response to a single mechanical input at a time and when provided with two mechanical inputs simultaneously, one will dominate. In normal and non-metastatic mammary epithelial cells, we found that they respond to applied stimulation and will override substrate compliance cues in favor of the applied mechanical stimulus. Surprisingly, however, metastatic mammary epithelial cells remain non-responsive to both mechanical cues. Our results suggest that, within our assay system, metastatic progression may involve the down-regulation of multiple mechanotransduction pathways.http://europepmc.org/articles/PMC6241134?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Indrajyoti Indra
Alexander N Gasparski
Karen A Beningo
spellingShingle Indrajyoti Indra
Alexander N Gasparski
Karen A Beningo
An in vitro correlation of metastatic capacity and dual mechanostimulation.
PLoS ONE
author_facet Indrajyoti Indra
Alexander N Gasparski
Karen A Beningo
author_sort Indrajyoti Indra
title An in vitro correlation of metastatic capacity and dual mechanostimulation.
title_short An in vitro correlation of metastatic capacity and dual mechanostimulation.
title_full An in vitro correlation of metastatic capacity and dual mechanostimulation.
title_fullStr An in vitro correlation of metastatic capacity and dual mechanostimulation.
title_full_unstemmed An in vitro correlation of metastatic capacity and dual mechanostimulation.
title_sort in vitro correlation of metastatic capacity and dual mechanostimulation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Cells are under the influence of multiple forms of mechanical stimulation in vivo. For example, a cell is subjected to mechanical forces from tissue stiffness, shear and tensile stress and transient applied strain. Significant progress has been made in understanding the cellular mechanotransduction mechanisms in response to a single mechanical parameter. However, our knowledge of how a cell responds to multiple mechanical inputs is currently limited. In this study, we have tested the cellular response to the simultaneous application of two mechanical inputs: substrate compliance and transient tugging. Our results suggest that cells within a multicellular spheroid will restrict their response to a single mechanical input at a time and when provided with two mechanical inputs simultaneously, one will dominate. In normal and non-metastatic mammary epithelial cells, we found that they respond to applied stimulation and will override substrate compliance cues in favor of the applied mechanical stimulus. Surprisingly, however, metastatic mammary epithelial cells remain non-responsive to both mechanical cues. Our results suggest that, within our assay system, metastatic progression may involve the down-regulation of multiple mechanotransduction pathways.
url http://europepmc.org/articles/PMC6241134?pdf=render
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