High resolution, large deformation 3D traction force microscopy.

Traction Force Microscopy (TFM) is a powerful approach for quantifying cell-material interactions that over the last two decades has contributed significantly to our understanding of cellular mechanosensing and mechanotransduction. In addition, recent advances in three-dimensional (3D) imaging and t...

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Main Authors: Jennet Toyjanova, Eyal Bar-Kochba, Cristina López-Fagundo, Jonathan Reichner, Diane Hoffman-Kim, Christian Franck
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3989172?pdf=render
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spelling doaj-ccb271acc1254815b5b012d3b63b96612020-11-25T02:32:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0194e9097610.1371/journal.pone.0090976High resolution, large deformation 3D traction force microscopy.Jennet ToyjanovaEyal Bar-KochbaCristina López-FagundoJonathan ReichnerDiane Hoffman-KimChristian FranckTraction Force Microscopy (TFM) is a powerful approach for quantifying cell-material interactions that over the last two decades has contributed significantly to our understanding of cellular mechanosensing and mechanotransduction. In addition, recent advances in three-dimensional (3D) imaging and traction force analysis (3D TFM) have highlighted the significance of the third dimension in influencing various cellular processes. Yet irrespective of dimensionality, almost all TFM approaches have relied on a linear elastic theory framework to calculate cell surface tractions. Here we present a new high resolution 3D TFM algorithm which utilizes a large deformation formulation to quantify cellular displacement fields with unprecedented resolution. The results feature some of the first experimental evidence that cells are indeed capable of exerting large material deformations, which require the formulation of a new theoretical TFM framework to accurately calculate the traction forces. Based on our previous 3D TFM technique, we reformulate our approach to accurately account for large material deformation and quantitatively contrast and compare both linear and large deformation frameworks as a function of the applied cell deformation. Particular attention is paid in estimating the accuracy penalty associated with utilizing a traditional linear elastic approach in the presence of large deformation gradients.http://europepmc.org/articles/PMC3989172?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jennet Toyjanova
Eyal Bar-Kochba
Cristina López-Fagundo
Jonathan Reichner
Diane Hoffman-Kim
Christian Franck
spellingShingle Jennet Toyjanova
Eyal Bar-Kochba
Cristina López-Fagundo
Jonathan Reichner
Diane Hoffman-Kim
Christian Franck
High resolution, large deformation 3D traction force microscopy.
PLoS ONE
author_facet Jennet Toyjanova
Eyal Bar-Kochba
Cristina López-Fagundo
Jonathan Reichner
Diane Hoffman-Kim
Christian Franck
author_sort Jennet Toyjanova
title High resolution, large deformation 3D traction force microscopy.
title_short High resolution, large deformation 3D traction force microscopy.
title_full High resolution, large deformation 3D traction force microscopy.
title_fullStr High resolution, large deformation 3D traction force microscopy.
title_full_unstemmed High resolution, large deformation 3D traction force microscopy.
title_sort high resolution, large deformation 3d traction force microscopy.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Traction Force Microscopy (TFM) is a powerful approach for quantifying cell-material interactions that over the last two decades has contributed significantly to our understanding of cellular mechanosensing and mechanotransduction. In addition, recent advances in three-dimensional (3D) imaging and traction force analysis (3D TFM) have highlighted the significance of the third dimension in influencing various cellular processes. Yet irrespective of dimensionality, almost all TFM approaches have relied on a linear elastic theory framework to calculate cell surface tractions. Here we present a new high resolution 3D TFM algorithm which utilizes a large deformation formulation to quantify cellular displacement fields with unprecedented resolution. The results feature some of the first experimental evidence that cells are indeed capable of exerting large material deformations, which require the formulation of a new theoretical TFM framework to accurately calculate the traction forces. Based on our previous 3D TFM technique, we reformulate our approach to accurately account for large material deformation and quantitatively contrast and compare both linear and large deformation frameworks as a function of the applied cell deformation. Particular attention is paid in estimating the accuracy penalty associated with utilizing a traditional linear elastic approach in the presence of large deformation gradients.
url http://europepmc.org/articles/PMC3989172?pdf=render
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AT cristinalopezfagundo highresolutionlargedeformation3dtractionforcemicroscopy
AT jonathanreichner highresolutionlargedeformation3dtractionforcemicroscopy
AT dianehoffmankim highresolutionlargedeformation3dtractionforcemicroscopy
AT christianfranck highresolutionlargedeformation3dtractionforcemicroscopy
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