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Two-Layer Elastographic 3-D Traction Force Microscopy

Cellular traction force microscopy (TFM) requires knowledge of the mechanical properties of the substratum where the cells adhere to calculate cell-generated forces from measurements of substratum deformation. Polymer-based hydrogels are broadly used for TFM due to their linearly elastic behavior in...

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Autores principales: Álvarez-González, Begoña, Zhang, Shun, Gómez-González, Manuel, Meili, Ruedi, Firtel, Richard A., Lasheras, Juan C., del Álamo, Juan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225457/
https://www.ncbi.nlm.nih.gov/pubmed/28074837
http://dx.doi.org/10.1038/srep39315
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author Álvarez-González, Begoña
Zhang, Shun
Gómez-González, Manuel
Meili, Ruedi
Firtel, Richard A.
Lasheras, Juan C.
del Álamo, Juan C.
author_facet Álvarez-González, Begoña
Zhang, Shun
Gómez-González, Manuel
Meili, Ruedi
Firtel, Richard A.
Lasheras, Juan C.
del Álamo, Juan C.
author_sort Álvarez-González, Begoña
collection PubMed
description Cellular traction force microscopy (TFM) requires knowledge of the mechanical properties of the substratum where the cells adhere to calculate cell-generated forces from measurements of substratum deformation. Polymer-based hydrogels are broadly used for TFM due to their linearly elastic behavior in the range of measured deformations. However, the calculated stresses, particularly their spatial patterns, can be highly sensitive to the substratum’s Poisson’s ratio. We present two-layer elastographic TFM (2LETFM), a method that allows for simultaneously measuring the Poisson’s ratio of the substratum while also determining the cell-generated forces. The new method exploits the analytical solution of the elastostatic equation and deformation measurements from two layers of the substratum. We perform an in silico analysis of 2LETFM concluding that this technique is robust with respect to TFM experimental parameters, and remains accurate even for noisy measurement data. We also provide experimental proof of principle of 2LETFM by simultaneously measuring the stresses exerted by migrating Physarum amoeboae on the surface of polyacrylamide substrata, and the Poisson’s ratio of the substrata. The 2LETFM method could be generalized to concurrently determine the mechanical properties and cell-generated forces in more physiologically relevant extracellular environments, opening new possibilities to study cell-matrix interactions.
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spelling pubmed-52254572017-01-17 Two-Layer Elastographic 3-D Traction Force Microscopy Álvarez-González, Begoña Zhang, Shun Gómez-González, Manuel Meili, Ruedi Firtel, Richard A. Lasheras, Juan C. del Álamo, Juan C. Sci Rep Article Cellular traction force microscopy (TFM) requires knowledge of the mechanical properties of the substratum where the cells adhere to calculate cell-generated forces from measurements of substratum deformation. Polymer-based hydrogels are broadly used for TFM due to their linearly elastic behavior in the range of measured deformations. However, the calculated stresses, particularly their spatial patterns, can be highly sensitive to the substratum’s Poisson’s ratio. We present two-layer elastographic TFM (2LETFM), a method that allows for simultaneously measuring the Poisson’s ratio of the substratum while also determining the cell-generated forces. The new method exploits the analytical solution of the elastostatic equation and deformation measurements from two layers of the substratum. We perform an in silico analysis of 2LETFM concluding that this technique is robust with respect to TFM experimental parameters, and remains accurate even for noisy measurement data. We also provide experimental proof of principle of 2LETFM by simultaneously measuring the stresses exerted by migrating Physarum amoeboae on the surface of polyacrylamide substrata, and the Poisson’s ratio of the substrata. The 2LETFM method could be generalized to concurrently determine the mechanical properties and cell-generated forces in more physiologically relevant extracellular environments, opening new possibilities to study cell-matrix interactions. Nature Publishing Group 2017-01-11 /pmc/articles/PMC5225457/ /pubmed/28074837 http://dx.doi.org/10.1038/srep39315 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Álvarez-González, Begoña
Zhang, Shun
Gómez-González, Manuel
Meili, Ruedi
Firtel, Richard A.
Lasheras, Juan C.
del Álamo, Juan C.
Two-Layer Elastographic 3-D Traction Force Microscopy
title Two-Layer Elastographic 3-D Traction Force Microscopy
title_full Two-Layer Elastographic 3-D Traction Force Microscopy
title_fullStr Two-Layer Elastographic 3-D Traction Force Microscopy
title_full_unstemmed Two-Layer Elastographic 3-D Traction Force Microscopy
title_short Two-Layer Elastographic 3-D Traction Force Microscopy
title_sort two-layer elastographic 3-d traction force microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225457/
https://www.ncbi.nlm.nih.gov/pubmed/28074837
http://dx.doi.org/10.1038/srep39315
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