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Design and Construction of an Equibiaxial Cell Stretching System That Is Improved for Biochemical Analysis
We describe the design and validation of an equibiaxial stretching device in which cells are confined to regions of homogeneous strain. Using this device, we seek to overcome a significant limitation of existing equibiaxial stretching devices, in which strains are not homogeneous over the entire reg...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3953117/ https://www.ncbi.nlm.nih.gov/pubmed/24626190 http://dx.doi.org/10.1371/journal.pone.0090665 |
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author | Ursekar, Chaitanya Prashant Teo, Soo-Kng Hirata, Hiroaki Harada, Ichiro Chiam, Keng-Hwee Sawada, Yasuhiro |
author_facet | Ursekar, Chaitanya Prashant Teo, Soo-Kng Hirata, Hiroaki Harada, Ichiro Chiam, Keng-Hwee Sawada, Yasuhiro |
author_sort | Ursekar, Chaitanya Prashant |
collection | PubMed |
description | We describe the design and validation of an equibiaxial stretching device in which cells are confined to regions of homogeneous strain. Using this device, we seek to overcome a significant limitation of existing equibiaxial stretching devices, in which strains are not homogeneous over the entire region of cell culture. We cast PDMS in a mold to produce a membrane with a cylindrical wall incorporated in the center, which was used to confine cell monolayers to the central membrane region subjected to homogeneous equibiaxial strain. We demonstrated that the presence of the wall to hold the culture medium did not affect strain homogeneity over the majority of the culture surface and also showed that cells adhered well onto the PDMS membranes. We used our device in cyclic strain experiments and demonstrated strain-dependent changes in extracellular signal-regulated kinase (ERK) and tyrosine phosphorylation upon cell stretching. Furthermore, we examined cell responses to very small magnitudes of strain ranging from 1% to 6% and were able to observe a graduated increase in ERK phosphorylation in response to these strains. Collectively, we were able to study cellular biochemical response with a high degree of accuracy and sensitivity to fine changes in substrate strain. Because we have designed our device along the lines of existing equibiaxial stretching technologies, we believe that our innovations can be incorporated into existing systems. This device would provide a useful addition to the set of tools applied for in vitro studies of cell mechanobiology. |
format | Online Article Text |
id | pubmed-3953117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39531172014-03-18 Design and Construction of an Equibiaxial Cell Stretching System That Is Improved for Biochemical Analysis Ursekar, Chaitanya Prashant Teo, Soo-Kng Hirata, Hiroaki Harada, Ichiro Chiam, Keng-Hwee Sawada, Yasuhiro PLoS One Research Article We describe the design and validation of an equibiaxial stretching device in which cells are confined to regions of homogeneous strain. Using this device, we seek to overcome a significant limitation of existing equibiaxial stretching devices, in which strains are not homogeneous over the entire region of cell culture. We cast PDMS in a mold to produce a membrane with a cylindrical wall incorporated in the center, which was used to confine cell monolayers to the central membrane region subjected to homogeneous equibiaxial strain. We demonstrated that the presence of the wall to hold the culture medium did not affect strain homogeneity over the majority of the culture surface and also showed that cells adhered well onto the PDMS membranes. We used our device in cyclic strain experiments and demonstrated strain-dependent changes in extracellular signal-regulated kinase (ERK) and tyrosine phosphorylation upon cell stretching. Furthermore, we examined cell responses to very small magnitudes of strain ranging from 1% to 6% and were able to observe a graduated increase in ERK phosphorylation in response to these strains. Collectively, we were able to study cellular biochemical response with a high degree of accuracy and sensitivity to fine changes in substrate strain. Because we have designed our device along the lines of existing equibiaxial stretching technologies, we believe that our innovations can be incorporated into existing systems. This device would provide a useful addition to the set of tools applied for in vitro studies of cell mechanobiology. Public Library of Science 2014-03-13 /pmc/articles/PMC3953117/ /pubmed/24626190 http://dx.doi.org/10.1371/journal.pone.0090665 Text en © 2014 Ursekar 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 Ursekar, Chaitanya Prashant Teo, Soo-Kng Hirata, Hiroaki Harada, Ichiro Chiam, Keng-Hwee Sawada, Yasuhiro Design and Construction of an Equibiaxial Cell Stretching System That Is Improved for Biochemical Analysis |
title | Design and Construction of an Equibiaxial Cell Stretching System That Is Improved for Biochemical Analysis |
title_full | Design and Construction of an Equibiaxial Cell Stretching System That Is Improved for Biochemical Analysis |
title_fullStr | Design and Construction of an Equibiaxial Cell Stretching System That Is Improved for Biochemical Analysis |
title_full_unstemmed | Design and Construction of an Equibiaxial Cell Stretching System That Is Improved for Biochemical Analysis |
title_short | Design and Construction of an Equibiaxial Cell Stretching System That Is Improved for Biochemical Analysis |
title_sort | design and construction of an equibiaxial cell stretching system that is improved for biochemical analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3953117/ https://www.ncbi.nlm.nih.gov/pubmed/24626190 http://dx.doi.org/10.1371/journal.pone.0090665 |
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