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Dynamic monitoring of cell mechanical properties using profile microindentation

We have developed a simple and relatively inexpensive system to visualize adherent cells in profile while measuring their mechanical properties using microindentation. The setup allows simultaneous control of cell microenvironment by introducing a micropipette for the delivery of soluble factors or...

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Detalles Bibliográficos
Autores principales: Guillou, L., Babataheri, A., Puech, P.-H., Barakat, A. I., Husson, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746699/
https://www.ncbi.nlm.nih.gov/pubmed/26857265
http://dx.doi.org/10.1038/srep21529
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author Guillou, L.
Babataheri, A.
Puech, P.-H.
Barakat, A. I.
Husson, J.
author_facet Guillou, L.
Babataheri, A.
Puech, P.-H.
Barakat, A. I.
Husson, J.
author_sort Guillou, L.
collection PubMed
description We have developed a simple and relatively inexpensive system to visualize adherent cells in profile while measuring their mechanical properties using microindentation. The setup allows simultaneous control of cell microenvironment by introducing a micropipette for the delivery of soluble factors or other cell types. We validate this technique against atomic force microscopy measurements and, as a proof of concept, measure the viscoelastic properties of vascular endothelial cells in terms of an apparent stiffness and a dimensionless parameter that describes stress relaxation. Furthermore, we use this technique to monitor the time evolution of these mechanical properties as the cells’ actin is depolymerized using cytochalasin-D.
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spelling pubmed-47466992016-02-17 Dynamic monitoring of cell mechanical properties using profile microindentation Guillou, L. Babataheri, A. Puech, P.-H. Barakat, A. I. Husson, J. Sci Rep Article We have developed a simple and relatively inexpensive system to visualize adherent cells in profile while measuring their mechanical properties using microindentation. The setup allows simultaneous control of cell microenvironment by introducing a micropipette for the delivery of soluble factors or other cell types. We validate this technique against atomic force microscopy measurements and, as a proof of concept, measure the viscoelastic properties of vascular endothelial cells in terms of an apparent stiffness and a dimensionless parameter that describes stress relaxation. Furthermore, we use this technique to monitor the time evolution of these mechanical properties as the cells’ actin is depolymerized using cytochalasin-D. Nature Publishing Group 2016-02-09 /pmc/articles/PMC4746699/ /pubmed/26857265 http://dx.doi.org/10.1038/srep21529 Text en Copyright © 2016, Macmillan Publishers Limited 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
Guillou, L.
Babataheri, A.
Puech, P.-H.
Barakat, A. I.
Husson, J.
Dynamic monitoring of cell mechanical properties using profile microindentation
title Dynamic monitoring of cell mechanical properties using profile microindentation
title_full Dynamic monitoring of cell mechanical properties using profile microindentation
title_fullStr Dynamic monitoring of cell mechanical properties using profile microindentation
title_full_unstemmed Dynamic monitoring of cell mechanical properties using profile microindentation
title_short Dynamic monitoring of cell mechanical properties using profile microindentation
title_sort dynamic monitoring of cell mechanical properties using profile microindentation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4746699/
https://www.ncbi.nlm.nih.gov/pubmed/26857265
http://dx.doi.org/10.1038/srep21529
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