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A one-step procedure to probe the viscoelastic properties of cells by Atomic Force Microscopy

The increasingly recognised importance of viscoelastic properties of cells in pathological conditions requires rapid development of advanced cell microrheology technologies. Here, we present a novel Atomic Force Microscopy (AFM)-microrheology (AFM(2)) method for measuring the viscoelastic properties...

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Autores principales: Chim, Ya Hua, Mason, Louise M., Rath, Nicola, Olson, Michael F., Tassieri, Manlio, Yin, Huabing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160452/
https://www.ncbi.nlm.nih.gov/pubmed/30262873
http://dx.doi.org/10.1038/s41598-018-32704-8
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author Chim, Ya Hua
Mason, Louise M.
Rath, Nicola
Olson, Michael F.
Tassieri, Manlio
Yin, Huabing
author_facet Chim, Ya Hua
Mason, Louise M.
Rath, Nicola
Olson, Michael F.
Tassieri, Manlio
Yin, Huabing
author_sort Chim, Ya Hua
collection PubMed
description The increasingly recognised importance of viscoelastic properties of cells in pathological conditions requires rapid development of advanced cell microrheology technologies. Here, we present a novel Atomic Force Microscopy (AFM)-microrheology (AFM(2)) method for measuring the viscoelastic properties in living cells, over a wide range of continuous frequencies (0.005 Hz ~ 200 Hz), from a simple stress-relaxation nanoindentation. Experimental data were directly analysed without the need for pre-conceived viscoelastic models. We show the method had an excellent agreement with conventional oscillatory bulk-rheology measurements in gels, opening a new avenue for viscoelastic characterisation of soft matter using minute quantity of materials (or cells). Using this capability, we investigate the viscoelastic responses of cells in association with cancer cell invasive activity modulated by two important molecular regulators (i.e. mutation of the p53 gene and Rho kinase activity). The analysis of elastic (G′(ω)) and viscous (G″(ω)) moduli of living cells has led to the discovery of a characteristic transitions of the loss tangent (G″(ω)/G′(ω)) in the low frequency range (0.005 Hz ~ 0.1 Hz) that is indicative of the capability for cell restructuring of F-actin network. Our method is ready to be implemented in conventional AFMs, providing a simple yet powerful tool for measuring the viscoelastic properties of living cells.
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spelling pubmed-61604522018-09-28 A one-step procedure to probe the viscoelastic properties of cells by Atomic Force Microscopy Chim, Ya Hua Mason, Louise M. Rath, Nicola Olson, Michael F. Tassieri, Manlio Yin, Huabing Sci Rep Article The increasingly recognised importance of viscoelastic properties of cells in pathological conditions requires rapid development of advanced cell microrheology technologies. Here, we present a novel Atomic Force Microscopy (AFM)-microrheology (AFM(2)) method for measuring the viscoelastic properties in living cells, over a wide range of continuous frequencies (0.005 Hz ~ 200 Hz), from a simple stress-relaxation nanoindentation. Experimental data were directly analysed without the need for pre-conceived viscoelastic models. We show the method had an excellent agreement with conventional oscillatory bulk-rheology measurements in gels, opening a new avenue for viscoelastic characterisation of soft matter using minute quantity of materials (or cells). Using this capability, we investigate the viscoelastic responses of cells in association with cancer cell invasive activity modulated by two important molecular regulators (i.e. mutation of the p53 gene and Rho kinase activity). The analysis of elastic (G′(ω)) and viscous (G″(ω)) moduli of living cells has led to the discovery of a characteristic transitions of the loss tangent (G″(ω)/G′(ω)) in the low frequency range (0.005 Hz ~ 0.1 Hz) that is indicative of the capability for cell restructuring of F-actin network. Our method is ready to be implemented in conventional AFMs, providing a simple yet powerful tool for measuring the viscoelastic properties of living cells. Nature Publishing Group UK 2018-09-27 /pmc/articles/PMC6160452/ /pubmed/30262873 http://dx.doi.org/10.1038/s41598-018-32704-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chim, Ya Hua
Mason, Louise M.
Rath, Nicola
Olson, Michael F.
Tassieri, Manlio
Yin, Huabing
A one-step procedure to probe the viscoelastic properties of cells by Atomic Force Microscopy
title A one-step procedure to probe the viscoelastic properties of cells by Atomic Force Microscopy
title_full A one-step procedure to probe the viscoelastic properties of cells by Atomic Force Microscopy
title_fullStr A one-step procedure to probe the viscoelastic properties of cells by Atomic Force Microscopy
title_full_unstemmed A one-step procedure to probe the viscoelastic properties of cells by Atomic Force Microscopy
title_short A one-step procedure to probe the viscoelastic properties of cells by Atomic Force Microscopy
title_sort one-step procedure to probe the viscoelastic properties of cells by atomic force microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160452/
https://www.ncbi.nlm.nih.gov/pubmed/30262873
http://dx.doi.org/10.1038/s41598-018-32704-8
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