Cell visco-elasticity measured with AFM and optical trapping at sub-micrometer deformations.

The measurement of the elastic properties of cells is widely used as an indicator for cellular changes during differentiation, upon drug treatment, or resulting from the interaction with the supporting matrix. Elasticity is routinely quantified by indenting the cell with a probe of an AFM while appl...

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Autores principales: Schanila Nawaz, Paula Sánchez, Kai Bodensiek, Sai Li, Mikael Simons, Iwan A T Schaap
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:11243d4d5e6445fe98f05adc71b2fff22021-11-18T07:04:56ZCell visco-elasticity measured with AFM and optical trapping at sub-micrometer deformations.1932-620310.1371/journal.pone.0045297https://doaj.org/article/11243d4d5e6445fe98f05adc71b2fff22012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23028915/?tool=EBIhttps://doaj.org/toc/1932-6203The measurement of the elastic properties of cells is widely used as an indicator for cellular changes during differentiation, upon drug treatment, or resulting from the interaction with the supporting matrix. Elasticity is routinely quantified by indenting the cell with a probe of an AFM while applying nano-Newton forces. Because the resulting deformations are in the micrometer range, the measurements will be affected by the finite thickness of the cell, viscous effects and even cell damage induced by the experiment itself. Here, we have analyzed the response of single 3T3 fibroblasts that were indented with a micrometer-sized bead attached to an AFM cantilever at forces from 30-600 pN, resulting in indentations ranging from 0.2 to 1.2 micrometer. To investigate the cellular response at lower forces up to 10 pN, we developed an optical trap to indent the cell in vertical direction, normal to the plane of the coverslip. Deformations of up to two hundred nanometers achieved at forces of up to 30 pN showed a reversible, thus truly elastic response that was independent on the rate of deformation. We found that at such small deformations, the elastic modulus of 100 Pa is largely determined by the presence of the actin cortex. At higher indentations, viscous effects led to an increase of the apparent elastic modulus. This viscous contribution that followed a weak power law, increased at larger cell indentations. Both AFM and optical trapping indentation experiments give consistent results for the cell elasticity. Optical trapping has the benefit of a lower force noise, which allows a more accurate determination of the absolute indentation. The combination of both techniques allows the investigation of single cells at small and large indentations and enables the separation of their viscous and elastic components.Schanila NawazPaula SánchezKai BodensiekSai LiMikael SimonsIwan A T SchaapPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 9, p e45297 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Schanila Nawaz
Paula Sánchez
Kai Bodensiek
Sai Li
Mikael Simons
Iwan A T Schaap
Cell visco-elasticity measured with AFM and optical trapping at sub-micrometer deformations.
description The measurement of the elastic properties of cells is widely used as an indicator for cellular changes during differentiation, upon drug treatment, or resulting from the interaction with the supporting matrix. Elasticity is routinely quantified by indenting the cell with a probe of an AFM while applying nano-Newton forces. Because the resulting deformations are in the micrometer range, the measurements will be affected by the finite thickness of the cell, viscous effects and even cell damage induced by the experiment itself. Here, we have analyzed the response of single 3T3 fibroblasts that were indented with a micrometer-sized bead attached to an AFM cantilever at forces from 30-600 pN, resulting in indentations ranging from 0.2 to 1.2 micrometer. To investigate the cellular response at lower forces up to 10 pN, we developed an optical trap to indent the cell in vertical direction, normal to the plane of the coverslip. Deformations of up to two hundred nanometers achieved at forces of up to 30 pN showed a reversible, thus truly elastic response that was independent on the rate of deformation. We found that at such small deformations, the elastic modulus of 100 Pa is largely determined by the presence of the actin cortex. At higher indentations, viscous effects led to an increase of the apparent elastic modulus. This viscous contribution that followed a weak power law, increased at larger cell indentations. Both AFM and optical trapping indentation experiments give consistent results for the cell elasticity. Optical trapping has the benefit of a lower force noise, which allows a more accurate determination of the absolute indentation. The combination of both techniques allows the investigation of single cells at small and large indentations and enables the separation of their viscous and elastic components.
format article
author Schanila Nawaz
Paula Sánchez
Kai Bodensiek
Sai Li
Mikael Simons
Iwan A T Schaap
author_facet Schanila Nawaz
Paula Sánchez
Kai Bodensiek
Sai Li
Mikael Simons
Iwan A T Schaap
author_sort Schanila Nawaz
title Cell visco-elasticity measured with AFM and optical trapping at sub-micrometer deformations.
title_short Cell visco-elasticity measured with AFM and optical trapping at sub-micrometer deformations.
title_full Cell visco-elasticity measured with AFM and optical trapping at sub-micrometer deformations.
title_fullStr Cell visco-elasticity measured with AFM and optical trapping at sub-micrometer deformations.
title_full_unstemmed Cell visco-elasticity measured with AFM and optical trapping at sub-micrometer deformations.
title_sort cell visco-elasticity measured with afm and optical trapping at sub-micrometer deformations.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/11243d4d5e6445fe98f05adc71b2fff2
work_keys_str_mv AT schanilanawaz cellviscoelasticitymeasuredwithafmandopticaltrappingatsubmicrometerdeformations
AT paulasanchez cellviscoelasticitymeasuredwithafmandopticaltrappingatsubmicrometerdeformations
AT kaibodensiek cellviscoelasticitymeasuredwithafmandopticaltrappingatsubmicrometerdeformations
AT saili cellviscoelasticitymeasuredwithafmandopticaltrappingatsubmicrometerdeformations
AT mikaelsimons cellviscoelasticitymeasuredwithafmandopticaltrappingatsubmicrometerdeformations
AT iwanatschaap cellviscoelasticitymeasuredwithafmandopticaltrappingatsubmicrometerdeformations
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