Single-Cell Elasticity Measurement with an Optically Actuated Microrobot

A cell elasticity measurement method is introduced that uses polymer microtools actuated by holographic optical tweezers. The microtools were prepared with two-photon polymerization. Their shape enables the approach of the cells in any lateral direction. In the presented case, endothelial cells grow...

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Main Authors: István Grexa, Tamás Fekete, Judit Molnár, Kinga Molnár, Gaszton Vizsnyiczai, Pál Ormos, Lóránd Kelemen
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Micromachines
Subjects:
Online Access:https://www.mdpi.com/2072-666X/11/9/882
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spelling doaj-b3a6b577bef84c59813fc7d79940af1b2020-11-25T03:41:59ZengMDPI AGMicromachines2072-666X2020-09-011188288210.3390/mi11090882Single-Cell Elasticity Measurement with an Optically Actuated MicrorobotIstván Grexa0Tamás Fekete1Judit Molnár2Kinga Molnár3Gaszton Vizsnyiczai4Pál Ormos5Lóránd Kelemen6Biological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryBiological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryBiological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryBiological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryBiological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryBiological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryBiological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryA cell elasticity measurement method is introduced that uses polymer microtools actuated by holographic optical tweezers. The microtools were prepared with two-photon polymerization. Their shape enables the approach of the cells in any lateral direction. In the presented case, endothelial cells grown on vertical polymer walls were probed by the tools in a lateral direction. The use of specially shaped microtools prevents the target cells from photodamage that may arise during optical trapping. The position of the tools was recorded simply with video microscopy and analyzed with image processing methods. We critically compare the resulting Young’s modulus values to those in the literature obtained by other methods. The application of optical tweezers extends the force range available for cell indentations measurements down to the fN regime. Our approach demonstrates a feasible alternative to the usual vertical indentation experiments.https://www.mdpi.com/2072-666X/11/9/882cell elasticityendothelial cellsoptical micromanipulationholographic optical tweezerstwo-photon polymerizationimage processing
collection DOAJ
language English
format Article
sources DOAJ
author István Grexa
Tamás Fekete
Judit Molnár
Kinga Molnár
Gaszton Vizsnyiczai
Pál Ormos
Lóránd Kelemen
spellingShingle István Grexa
Tamás Fekete
Judit Molnár
Kinga Molnár
Gaszton Vizsnyiczai
Pál Ormos
Lóránd Kelemen
Single-Cell Elasticity Measurement with an Optically Actuated Microrobot
Micromachines
cell elasticity
endothelial cells
optical micromanipulation
holographic optical tweezers
two-photon polymerization
image processing
author_facet István Grexa
Tamás Fekete
Judit Molnár
Kinga Molnár
Gaszton Vizsnyiczai
Pál Ormos
Lóránd Kelemen
author_sort István Grexa
title Single-Cell Elasticity Measurement with an Optically Actuated Microrobot
title_short Single-Cell Elasticity Measurement with an Optically Actuated Microrobot
title_full Single-Cell Elasticity Measurement with an Optically Actuated Microrobot
title_fullStr Single-Cell Elasticity Measurement with an Optically Actuated Microrobot
title_full_unstemmed Single-Cell Elasticity Measurement with an Optically Actuated Microrobot
title_sort single-cell elasticity measurement with an optically actuated microrobot
publisher MDPI AG
series Micromachines
issn 2072-666X
publishDate 2020-09-01
description A cell elasticity measurement method is introduced that uses polymer microtools actuated by holographic optical tweezers. The microtools were prepared with two-photon polymerization. Their shape enables the approach of the cells in any lateral direction. In the presented case, endothelial cells grown on vertical polymer walls were probed by the tools in a lateral direction. The use of specially shaped microtools prevents the target cells from photodamage that may arise during optical trapping. The position of the tools was recorded simply with video microscopy and analyzed with image processing methods. We critically compare the resulting Young’s modulus values to those in the literature obtained by other methods. The application of optical tweezers extends the force range available for cell indentations measurements down to the fN regime. Our approach demonstrates a feasible alternative to the usual vertical indentation experiments.
topic cell elasticity
endothelial cells
optical micromanipulation
holographic optical tweezers
two-photon polymerization
image processing
url https://www.mdpi.com/2072-666X/11/9/882
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