Literature DB >> 26153699

Microconstriction arrays for high-throughput quantitative measurements of cell mechanical properties.

Janina R Lange1, Julian Steinwachs1, Thorsten Kolb2, Lena A Lautscham1, Irina Harder3, Graeme Whyte4, Ben Fabry5.   

Abstract

We describe a method for quantifying the mechanical properties of cells in suspension with a microfluidic device consisting of a parallel array of micron-sized constrictions. Using a high-speed charge-coupled device camera, we measure the flow speed, cell deformation, and entry time into the constrictions of several hundred cells per minute during their passage through the device. From the flow speed and the occupation state of the microconstriction array with cells, the driving pressure across each constriction is continuously computed. Cell entry times into microconstrictions decrease with increased driving pressure and decreased cell size according to a power law. From this power-law relationship, the cell elasticity and fluidity can be estimated. When cells are treated with drugs that depolymerize or stabilize the cytoskeleton or the nucleus, elasticity and fluidity data from all treatments collapse onto a master curve. Power-law rheology and collapse onto a master curve are predicted by the theory of soft glassy materials and have been previously shown to describe the mechanical behavior of cells adhering to a substrate. Our finding that this theory also applies to cells in suspension provides the foundation for a quantitative high-throughput measurement of cell mechanical properties with microfluidic devices.
Copyright © 2015 Biophysical Society. Published by Elsevier Inc. All rights reserved.

Mesh:

Year:  2015        PMID: 26153699      PMCID: PMC4571004          DOI: 10.1016/j.bpj.2015.05.029

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  52 in total

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  38 in total

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3.  Unbiased High-Precision Cell Mechanical Measurements with Microconstrictions.

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4.  Measuring Cell Viscoelastic Properties Using a Microfluidic Extensional Flow Device.

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7.  The promise of single-cell mechanophenotyping for clinical applications.

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10.  Migration in Confined 3D Environments Is Determined by a Combination of Adhesiveness, Nuclear Volume, Contractility, and Cell Stiffness.

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Journal:  Biophys J       Date:  2015-09-01       Impact factor: 4.033

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