Volume 17, Issue 3 2005759
Full Paper

An Acoustic Platform for Single-Cell, High-Throughput Measurements of the Viscoelastic Properties of Cells

Valentin Romanov

Corresponding Author

Valentin Romanov

Department of Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute, Darlinghurst, Sydney, NSW, 2010 Australia

E-mail: [email protected]; [email protected]

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Giulia Silvani

Corresponding Author

Giulia Silvani

Department of Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute, Darlinghurst, Sydney, NSW, 2010 Australia

E-mail: [email protected]; [email protected]

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Huiyu Zhu

Huiyu Zhu

Faculty of Science, University of Technology Sydney, Ultimo, Sydney, NSW, 2007 Australia

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Charles D. Cox

Charles D. Cox

Department of Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute, Darlinghurst, Sydney, NSW, 2010 Australia

St Vincent's Clinical School, University of New South Wales, Sydney, NSW, 2010 Australia

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Boris Martinac

Boris Martinac

Department of Molecular Cardiology and Biophysics, Victor Chang Cardiac Research Institute, Darlinghurst, Sydney, NSW, 2010 Australia

St Vincent's Clinical School, University of New South Wales, Sydney, NSW, 2010 Australia

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First published: 16 December 2020
Citations: 17

Abstract

Cellular processes including adhesion, migration, and differentiation are governed by the distinct mechanical properties of each cell. Importantly, the mechanical properties of individual cells can vary depending on local physical and biochemical cues in a time-dependent manner resulting in significant inter-cell heterogeneity. While several different methods have been developed to interrogate the mechanical properties of single cells, throughput to capture this heterogeneity remains an issue. Here, single-cell, high-throughput characterization of adherent cells is demonstrated using acoustic force spectroscopy (AFS). AFS works by simultaneously, acoustically driving tens to hundreds of silica beads attached to cells away from the cell surface, allowing the user to measure the stiffness of adherent cells under multiple experimental conditions. It is shown that cells undergo marked changes in viscoelasticity as a function of temperature, by altering the temperature within the AFS microfluidic circuit between 21 and 37 °C. In addition, quantitative differences in cells exposed to different pharmacological treatments specifically targeting the membrane–cytoskeleton interface are shown. Further, the high-throughput format of the AFS is utilized to rapidly probe, in excess of 1000 cells, three different cell lines expressing different levels of a mechanosensitive protein, Piezo1, demonstrating the ability to differentiate between cells based on protein expression levels.

Conflict of Interest

The authors declare no conflict of interest.

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