4.5 Article

Unbiased High-Precision Cell Mechanical Measurements with Microconstrictions

Journal

BIOPHYSICAL JOURNAL
Volume 112, Issue 7, Pages 1472-1480

Publisher

CELL PRESS
DOI: 10.1016/j.bpj.2017.02.018

Keywords

-

Categories

Funding

  1. German Science Foundation (DFG)
  2. Research Training Group 1962 Dynamic Interactions at Biological Membranes: From Single Molecules to Tissue''
  3. Emerging Fields Initiative of the University of Erlangen-Nuremberg

Ask authors/readers for more resources

We describe a quantitative, high-precision, high-throughput method for measuring the mechanical properties of cells in suspension with a microfluidic device, and for relating cell mechanical responses to protein expression levels. Using a high-speed (750 fps) charge-coupled device camera, we measure the driving pressure Delta p, maximum cell deformation epsilon(max), and entry time t(entry) of cells in an array of microconstrictions. From these measurements, we estimate population averages of elastic modulus E and fluidity beta (the power-law exponent of the cell deformation in response to a step change in pressure). We find that cell elasticity increases with increasing strain epsilon(max) according to E similar to epsilon(max), and with increasing pressure according to E similar to Delta p. Variable cell stress due to driving pressure fluctuations and variable cell strain due to cell size fluctuations therefore cause significant variability between measurements. To reduce measurement variability, we use a histogram matching method that selects and analyzes only those cells from different measurements that have experienced the same pressure and strain. With this method, we investigate the influence of measurement parameters on the resulting cell elastic modulus and fluidity. We find a small but significant softening of cells with increasing time after cell harvesting. Cells harvested from confluent cultures are softer compared to cells harvested from subconfluent cultures. Moreover, cell elastic modulus increases with decreasing concentration of the adhesion-reducing surfactant pluronic. Lastly, we simultaneously measure cell mechanics and fluorescence signals of cells that overexpress the GFP-tagged nuclear envelope protein lamin A. We find a dose-dependent increase in cell elastic modulus and decrease in cell fluidity with increasing lamin A levels. Together, our findings demonstrate that histogram matching of pressure, strain, and protein expression levels greatly reduces the variability between measurements and enables us to reproducibly detect small differences in cell mechanics.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available