High-throughput single-cell rheology in complex samples by dynamic real-time deformability cytometry

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Bob Fregin - (Author)
  • Fabian Czerwinski - (Author)
  • Doreen Biedenweg - (Author)
  • Salvatore Girardo - , Technology Platform BIOTEC, TUD Dresden University of Technology (Author)
  • Stefan Gross - (Author)
  • Konstanze Aurich - (Author)
  • Oliver Otto - (Author)

Abstract

In life sciences, the material properties of suspended cells have attained significance close to that of fluorescent markers but with the advantage of label-free and unbiased sample characterization. Until recently, cell rheological measurements were either limited by acquisition throughput, excessive post processing, or low-throughput real-time analysis. Real-time deformability cytometry expanded the application of mechanical cell assays to fast on-the-fly phenotyping of large sample sizes, but has been restricted to single material parameters as the Young’s modulus. Here, we introduce dynamic real-time deformability cytometry for comprehensive cell rheological measurements at up to 100 cells per second. Utilizing Fourier decomposition, our microfluidic method is able to disentangle cell response to complex hydrodynamic stress distributions and to determine viscoelastic parameters independent of cell shape. We demonstrate the application of our technology for peripheral blood cells in whole blood samples including the discrimination of B- and CD4+ T-lymphocytes by cell rheological properties.

Details

Original languageEnglish
Article number415
JournalNature communications
Volume10
Issue number1
Publication statusPublished - 1 Dec 2019
Peer-reviewedYes

External IDs

PubMed 30679420