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

被引:86
|
作者
Fregin, Bob [1 ]
Czerwinski, Fabian [1 ]
Biedenweg, Doreen [2 ]
Girardo, Salvatore [3 ]
Gross, Stefan [2 ,4 ]
Aurich, Konstanze [2 ]
Otto, Oliver [1 ,4 ]
机构
[1] Ernst Moritz Arndt Univ Greifswald, Zentrum Innovat Kompetenz Humorale Immunreakt Kar, Fleischmannstr 42, D-17489 Greifswald, Germany
[2] Univ Med Greifswald, Fleischmannstr 8, D-17489 Greifswald, Germany
[3] Tech Univ Dresden, Ctr Biotechnol, Ctr Mol & Cellular Bioengn, Tatzberg 47-49, D-01307 Dresden, Germany
[4] Univ Med Greifswald, Standort Greifswald, Deutsch Zentrum Herz Kreislauf Forsch eV, Fleischmannstr 42, D-17489 Greifswald, Germany
关键词
STEM-CELLS; MECHANICS; NEUTROPHILS; TOOL;
D O I
10.1038/s41467-019-08370-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:11
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