Related Experiment Video
Updated: Feb 20, 2026

09:12
Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry
Published on: January 12, 2018
15.5K
Real-Time Deformability Cytometry: Label-Free Functional Characterization of Cells
Maik Herbig1, Martin Kräter2, Katarzyna Plak1
1Biotechnology Center, Technische Universität Dresden, Tatzberg 47/49, 01307, Dresden, Germany.
Methods in Molecular Biology (Clifton, N.J.)
|October 27, 2017
Summary
Real-time deformability cytometry (RT-DC) offers high-throughput analysis of cell mechanics and morphology. This study provides essential guidelines for RT-DC data measurement and processing to standardize this powerful technique.
Area of Science:
- Biophysics
- Cell Biology
- Microfluidics
Background:
- Real-time deformability cytometry (RT-DC) is a microfluidic technique for high-throughput cell analysis.
- It measures cell morphology and rheology by deforming cells using hydrodynamic forces in a constricted channel.
- RT-DC captures up to 1000 cells/s without mechanical contact or staining, storing images for further analysis.
Purpose of the Study:
- To address the analytical challenges posed by the abundance of parameters in RT-DC data.
- To provide standardized guidelines for measuring and post-processing RT-DC data.
- To facilitate the interpretation of mechanical readouts from RT-DC.
Main Methods:
- Utilizing microfluidic channels for hydrodynamic cell deformation.
- Real-time quantification of cell morphology and rheology.
- Image segmentation for detailed cellular analysis.
Main Results:
- RT-DC is sensitive to cytoskeletal alterations, enabling differentiation of cell cycle phases.
- The technique can identify distinct subpopulations within whole blood samples.
- RT-DC can detect mechanical stiffening in cells entering a dormant state.
Conclusions:
- Standardized guidelines are crucial for the accurate interpretation of RT-DC data.
- RT-DC is a versatile tool for studying cell mechanics and heterogeneity.
- This work aims to enhance the analytical reproducibility and application scope of RT-DC.
Related Concept Videos
Flow Cytometry
16.6K
The development of flow cytometry techniques began in 1934 with initial attempts by Andrew Moldavan, a bacteriologist who counted the cells in a flowing capillary system. Moldavan pumped cells through a capillary tube focused under a microscope for visualization. The invention of photometry allowed the measurement of differentially-stained cells, and Louis Kamentsky developed the first multiparameter flow cytometer in 1965 to identify and count the cancer cells in cervical tissue specimens.
In...
In...
16.6K
Protein Dynamics in Living Cells
2.8K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
2.8K

