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Updated: Jun 12, 2026

Mechano-Node-Pore Sensing: A Rapid, Label-Free Platform for Multi-Parameter Single-Cell Viscoelastic Measurements
Published on: December 2, 2022
The viscoelastic properties of microvilli are dependent upon the cell-surface molecule
Johanne L Python1, Kristal O Wilson, Jeremy H Snook
1Department of Biomedical Engineering, University of Virginia, Box 800759, Charlottesville, VA 22908, USA.
Abstract:
We studied at nanometer resolution the viscoelastic properties of microvilli and tethers pulled from myelogenous cells via P-selectin glycoprotein ligand 1 (PSGL-1) and found that in contrast to pure membrane tethers, the viscoelastic properties of microvillus deformations are dependent upon the cell-surface molecule through which load is applied. A laser trap and polymer bead coated with anti-PSGL-1 (KPL-1) were used to apply step loads to microvilli. The lengthening of the microvillus in response to the induced step loads was fitted with a viscoelastic model. The quasi-steady state force on the microvillus at any given length was approximately fourfold lower in cells treated with cytochalasin D or when pulled with concanavalin A-coated rather than KPL-1-coated beads. These data suggest that associations between PSGL-1 and the underlying actin cytoskeleton significantly affect the early stages of leukocyte deformation under flow.
Insights
Leukocyte microvilli exhibit unique viscoelastic properties, differing from membrane tethers. Cell-surface molecule interactions, particularly with P-selectin glycoprotein ligand 1 (PSGL-1), significantly influence cell deformation dynamics.
Area of Science:
- Biophysics
- Cell Biology
- Immunology
Background:
- Leukocyte deformation is crucial for immune cell function under flow.
- Microvilli and membrane tethers are key structures involved in cell mechanics.
- P-selectin glycoprotein ligand 1 (PSGL-1) mediates cell adhesion and plays a role in leukocyte interactions.
Purpose of the Study:
- To investigate the viscoelastic properties of microvilli and tethers from myelogenous cells.
- To determine how cell-surface molecule interactions affect microvillus deformation.
- To elucidate the role of PSGL-1 in leukocyte mechanical responses.
Main Methods:
- Utilized nanometer-resolution techniques with a laser trap and polymer beads.
- Applied step loads to microvilli using beads coated with anti-PSGL-1 (KPL-1) or concanavalin A.
- Analyzed microvillus lengthening using a viscoelastic model.
Main Results:
- Microvillus viscoelastic properties depend on the specific cell-surface molecule mediating the load.
- Compared to pure membrane tethers, microvillus deformation is influenced by the applied force molecule.
- Cytochalasin D treatment or using concanavalin A-coated beads reduced the quasi-steady state force on microvilli.
Conclusions:
- PSGL-1 engagement with the actin cytoskeleton significantly impacts early leukocyte deformation.
- These findings provide insights into the mechanical basis of leukocyte behavior under shear stress.
- Understanding these viscoelastic properties is vital for comprehending immune cell trafficking and function.
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