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Updated: Oct 1, 2025

Assay of Adhesion Under Shear Stress for the Study of T Lymphocyte-Adhesion Molecule Interactions
Published on: June 29, 2016
Fluid shear stress enhances T cell activation through Piezo1
Jacob M Hope1, Jenna A Dombroski1, Rebecca S Pereles1
1Department of Biomedical Engineering, Vanderbilt University, 5824 Stevenson Center, Nashville, TN, 37235, USA.
Fluid shear stress (FSS) mechanically enhances T cell activation by increasing key signaling proteins and cytokine expression. This process is calcium-dependent and mediated by the Piezo1 channel, suggesting a link to autoimmune diseases.
Area of Science:
- Immunology
- Biophysics
- Cell Biology
Background:
- T cell activation involves both biochemical and mechanical processes.
- Fluid shear stress (FSS) is a mechanical force present in the circulatory system.
Purpose of the Study:
- To investigate the mechanical enhancement of T cell activation using FSS.
- To explore the role of FSS in T cell signaling and function.
Main Methods:
- Jurkat and primary human T cells were treated with FSS using a cone-and-plate viscometer.
- T cell activation markers, signaling protein phosphorylation, and cytokine expression were analyzed.
- Calcium signaling pathways and the involvement of the Piezo1 channel were investigated.
Main Results:
- FSS treatment, combined with CD3/CD28 stimulation, increased the activation of ZAP70, NFAT, NF-κB, and AP-1.
- Enhanced expression of TNF-α, IL-2, and IFN-γ was observed following FSS treatment.
- FSS-induced T cell activation was calcium-dependent and mediated by the mechanosensitive ion channel Piezo1.
Conclusions:
- FSS represents a novel mechanical factor influencing T cell activation dynamics.
- The circulatory FSS may play a proinflammatory role in T cell function.
- Abnormal blood flow and associated FSS could be linked to autoimmune diseases.
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