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Updated: May 16, 2026

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Laminar Flow-based Assays to Investigate Leukocyte Recruitment on Cultured Vascular Cells and Adherent Platelets
Published on: April 9, 2018
Studying leukocyte recruitment under flow conditions
Sean A Parsons1, Christophe Jurzinsky, Susan L Cuvelier
1Calvin, Phoebe and Joan Snyder Institute for Infection, Immunity and Inflammation, University of Calgary, Calgary, AB, Canada.
Methods in Molecular Biology (Clifton, N.J.)
|November 27, 2012
Summary
This study details methods for analyzing leukocyte recruitment using a parallel plate flow chamber. These techniques quantify leukocyte adhesion and transmigration under shear stress, crucial for understanding inflammatory responses.
Area of Science:
- Biomedical Engineering
- Cell Biology
- Immunology
Background:
- Leukocyte recruitment from blood vessels is a critical inflammatory process.
- This recruitment is influenced by haemodynamic shear stress.
- In vitro models are essential for studying these complex cellular interactions.
Purpose of the Study:
- To describe standardized methods for studying leukocyte recruitment under shear stress.
- To enable quantitative analysis of leukocyte adhesion and transmigration.
- To provide a versatile platform for investigating cell-cell interactions.
Main Methods:
- Utilizing a parallel plate flow chamber for in vitro studies.
- Employing whole blood or isolated leukocyte suspensions.
- Assessing interactions with endothelial cells under controlled shear conditions.
Main Results:
- Methods allow measurement of total recruited leukocytes, rolling/adherent percentages, and transmigration.
- The system is adaptable for various adhesive substrates and particles.
- Successful application to cytokine-stimulated and genetically modified endothelial cells.
Conclusions:
- The described flow chamber methods offer a robust and adaptable approach for studying leukocyte recruitment.
- These techniques are valuable for understanding inflammatory processes and cell adhesion.
- The methodology can be applied to diverse cell-substrate and cell-particle interaction studies.

