Leukocyte Adhesion Cascade

Study all steps of the leukocyte adhesion cascade with one system

The leukocyte adhesion cascade consists of capture, rolling, slow rolling, arrest, strengthening/spreading, and transmigration. Typically, analyses of these steps require at least 3 separate systems and/or assays.

BioFlux shear flow systems enable the visualization and analysis of all of the steps of the leukocyte adhesion cascade under physiological/pathological shear flow using one system.

General BioFlux workflow for cell adhesion cascade assays

Adhesion general workflow3

Leukocyte adhesion cascade assays using BioFlux

Adhesion: Recombinant human vimentin binds to P-selectin and blocks neutrophil capture and rolling on platelets and endothelium

The top channel shows the inhibition of neutrophil adhesion by recombinant human vimentin. The bottom channel shows neutrophil adhesion under control conditions.

Rolling: The vimentin rod domain blocks P-selectin-P-selectin glycoprotein ligand 1 interactions to attenuate leukocyte adhesion to inflamed endothelium

Neutrophil rolling on endothelial cells under shear flow. Scale bar = 50 µm

Transmigration: Ezrin and Moesin Are Required for Efficient T Cell Adhesion and Homing to Lymphoid Organs

Tracking of the transmigration of CMTMR stained wild-type T cells (red) and CFSE stained ERM-deficient T cells (green) through TNF-α treated 3B-11 endothelial cells. 

Scientific Poster: Fast, Scalable, and Physiological Leukocyte Adhesion Assays

Key BioFlux Advantages For Cell Adhesion Cascade Studies

FAQs:
Immune Cell Adhesion Assays Using the BioFlux

The BioFlux System provides a microfluidic platform that replicates physiological shearshear stress, making it ideal for modeling immune cell adhesion endothelial monolayers or ECM proteins. It enables real-time observation of immune cell dynamics under controlled flow conditions.

The BioFlux supports culturing endothelial cells directly in microfluidic channels and perfuse leukocytes or other immune cells under defined shear stress. This setup supports quantitative analysis of leukocyte adhesion in response to inflammatory stimuli.

The BioFlux integrates with standard microscopy platforms (contrast or fluorescence), enabling high-resolution live-cell imaging of leukocyte behavior.

Yes, the BioFlux is widely used in immunology research to study leukocyte recruitment during inflammation. Its ability to simulate vascular flow and endothelial activation makes it ideal for investigating immune cell trafficking in response to cytokines or chemokines.

The BioFlux replicates shear flow conditions that are essential for accurate modeling of leukocyte behavior. Unlike static assays, it allows for controlled shear stress, real-time imaging, and reproducible quantification of cell adhesion under physiologically relevant conditions.

The BioFlux offers well plate formats with 3, 8, and 24 microfluidic channels, allowing researchers to test multiple experimental conditions. This makes it ideal for comparing cytokine treatments, surface coatings, or leukocyte subtypes under flow.

Common substrates include endothelial cell monolayers, ICAM-1, VCAM-1, and selectins. BioFlux microfluidic channels can be coated or seeded with endothelial cells to mimic vascular surfaces, enabling targeted studies of leukocyte adhesion mechanisms.

Yes, the BioFlux supports perfusion of primary leukocytes, whole blood, or isolated immune cell populations.

FAQs:
Immune Cell Adhesion Assays Using the BioFlux

What microfluidic platform supports in vitro modeling of immune cell adhesion under flow?
The BioFlux System provides a microfluidic platform designed to replicate physiological shear stress, making it relevant for modeling immune cell adhesion to endothelial monolayers or ECM proteins. It enables real-time observation of immune cell dynamics under controlled flow conditions.
How can I study leukocyte-endothelial interactions using microfluidics?
The BioFlux supports culturing endothelial cells directly in microfluidic channels and perfusing leukocytes or other immune cells under defined shear stress. This setup supports quantitative analysis of leukocyte adhesion in response to inflammatory stimuli.
What are the advantages of using BioFlux over static leukocyte adhesion assays?
The BioFlux is designed to replicate shear flow conditions important for accurate modeling of leukocyte behavior. Unlike static assays, it supports controlled shear stress, real-time imaging, and reproducible quantification of cell adhesion under physiologically relevant conditions.
How does BioFlux support multi-condition leukocyte adhesion experiments?
The BioFlux offers well plate formats with 3, 8, and 24 microfluidic channels, allowing researchers to test multiple experimental conditions. This makes it ideal for comparing cytokine treatments, surface coatings, or leukocyte subtypes under flow.
What substrates can be used in the BioFlux microfluidic channels for leukocyte adhesion studies?
Common substrates include endothelial cell monolayers, ICAM-1, VCAM-1, and selectins. BioFlux microfluidic channels can be coated or seeded with endothelial cells to mimic vascular surfaces, enabling targeted studies of leukocyte adhesion mechanisms.
Is the BioFlux compatible with primary leukocytes or whole blood?
Yes. The BioFlux supports perfusion of primary leukocytes, whole blood, or isolated immune cell populations through microfluidic channels under controlled flow.

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