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Take a microplate with transwell inserts coated with ECM proteins to promote cell adhesion.
Add Human brain microvascular endothelial cells, or HBMECs , into the inserts and a growth medium to the lower compartments.
Incubate, allowing the cells to adhere and grow into a monolayer. These cells express tight junctions, mimicking the blood-brain barrier endothelium that limits the passage of cells and molecules.
Remove the medium. Add peripheral blood mononuclear cells, or PBMCs, to the inserts and a culture medium to the lower compartments.
Incubate, allowing PBMC lymphocytes to interact with the endothelial cells and then pass between them, a process called transmigration.
Rinse the insert bottom, collecting the adhered transmigrated cells into the lower compartments.
Introduce fluorescent microbeads as a reference for cell quantification.
Transfer the suspension into a tube, centrifuge, discard the supernatant, and resuspend in a fluorophore-conjugated antibody cocktail to label the lymphocytes.
The transmigrated lymphocytes are ready for quantification via flow cytometry.
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