This video demonstrates a method for quantifying the phagocytosis of FITC-labeled pathogenic fungal spores by human leukocytes. Phagocytosed spores are discerned from cell-adherent spores through counterstaining, followed by flow cytometric analysis.
Protocol
All procedures involving sample collection have been performed in accordance with the institute's IRB guidelines. 1. Phagocytosis Assay Incubate 2 x 106 leukocytes and 4 x 106 FITC-labeled conidia (multiplicity of infection = 2) in 1.5 mL of RPMI + 10% FCS in a 12-well cell culture plate. As controls, include cells only (no conidia) and cells + unlabeled conidia. Place in a humidified CO2 incubator at 37 °C and in…
Disclosures
The authors have nothing to disclose.
Materials
Adhesive foil
Brand
701367
Cell culture plate, 12-well
Greiner Bio-one
665180
Cytometer
BD Biosciences
LSR Fortessa II, lasers: 488 nm (blue), 405 nm (violet), 355 nm (UV) and 640 nm (red)