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A single‐step, sensitive flow cytofluorometric assay for the simultaneous assessment of membrane‐bound and ingested Candida albicans in phagocytosing neutrophils
Author(s) -
Busetto Sara,
Trevisan Elisa,
Patriarca Pierluigi,
Menegazzi Renzo
Publication year - 2004
Publication title -
cytometry part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 90
eISSN - 1552-4930
pISSN - 1552-4922
DOI - 10.1002/cyto.a.20014
Subject(s) - flow cytometry , candida albicans , propidium iodide , trypan blue , phagocytosis , fluorescence , population , yeast , fluorescein , biology , microbiology and biotechnology , biophysics , reproducibility , cytometry , chromatography , chemistry , cell , biochemistry , medicine , programmed cell death , apoptosis , physics , environmental health , quantum mechanics
Background Distinguishing ingested particles from those attached to the cell surface is an essential requirement when performing quantitative studies of phagocytosis. In the present report, we describe a simple, sensitive and reliable flow cytofluorometric method that achieves this goal in a Candida albicans ‐human neutrophils (PMN) system. Methods The assay is based on the observation that the vital dye trypan blue (TB), while quenching the green fluorescence of fluorescein‐labeled C. albicans , causes them to fluoresce red. PMN were incubated with fluorescein‐labeled yeast particles for the required time. Aliquots of the incubation mixtures were then promptly diluted with an equal volume of a TB solution at pH 4.0, and subsequently analyzed by flow cytometry for green and red fluorescence. Results Since TB does not penetrate into the cells, ingested yeasts retain their green fluorescence, while membrane‐bound particles display a red fluorescence. Conclusions Our fluorescence flow cytometric method enables to simultaneously distinguish, within the leukocyte population, cell subsets with attached and ingested yeast particles. Its major features are: (1) accuracy, sensitivity and reproducibility; (2) no further sample manipulations after completion of phagocytosis; (3) possibility of counting free, attached and internalized yeast particles; and (4) use of a nontoxic reagent (TB). © 2004 Wiley‐Liss, Inc.