| Literature DB >> 30450827 |
Susann Hartung1,2,3, Christopher Rauh1, Thi Ngoc Mai Hoang3,4, Susanne Jahreis1,3, Kathleen Wagner1,2,3, Juliane Macheleidt3, Axel A Brakhage3,4, Silke Rummler5, Andreas Hochhaus1, Marie von Lilienfeld-Toal1,2,3.
Abstract
Systemic infections with the opportunistic mold Aspergillus fumigatus are a great threat to immunocompromised patients such as transplant recipients. Immunological research on A. fumigatus involves the measurement of phagocytosis of fungal conidia (spores) by human phagocytes. Here, we present a fast and flexible way to analyze phagocytosis by flow cytometry using fluorescein isothiocyanate (FITC) labeling of conidia prior to co-incubation with human leukocytes and an anti-FITC counterstaining step postincubation to allow the discrimination of internalized and adherent conidia. In contrast to many other protocols, this method can be combined with further surface marker analyses. We sought to determine phagocytosis rates of A. fumigatus conidia in different stages and after several incubation times using this method. Moreover, we provide an example of application by comparing phagocytosis of A. fumigatus mutants to the wild type.Entities:
Keywords: zzm321990Aspergillus fumigatus; FITC; anti-FITC antibody; flow cytometry; phagocytosis
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Year: 2018 PMID: 30450827 DOI: 10.1002/cyto.a.23653
Source DB: PubMed Journal: Cytometry A ISSN: 1552-4922 Impact factor: 4.355