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Interindividual variation of NET osis in healthy donors: introduction and application of a refined method for extracellular trap quantification
Author(s) -
Hoffmann Jochen H. O.,
Schaekel Knut,
Gaiser Maria R.,
Enk Alexander H.,
Hadaschik Eva N.
Publication year - 2016
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/exd.13125
Subject(s) - neutrophil extracellular traps , coefficient of variation , extracellular , immunology , stimulation , flow cytometry , chemistry , microbiology and biotechnology , medicine , biology , biochemistry , inflammation , chromatography
Neutrophil extracellular trap ( NET ) formation is a mechanism of innate immune defence by which neutrophil (polymorphonuclear) granulocytes ( PMN ) produce net‐like structures of decondensed chromatin decorated with antimicrobial peptides for trapping and possibly killing microorganisms. If this process leads to cell death, it is termed NET osis. Alterations of this particular mechanism have been reported to be involved in the pathogenesis of chronic inflammatory diseases including psoriasis and lupus erythematosus. Still, quantification of NET osis poses a considerable challenge. We report and test a refined protocol for morphological NET quantification in healthy human donors that encompasses isolation, stimulation, DNA staining, live imaging and semi‐automated offline analysis. The results were highly reproducible and in good agreement with manual counting. The average intra‐donor coefficient of variation of NET osis rates to phorbol myristate acetate ( PMA ) stimulation was low compared to the respective interdonor coefficient of variation (10% vs 82%, n=4, respectively, if experiments were repeated on the same day, and 38% vs 74%, n=6, respectively, if experiments were repeated on average 42±34 days apart). Overall, the interdonor coefficient of variation was 67% (n=10). These findings altogether support the existence of a distinct predisposition of PMN from different donors for undergoing NET osis. Picogreen fluorescence correlated stronger to cell death than to morphological NET osis ( r 2 =.89, P <.001, n=8, and r 2 =.68, P =.012, n=8, respectively). This indicates that cytotoxicity may confound Picogreen fluorescence. Our results and the related protocol may help investigators with the quantification of NET osis and the design of respective basic and translational research studies.