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Nitroblue tetrazolium reduction in monocytes and monocyte‐derived macrophages
Author(s) -
MÜLLER FREDRIK,
ROLLAG HALVOR,
FRØLAND STIG S.
Publication year - 1989
Publication title -
apmis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.909
H-Index - 88
eISSN - 1600-0463
pISSN - 0903-4641
DOI - 10.1111/j.1699-0463.1989.tb00821.x
Subject(s) - zymosan , stimulation , monocyte , nitroblue tetrazolium , macrophage , endocrinology , medicine , chemistry , microbiology and biotechnology , phorbol , phagocytosis , andrology , in vitro , immunology , biology , biochemistry , protein kinase c , signal transduction
The ability to mount an oxidative burst (OB) in response to medium, zymosan and phorbol myristate acetate (PMA) was assessed in human blood monocytes cultured for 1 day (MO) and monocyte‐derived macrophages cultured for 10 days (MDM). Further, the effect of recombinant interferons (IFNs) on OB generation was examined. The OB was measured as a reduction of nitroblue tetrazolium (NBT). Unstimulated and stimulated NBT reduction per cell nucleus and the ratio of stimulated/unstimulated NBT reduction was not significantly different in cells cultured for 1 and 10 days. In MO, IFN‐γ stimulated the OB when co‐stimulated with zymosan or PMA. IFN‐α reduced MO adherence. When the lower adherence was corrected for, IFN‐α enhanced NBT reduction. In MDM, a high concentration of IFN‐γ stimulated the OB without co‐stimulation, in lower concentrations the presence of a co‐stimulant was necessary for OB stimulation. IFN‐α/β enhanced the OB in response to PMA, suggesting that IFN‐α/β has a role in macrophage activation.