Development of oxidase ‘priming’ in maturing HL60 cells: Correlation with protein expression and tyrosine phosphorylation

Abstract

The mechanisms involved in ‘primi’ of the oxidase response of neutrophils are unknown. Two major problems are encountered in using circulating neutrophils; firstly, prior exposure to circulating ‘priming’ cytokines cannot be controlled and secondly, non-intentional ‘priming’ during cell separation can occur. In this study, these problems were avoided by differentiating the promyeloid leukaemic cell line, HL60, towards granulocytes using dibutyrl cyclic AMP, to produce a `virgin cell' model system. We have demonstrated that the ability of substance P to both prime the oxidase response and induce tyrosine phosphorylation increased during differentiation. The major tyrosine-phosphorylated protein, with molecular weight of 74 kDa, was not recognised by anti-c-rafl antibodies. Furthermore, c-rafl expression rapidly declined during HL60 cell granulocytic differentiation. This data shows that although there was no simple relationship between c-raf quantity and priming, the data were consistent with tyrosine phosphorylation of a 74 kDa protein being important for oxidase ‘priming’.