D. Miyamoto et al., ANALYSIS OF THE NADPH OXIDASE COMPONENTS DURING DIFFERENTIATION OF HL-60 CELLS TO EOSINOPHILIC LINEAGE, Biochimica et biophysica acta. Molecular cell research, 1224(1), 1994, pp. 11-16
HL-60 cells were induced to differentiate into eosinophil-like cells w
ith sodium butyrate after passage under mild alkaline condition. The d
ifferentiating cells gradually possessed the Luxol-fast-blue (LFB) sta
ining-positive granules and the capacity to produce superoxide. The in
crease in the amounts of cytochrome b-558 paralleled the superoxide an
ion generating activity. Immunoblot analysis demonstrated that p47-pho
x cytosolic oxidase protein appeared 1 day after differentiation, and
increased up to 7 days. On the other hand, p67-phox cytosolic oxidase
protein appeared in 3 days, and increased gradually up to 7 days. The
oxidase activity did not appear until p67-phox protein was expressed i
n the cytosol during eosinophilic differentiation, indicating that p67
-phox protein is likely to be a key protein of cytosolic factors also
in eosinophilic differentiating cells. The amounts of p47-phox and p67
-phox translocated to the plasma membrane in response to phorbol myris
tate acetate (PMA) increased with increasing amounts of cytochrome b-5
58 in the membrane. Our data demonstrate that the appearance of NADPH
oxidase activity during eosinophilic differentiation is dependent on t
he levels of p47-phox and p67-phox cytosolic proteins translocated to
the plasma membrane and the amount of cytochrome b-558 in the membrane
as observed with neutrophils and monocytes.