Interferon gamma (IFN-gamma) priming is considered to be critical for inter
leukin 12 (IL-12) production of murine macrophages and human monocytes by l
ipopolysaccharide (LPS) stimulation. In our present experiments, freshly pr
epared spleen cells (f-spleen cells) were confirmed not to produce detectab
le level of IL-12 by LPS stimulation, although they produced Significant am
ount of IL-12 by the stimulation with LPS plus IFN-gamma, However, the stim
ulation only with LPS induced IL-12 production of spleen cells preincubated
in the absence of IFN-gamma. Findings on IL-12 p40 mRNA accumulation were
consistent with their IL-12 production. Essentially the same results were o
btained using spleen cells from IFN-gamma deficient mice. In the presence o
f anti-IL-10, f-spleen cells produced IL-12 upon LPS stimulation, indicatin
g that the failure of f-spleen cells in IL-12 production is caused by IL-10
produced by themselves upon LPS stimulation. In addition, f-spleen cells p
roduced IL-12 upon CD40 ligand stimulation, and the production was hardly a
ffected by the presence of IFN-gamma or preincubation, These results indica
te that IFN-gamma priming is not critical for IL-12 production of spleen ce
lls stimulated with LPS or CD40 ligand, although IFN-gamma enhances the pro
duction, especially, in response to LPS stimulation. (C) 2000 Academic Pres
s.