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J. Biol. Chem., Vol. 269, Issue 52, 32979-32984, Dec, 1994
SL Hempel, MM Monick, B He, T Yano and GW Hunninghake
We previously demonstrated that lipopolysaccharide (LPS) increases
expression of the prostaglandin H synthase-2 (PGHS-2) gene (Hempel, S.L.,
Monick, M.M., and Hunninghake, G.W. (1994) J. Clin. Invest. 93, 391-396).
In this study, the expression of the PGHS-2 gene in response to changes in
cell oxidant tone was studied. During LPS exposure, inhibition of synthesis
of the free radical, NO., resulted in a small decrease in prostaglandin E2
synthesis that did not reach statistical significance. There was no effect
on enzyme mass or mRNA. In contrast, incubation of alveolar macrophages in
the presence of LPS plus the antioxidant pyrrolidine dithiocarbamate, the
spin trap 5,5-dimethyl-1- pyrroline-N-oxide, or hypoxia, resulted in near
complete inhibition of prostaglandin E2 synthesis, PGHS-2 enzyme synthesis,
and gene transcription of PGHS-2 mRNA. There was no evidence of
cytotoxicity. These results demonstrate that synthesis of PGHS-2 in
response to LPS is inhibited by agents that decrease cell oxidant tone.
Synthesis of prostaglandin H synthase-2 by human alveolar macrophages in response to lipopolysaccharide is inhibited by decreased cell oxidant tone
Department of Medicine, University of Iowa, Iowa City 52242.
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