Am. J. Respir. Cell Mol. Biol., Vol 11, No. 5, 11 1994, 625-630.
Nitric oxide inactivates xanthine dehydrogenase and xanthine oxidase in interferon-gamma-stimulated macrophages
JE Rinaldo, M Clark, J Parinello and VL Shepherd
Department of Veterans' Affairs, Nashville, Tennessee.
Interferon-gamma (IFN-gamma) has been reported to up-regulate transcription
of the xanthine dehydrogenase (XDH) gene and to regulate XDH and xanthine
oxidase (XO) activity in endothelial cells and liver tissue. Macrophages
are a source of XDH/XO activity at inflammatory sites and are functionally
regulated by IFN-gamma. We studied the effect of IFN-gamma on XDH and XO in
rat bone marrow macrophages, rat alveolar macrophages, and murine RAW
cells. Instead of an induction of enzyme activity, XDH/XO activity was
almost totally lost after incubation with 100 to 1,000 U/ml of IFN-gamma
for 24 h in all three cell types. The loss of cell-associated XDH/XO
activity was not correlated with the appearance of XDH/XO activity in the
media. In addition, the loss of XDH/XO activity could not be accounted for
by transcriptional repression, since there was an increase in steady-state
levels of XDH mRNA. To determine whether XDH/XO activity might be lost
through nitric oxide-mediated inactivation of XDH/XO, we compared the time
course and dose response for XDH/XO inactivation with that of nitric oxide
production and found them similar. Treatment with the nitric oxide
inhibitor N-monomethyl arginine appeared to totally block inactivation of
XDH/XO by IFN-gamma. We conclude that upon stimulation with IFN-gamma,
inducible nitric oxide in macrophages leads to post- transcriptional
inhibition of XDH/XO, possibly minimizing the potential for tissue injury
from XO released from macrophages into the inflammatory milieu.
Inactivation of XDH may represent yet another "protective" role for nitric
oxide at sites of inflammation.
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Copyright © 1994 American Thoracic Society.
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