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RECEPTORS AND SIGNAL TRANSDUCTION
B activation, I
B-
degradation, and proteasome activity in neutrophils1Department of Medicine, 2Center for Free Radical Biology, University of Alabama, Birmingham, Alabama
Submitted 12 December 2006 ; accepted in final form 22 March 2007
Although ROS can participate in modulating the activity of the transcriptional factor NF-
B and expression of NF-
B-dependent genes, the mechanisms involved and the roles of specific ROS have not been fully determined. In particular, individual ROS appear to have differing effects on NF-
B activation dependent on the cell population studied. In the present study, we examined the ability of H2O2 to affect NF-
B activation in LPS-stimulated murine neutrophils and macrophages. Exposure of bone marrow or peritoneal neutrophils to H2O2 was associated with reduced nuclear translocation of NF-
B and decreased production of the NF-
B-dependent cytokines TNF-
and macrophage inhibitory protein-2. H2O2 treatment resulted in diminished trypsin- and chymotrypsin-like proteasome activity. The degradation of I
B-
normally found in LPS-treated neutrophils was prevented when H2O2 was added to cell cultures. In contrast to the effects found in neutrophils, H2O2 did not affect chymotrypsin-like proteasomal activity or cytokine production in LPS-stimulated macrophages, even though trypsin-like proteasomal activity was reduced. These results demonstrate that the effects of H2O2 on NF-
B and proteasomal activity are cell population specific.
reactive oxygen species; signal transduction; nuclear factor-
B
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