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Published online before print May 22, 2003
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Article |
-inducible genes by iron in human monocytic cells
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*Department of Internal Medicine, University Hospital Innsbruck, Austria; and
Institute for Medical Chemistry and Biochemistry, University of Innsbruck, Austria
@ To whom correspondence should be addressed. E-mail: guenter.weiss{at}uibk.ac.at.
| Abstract |
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To elucidate iron-regulated interferon-
(IFN-
) effector functions, we investigated three IFN-
-inducible genes [intercellular adhesion molecule-1 (ICAM-1), human leukocyte antigen (HLA)-DR, guanosine 5`-triphosphate-cyclohydrolase I (GTP-CH)] in primary human monocytes and the cell line THP-1. IFN-
increased the surface expression of ICAM-1 and HLA-DR and stimulated GTP-CH activity. Addition of iron before cytokine stimulation resulted in a dose-dependent reduction of these pathways, and iron restriction by desferrioxamine (DFO) enhanced ICAM-1, HLA-DR, and GTP-CH expression. Iron neither affected IFN-
binding to its receptor nor IFN-
receptor surface expression. IFN-
-inducible mRNA expression of ICAM-1, HLA-DR, and GTP-CH was reduced by iron and increased by DFO by a transcriptional mechanism. Moreover, ICAM-1 and to a lesser extent, GTP-CH and HLA-DR mRNA expression were regulated post-transcriptionally, as iron pretreatment resulted in shortening the mRNA half-life compared with cells treated with IFN-
alone. Thus, iron perturbations regulate IFN-
effector pathways by transcriptional and post-transcriptional mechanisms, indicating that iron rather interferes with IFN-
signal-transduction processes.
Key Words: monocytes/macrophages gene regulation cytokines adhesion molecules
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