Signaling role of intracellular iron in NF-kappaB activation

J Biol Chem. 2003 May 16;278(20):17646-54. doi: 10.1074/jbc.M210905200. Epub 2003 Mar 11.

Abstract

Iron chelators inhibit endotoxin-induced NF-kappaB activation in hepatic macrophages (HMs), suggesting a role for the intracellular chelatable pool of iron in NF-kappaB activation. The present study tested this hypothesis. Analysis of Fe(59)-loaded HMs stimulated with lipopolysaccharide (LPS), revealed a previously unreported, transient rise in intracellular low molecular weight (LMW).Fe(59) complex ([LMW.Fe](i)) at </=2 min returning to the basal level within 15 min. The [LMW.Fe](i) response preceded IkappaB kinase (IKK) (>/=15 min) and NF-kappaB (>/=30 min) activation. Iron chelators (1,2-dimethyl-3-hydroxypyridin-4-one and N,N'-bis-2-hydroxybenzylethylenediamine-N,N'-diacetic acid) abrogated the [LMW.Fe](i) response and IKK and NF-kappaB activation. The [LMW.Fe](i) response was also observed in tumor necrosis factor alpha (TNFalpha)-stimulated HMs and RAW264.7 cells treated with LPS and interferon-gamma but not in primary rat hepatocytes or myofibroblastic cells exposed to LPS or TNFalpha. Both [LMW.Fe](i) response and IKK activation in LPS-stimulated HMs were inhibited by diphenylene iodonium (nonspecific inhibitor for flavin-containing oxidases), l-N(6)-(1-iminoethyl)lysine (selective iNOS inhibitor), and adenoviral-mediated expression of a dominant negative mutant of Rac1 or Cu,Zn-superoxide dismutase, suggesting the role of (.)NO and O(2)() in mediating the iron signaling. In fact, this inhibition was recapitulated by a cell-permeable scavenger of ONOO(-), 5,10,15,20-tetrakis (4-sulfonatophenyl)porphyrinato iron (III) chloride. Conversely, ONOO(-) alone induced both [LMW.Fe](i) response and IKK activation. Finally, direct addition of ferrous iron to cultured HMs activated IKK and NF-kappaB. These results support a novel signaling role for [LMW.Fe](i) in IKK activation, which appears to be induced by ONOO(-) and selectively operative in macrophages.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cation Transport Proteins / metabolism
  • Cell Nucleus / metabolism
  • Cells, Cultured
  • Chelating Agents / pharmacology
  • Dose-Response Relationship, Drug
  • Fibroblasts / metabolism
  • Hepatocytes / metabolism
  • I-kappa B Kinase
  • Immunoblotting
  • Iodine / pharmacology
  • Iron / metabolism*
  • Iron / pharmacology
  • Lipopolysaccharides / metabolism
  • Macrophages / metabolism
  • Male
  • Mice
  • NF-kappa B / metabolism*
  • Onium Compounds / pharmacology
  • Oxidation-Reduction
  • Protein Serine-Threonine Kinases / metabolism
  • Rats
  • Rats, Wistar
  • Signal Transduction*
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cation Transport Proteins
  • Chelating Agents
  • Lipopolysaccharides
  • NF-kappa B
  • Onium Compounds
  • Tumor Necrosis Factor-alpha
  • natural resistance-associated macrophage protein 1
  • diphenyleneiodonium
  • Iodine
  • Iron
  • Protein Serine-Threonine Kinases
  • Chuk protein, mouse
  • I-kappa B Kinase
  • Ikbkb protein, mouse
  • Ikbke protein, mouse