Biosynthesis of nitric oxide activates iron regulatory factor in macrophages

EMBO J. 1993 Sep;12(9):3643-9. doi: 10.1002/j.1460-2075.1993.tb06038.x.

Abstract

Biosynthesis of nitric oxide (NO) from L-arginine modulates activity of iron-dependent enzymes, including mitochondrial acontiase, an [Fe-S] protein. We examined the effect of NO on the activity of iron regulatory factor (IRF), a cytoplasmic protein which modulates both ferritin mRNA translation and transferrin receptor mRNA stability by binding to specific mRNA sequences called iron responsive elements (IREs). Murine macrophages were activated with interferon-gamma and lipopolysaccharide to induce NO synthase activity and cultured in the presence or absence of NG-substituted analogues of L-arginine which served as selective inhibitors of NO synthesis. Measurement of the nitrite concentration in the culture medium was taken as an index of NO production. Mitochondria-free cytosols were then prepared and aconitase activity as well as IRE binding activity and induction of IRE binding activity were correlated and depended on NO synthesis after IFN-gamma and/or LPS stimulation. Authentic NO gas as well as the NO-generating compound 3-morpholinosydnonimine (SIN-1) also conversely modulated aconitase and IRE binding activities of purified recombinant IRF. These results provide evidence that endogenously produced NO may modulate the post-transcriptional regulation of genes involved in iron homeostasis and support the hypothesis that the [Fe-S] cluster of IRF mediates iron-dependent regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aconitate Hydratase / metabolism*
  • Adenocarcinoma
  • Amino Acid Oxidoreductases / biosynthesis*
  • Animals
  • Arginine / metabolism
  • Cell Line
  • Cells, Cultured
  • Enzyme Induction
  • Interferon-gamma / pharmacology
  • Iron-Regulatory Proteins
  • Kinetics
  • Leukemia L1210
  • Lipopolysaccharides / pharmacology
  • Macrophage Activation
  • Macrophages, Peritoneal / drug effects
  • Macrophages, Peritoneal / enzymology
  • Macrophages, Peritoneal / metabolism*
  • Mammary Neoplasms, Experimental
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C3H
  • Mitochondria / metabolism
  • Molsidomine / analogs & derivatives
  • Molsidomine / pharmacology
  • Nitric Oxide / biosynthesis*
  • Nitric Oxide / pharmacology
  • Nitric Oxide Synthase
  • Nitrites / metabolism
  • RNA-Binding Proteins / metabolism*
  • Recombinant Proteins / metabolism
  • Tumor Cells, Cultured

Substances

  • Iron-Regulatory Proteins
  • Lipopolysaccharides
  • Nitrites
  • RNA-Binding Proteins
  • Recombinant Proteins
  • Nitric Oxide
  • linsidomine
  • Interferon-gamma
  • Arginine
  • Molsidomine
  • Nitric Oxide Synthase
  • Amino Acid Oxidoreductases
  • Aconitate Hydratase