Protein tyrosine nitration in cytokine-activated murine macrophages. Involvement of a peroxidase/nitrite pathway rather than peroxynitrite

J Biol Chem. 2001 Sep 7;276(36):34051-8. doi: 10.1074/jbc.M100585200. Epub 2001 Jun 25.

Abstract

Peroxynitrite, formed in a rapid reaction of nitric oxide (NO) and superoxide anion radical (O(2)), is thought to mediate protein tyrosine nitration in various inflammatory and infectious diseases. However, a recent in vitro study indicated that peroxynitrite exhibits poor nitrating efficiency at biologically relevant steady-state concentrations (Pfeiffer, S., Schmidt, K., and Mayer, B. (2000) J. Biol. Chem. 275, 6346-6352). To investigate the molecular mechanism of protein tyrosine nitration in intact cells, murine RAW 264.7 macrophages were activated with immunological stimuli, causing inducible NO synthase expression (interferon-gamma in combination with either lipopolysaccharide or zymosan A), followed by the determination of protein-bound 3-nitrotyrosine levels and release of potential triggers of nitration (NO, O(2)*, H(2)O(2), peroxynitrite, and nitrite). Levels of 3-nitrotyrosine started to increase at 16-18 h and exhibited a maximum at 20-24 h post-stimulation. Formation of O(2) was maximal at 1-5 h and decreased to base line 5 h after stimulation. Release of NO peaked at approximately 6 and approximately 9 h after stimulation with interferon-gamma/lipopolysaccharide and interferon-gamma/zymosan A, respectively, followed by a rapid decline to base line within the next 4 h. NO formation resulted in accumulation of nitrite, which leveled off at about 50 microm 15 h post-stimulation. Significant release of peroxynitrite was detectable only upon treatment of cytokine-activated cells with phorbol 12-myristate-13-acetate, which led to a 2.2-fold increase in dihydrorhodamine oxidation without significantly increasing the levels of 3-nitrotyrosine. Tyrosine nitration was inhibited by azide and catalase and mimicked by incubation of unstimulated cells with nitrite. Together with the striking discrepancy in the time course of NO/O(2) release versus 3-nitrotyrosine formation, these results suggest that protein tyrosine nitration in activated macrophages is caused by a nitrite-dependent peroxidase reaction rather than peroxynitrite.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cytokines / metabolism*
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Inhibitors / pharmacology
  • Free Radical Scavengers / pharmacology
  • Hydrogen Peroxide / metabolism
  • Immunoblotting
  • Interferon-gamma / pharmacology
  • Lipopolysaccharides / pharmacology
  • Macrophages / metabolism*
  • Mice
  • Nitrates / metabolism
  • Nitric Oxide / metabolism
  • Nitrites / metabolism
  • Nitrogen / metabolism*
  • Oxygen / metabolism
  • Peroxidase / antagonists & inhibitors
  • Recombinant Proteins / metabolism
  • Tetradecanoylphorbol Acetate / metabolism
  • Time Factors
  • Tyrosine / analogs & derivatives*
  • Tyrosine / metabolism*
  • Zymosan / pharmacology

Substances

  • Cytokines
  • Enzyme Inhibitors
  • Free Radical Scavengers
  • Lipopolysaccharides
  • Nitrates
  • Nitrites
  • Recombinant Proteins
  • peroxynitric acid
  • Nitric Oxide
  • 3-nitrotyrosine
  • Tyrosine
  • Interferon-gamma
  • Zymosan
  • Hydrogen Peroxide
  • Peroxidase
  • Nitrogen
  • Tetradecanoylphorbol Acetate
  • Oxygen