Differential regulation of indoleamine 2,3-dioxygenase by lipopolysaccharide and interferon gamma in murine bone marrow derived dendritic cells

FEBS Lett. 2007 Apr 3;581(7):1449-56. doi: 10.1016/j.febslet.2007.02.073. Epub 2007 Mar 7.

Abstract

Indoleamine 2,3-dioxygenase (IDO) is a rate-limiting enzyme in the L-tryptophan-kynurenine pathway, which converts an essential amino acid, L-tryptophan, to N-formylkynurenine. The expression of IDO increases when inflammation is induced by wounding, infection or tumor growth. Although recent studies have suggested that IDO expression is up-regulated by IFN-gamma in various cell types and that the induction of IDO can also be mediated through an IFN-gamma-independent mechanism, these mechanisms still remain unknown. In this study, we investigated whether lipopolysaccharide (LPS) induces the expression of IDO through an IFN-gamma-mediated signaling pathway or not. IFN-gamma-induced expression of IDO expression was inhibited only by JAK inhibitor I. However, LPS-induced expression of IDO was inhibited by LY294002 and SP600125 but not by JAK inhibitor I, SB203580, or U0126. These findings clearly indicate that LPS can induce the IDO expression via an IFN-gamma-independent mechanism and PI3 kinase and JNK in the LPS-induced pathway leading to IDO expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anthracenes / pharmacology
  • Bone Marrow Cells / enzymology
  • Butadienes / pharmacology
  • Chromones / pharmacology
  • Dendritic Cells / drug effects
  • Dendritic Cells / enzymology*
  • Dendritic Cells / immunology
  • Gene Expression / drug effects
  • Gene Expression Regulation, Enzymologic*
  • Imidazoles / pharmacology
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / genetics*
  • Interferon-gamma / antagonists & inhibitors
  • Interferon-gamma / pharmacology*
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Janus Kinase 1 / antagonists & inhibitors
  • Janus Kinase 1 / metabolism
  • Lipopolysaccharides / pharmacology*
  • Male
  • Mice
  • Mice, Inbred Strains
  • Morpholines / pharmacology
  • Nitriles / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoinositide-3 Kinase Inhibitors
  • Protein Kinase Inhibitors / pharmacology
  • Pyridines / pharmacology

Substances

  • Anthracenes
  • Butadienes
  • Chromones
  • Imidazoles
  • Indoleamine-Pyrrole 2,3,-Dioxygenase
  • Lipopolysaccharides
  • Morpholines
  • Nitriles
  • Phosphoinositide-3 Kinase Inhibitors
  • Protein Kinase Inhibitors
  • Pyridines
  • U 0126
  • pyrazolanthrone
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • Interferon-gamma
  • Janus Kinase 1
  • JNK Mitogen-Activated Protein Kinases
  • SB 203580