The signal transducer and activator of transcription 1alpha and interferon regulatory factor 1 are not essential for the induction of indoleamine 2,3-dioxygenase by lipopolysaccharide: involvement of p38 mitogen-activated protein kinase and nuclear factor-kappaB pathways, and synergistic effect of several proinflammatory cytokines

J Biochem. 2006 Apr;139(4):655-62. doi: 10.1093/jb/mvj072.

Abstract

Indoleamine 2,3-dioxygenase (IDO) is induced by interferon (IFN)-gamma-mediated effects of the signal transducer and activator of transcription 1alpha (STAT1alpha) and interferon regulatory factor (IRF)-1. The induction of IDO can also be mediated through an IFN-gamma-independent mechanism, although the mechanism of induction has not been identified. In this study, we explored whether lipopolysaccharide (LPS) or several proinflammatory cytokines can induce IDO via an IFN-gamma-independent mechanism, and whether IDO induction by LPS requires the STAT1alpha and IRF-1 signaling pathways. IDO was induced by LPS or IFN-gamma in peripheral blood mononuclear cells and THP-1 cells, and a synergistic IDO induction occurred when THP-1 cells were cultured in the presence of a combination of tumor necrosis factor-alpha, interleukin-6 or interleukin-1beta. An electrophoretic mobility shift assay using STAT1alpha and IRF-1 consensus oligonucleotide probes showed no STAT1alpha or IRF-1 binding activities in LPS-stimulated THP-1 cells. Further, the LPS-induced IDO activity was inhibited by both p38 mitogen-activated protein kinase (MAPK) and nuclear factor-kappaB (NF-kappaB) inhibitors. These findings suggest that the induction of IDO by LPS in THP-1 cells is not regulated by IFN-gamma via recruitment of STAT1alpha or IRF-1 to the intracellular signaling pathway, and may be related to the activity of the p38 MAPK pathway and NF-kappaB.

MeSH terms

  • Cell Line
  • Cell Line, Tumor
  • Cytokines / pharmacology
  • Electrophoretic Mobility Shift Assay
  • Enzyme Activation / drug effects
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / metabolism*
  • Interferon Regulatory Factor-1 / metabolism*
  • Interferon Regulatory Factor-1 / physiology
  • Interferon-gamma / pharmacology
  • Lipopolysaccharides / pharmacology*
  • Models, Biological
  • NF-kappa B / metabolism*
  • NF-kappa B / physiology
  • STAT1 Transcription Factor / metabolism*
  • STAT1 Transcription Factor / physiology
  • Tumor Necrosis Factor-alpha / pharmacology
  • U937 Cells
  • p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • p38 Mitogen-Activated Protein Kinases / metabolism*
  • p38 Mitogen-Activated Protein Kinases / physiology

Substances

  • Cytokines
  • Enzyme Inhibitors
  • Indoleamine-Pyrrole 2,3,-Dioxygenase
  • Interferon Regulatory Factor-1
  • Lipopolysaccharides
  • NF-kappa B
  • STAT1 Transcription Factor
  • TNF protein, human
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma
  • p38 Mitogen-Activated Protein Kinases