IFN-gamma-induced IDO and WRS expression in microglia is differentially regulated by IL-4

Glia. 2007 Oct;55(13):1385-96. doi: 10.1002/glia.20544.

Abstract

Indoleamine 2,3-dioxygenase (IDO), a tryptophan catabolizing enzyme, has been implicated in the pathogenesis of various neurological disorders. IDO expression is induced by IFN-gamma and leads to neurotoxicity by generating quinolinic acid. Additionally, it inhibits the immune response through both tryptophan depletion and generating other tryptophan catabolites. IL-4 and IL-13 have been shown to control IDO expression by antagonizing the effects of IFN-gamma in different cell types. Here, we investigated the effects of these cytokines on IDO expression in microglia. Interestingly, we observed that both IL-4 and IL-13 greatly enhanced IFN-gamma-induced IDO expression. However, tryptophanyl-tRNA synthetase (WRS), which is coinduced with IDO by IFN-gamma, is downregulated by IL-4 and IL-13. The effect of IL-4 and IL-13 was independent of STAT-6. Modulation of IDO but not WRS was eliminated by inhibition of protein phosphatase 2A (PP2A) activity. The phosphatidylinositol 3-kinase (PI3K) pathway further differentiated the regulation of these two enzymes, as inhibiting the PI3K pathway eliminated IFN-gamma induction of IDO, whereas such inhibition greatly enhanced WRS expression. These findings show discordance between modulations of expression of two distinct enzymes utilizing tryptophan as a common substrate, and raise the possibility of their involvement in regulating immune responses in various neurological disorders.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cells, Cultured
  • Gene Expression / drug effects
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / genetics
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / metabolism*
  • Interferon-gamma / pharmacology*
  • Interleukin-13 / pharmacology
  • Interleukin-4 / pharmacology*
  • Mice
  • Mice, Knockout
  • Microglia / drug effects*
  • Microglia / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoprotein Phosphatases / metabolism
  • Phosphorylation
  • Protein Phosphatase 2
  • STAT1 Transcription Factor / genetics
  • STAT1 Transcription Factor / metabolism
  • STAT1 Transcription Factor / physiology
  • STAT6 Transcription Factor / genetics
  • STAT6 Transcription Factor / physiology
  • Signal Transduction / physiology
  • Tryptophan-tRNA Ligase / genetics
  • Tryptophan-tRNA Ligase / metabolism*

Substances

  • Indoleamine-Pyrrole 2,3,-Dioxygenase
  • Interleukin-13
  • STAT1 Transcription Factor
  • STAT6 Transcription Factor
  • Stat1 protein, mouse
  • Stat6 protein, mouse
  • Interleukin-4
  • Interferon-gamma
  • Phosphatidylinositol 3-Kinases
  • Phosphoprotein Phosphatases
  • Protein Phosphatase 2
  • Tryptophan-tRNA Ligase