Tryptophan Metabolism Along the Kynurenine Pathway Downstream of Toll-like Receptor Stimulation in Peripheral Monocytes

Scand J Immunol. 2016 Nov;84(5):262-271. doi: 10.1111/sji.12479.

Abstract

Tryptophan degradation along the kynurenine pathway is of central importance for the immune function. Toll-like receptors (TLRs), representing the first line of immune defence against pathogens, are expressed in various cell types. The most abundant expression is found on monocytes, macrophages and dendritic cells. The aim of this study was to investigate whether stimulation with different TLR ligands induces the kynurenine pathway in human peripheral monocytes. Cell supernatants were analysed using a liquid chromatography/mass spectrometry to measure kynurenine, kynurenic acid (KYNA), quinolinic acid (QUIN) and tryptophan. Stimulation of TLR-2, TLR-3, TLR-4, TLR-7/8 and TLR-9 was found to induce the production of kynurenine, but only stimulation of TLR-3 increased levels of further downstream metabolites, such as KYNA and QUIN. Stimulation of TLR-1, TLR-5 and TLR-6 did not induce the kynurenine pathway. Taken together, this study provides novel evidence demonstrating that TLR activation induces a pattern of downstream tryptophan degradation along the kynurenine pathway in monocytes. The results of this study may implicate that TLRs can be used as new drug targets for the regulation of aberrant tryptophan metabolism along this pathway, a potential therapeutic strategy that may be of importance in several disorders.

MeSH terms

  • Flagellin / pharmacology
  • Gene Expression Regulation
  • Humans
  • Hydrolysis
  • Imidazoles / pharmacology
  • Kynurenic Acid / immunology
  • Kynurenic Acid / metabolism
  • Kynurenine / agonists
  • Kynurenine / immunology*
  • Kynurenine / metabolism
  • Lipopeptides / pharmacology
  • Lipopolysaccharides / pharmacology
  • Listeria monocytogenes / chemistry
  • Monocytes / cytology
  • Monocytes / drug effects
  • Monocytes / immunology*
  • Poly I-C / pharmacology
  • Primary Cell Culture
  • Protein Isoforms / agonists
  • Protein Isoforms / genetics
  • Protein Isoforms / immunology
  • Quinolinic Acid / immunology
  • Quinolinic Acid / metabolism
  • Signal Transduction
  • Toll-Like Receptors / agonists
  • Toll-Like Receptors / genetics
  • Toll-Like Receptors / immunology*
  • Tryptophan / immunology*
  • Tryptophan / metabolism

Substances

  • Imidazoles
  • Lipopeptides
  • Lipopolysaccharides
  • Protein Isoforms
  • Toll-Like Receptors
  • Flagellin
  • Kynurenine
  • Tryptophan
  • Quinolinic Acid
  • Kynurenic Acid
  • Poly I-C
  • resiquimod