Nature Immunology · 2011 · 690 citations · 34 references
Life SciencesImmunologyMolecular BiologyCell SignalingImmunoregulationSignal TransductionDendritic Cell BiologyDendritic Cell RegulationDendritic FunctionInflammatory SignalingNeuroimmune ToleranceDendritic Cell Immune ToleranceDendritic Cell SignalingDendritic Cell Tolerance InductionDendritic Cell Tolerogenic FunctionDendritic Cell TolerogenicityIndoleamine 2, 3-Dioxygenase PathwayTolerogenic Dendritic Cells
The tryptophan-catalytic activity of IDO in dendritic cells is known to regulate immune responses. Grohmann and co-workers show that IDO also functions as an intracellular signal transducer in response to transforming growth factor-β. Regulation of tryptophan metabolism by indoleamine 2,3-dioxygenase (IDO) in dendritic cells (DCs) is a highly versatile modulator of immunity. In inflammation, interferon-γ is the main inducer of IDO for the prevention of hyperinflammatory responses, yet IDO is also responsible for self-tolerance effects in the longer term. Here we show that treatment of mouse plasmacytoid DCs (pDCs) with transforming growth factor-β (TGF-β) conferred regulatory effects on IDO that were mechanistically separable from its enzymic activity. We found that IDO was involved in intracellular signaling events responsible for the self-amplification and maintenance of a stably regulatory phenotype in pDCs. Thus, IDO has a tonic, nonenzymic function that contributes to TGF-β-driven tolerance in noninflammatory contexts.
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Prevention of Allogeneic Fetal Rejection by Tryptophan Catabolism
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