Proceedings of the National Academy of Sciences · 2005 · 398 citations · 27 references
Life SciencesImmunologyMolecular GeneticsGene ExpressionInflammationTranscriptional RegulationCytokine BiologyInflammatory Cell ResponsesInflammatory Cell SignalingInflammatory MediatorsInflammatory Response RegulationInflammatory SignalingAnti-inflammatory ResponseGene Knock-inInflammatory Mediator InductionInflammatory Response GenesInterleukin-10 Mediated ImmunosuppressionMrna Processing GenesPro-inflammatory Mediator GenesStat3 Signaling
The antiinflammatory cytokine IL-10 inhibits the production of multiple, diverse inflammatory mediators from activated macrophages and dendritic cells, a process requiring STAT3 activation. However, the mechanisms involved in the broad inhibitory effects of IL-10 are controversial. I eliminated the contribution of the major confounding variable to understanding the antiinflammatory response, the 3' UTR region of inflammatory mediator genes, through knock-in mutation and analysis of the effects of IL-10 on transcription rate of inflammatory genes. IL-10 activates STAT3 to act indirectly by selectively inhibiting gene transcription independent of general effects on NF-kappaB or posttranscriptional mRNA processing through a process that reduces the overall transcriptional rate of specific genes.
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IKK-1 and IKK-2: Cytokine-Activated IκB Kinases Essential for NF-κB Activation
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IL-10 acts on the antigen-presenting cell to inhibit cytokine production by Th1 cells
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