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Activation of interleukin-6 gene expression through the NF-kappa B transcription factor.
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1990
Year
Immune RegulationImmunologyImmune SystemInflammationIl-6 PromoterTranscriptional RegulationProtein ExpressionNf-kb Signaling PathwayImmune MediatorCell SignalingInflammatory ResponseInterleukin-6 Gene ExpressionGene ExpressionIl-6 GeneCell BiologyTranscription RegulationCytokineSignal TransductionGene RegulationMedicine
The IL‑6 promoter contains a putative NF‑κB binding site, and NF‑κB is a key regulator of inflammatory genes, suggesting a central role in infection and tissue injury responses. Binding of NF‑κB to the IL‑6 promoter is required for inducible promoter activity; mutation of the site abolishes binding and blocks induction by various stimuli in U‑937 and HeLa cells, indicating NF‑κB is a major mediator of IL‑6 gene activation while other enhancer elements contribute in a cell‑specific manner.
The promoter region of the interleukin-6 (IL-6) gene has a putative NF-kappa B-binding site. We found that a fragment of the IL-6 promoter containing the site specifically binds highly purified NF-kappa B protein and the NF-kappa B protein in nuclear extracts of phorbol ester-induced Jurkat cells. Mutations of the NF-kappa B site abolished complex formation with both purified NF-kappa B and the nuclear extract protein. Transient expression of chloramphenicol acetyltransferase (CAT) plasmids containing the IL-6 promoter revealed very little activity of the promoter in U-937 monocytic cells and in HeLa cells before stimulation. However, stimulation of U-937 and HeLa cells by inducers of NF-kappa B led to a dramatic increase in CAT activity. Mutations in the NF-kappa B-binding site abolished inducibility of IL-6 promoter-cat constructs in U-937 cells by lipopolysaccharide, tumor necrosis factor alpha, the double-stranded RNA poly(IC), or phytohemagglutinin and in HeLa cells by tumor necrosis factor alpha and drastically reduced but did not completely eliminate inducibility in HeLa cells stimulated by double-stranded RNA poly(IC) or phorbol 12-myristate 13-acetate. These results suggest that NF-kappa B is an important mediator for activation of the IL-6 gene by a variety of IL-6 inducers in both U-937 and HeLa cells and that alternative inducible enhancer elements contribute in a cell-specific manner to IL-6 gene induction. Because NF-kappa B is involved in the control of a variety of genes activated upon inflammation, NF-kappa B may play a central role in the inflammatory response to infection and tissue injury.
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