Interleukin (IL)-4 is an immunoregulatory cytokine that exerts distinct biological activities on different cell types. Our studies indicate that interferon regulatory factor (IRF)-4 is both a target and a modulator of the IL-4 signaling cascade. IRF-4 expression is strongly upregulated upon costimulation of B cells with CD40 and IL-4. Furthermore, we find that IRF-4 can interact with signal transducer and activator of transcription (Stat)6 and drive the expression of IL-4–inducible genes. The transactivating ability of IRF-4 is blocked by the repressor factor BCL-6. Since expression of IRF-4 is mostly confined to lymphoid cells, these data provide a potential mechanism by which IL-4–inducible genes can be regulated in a lineage-specific manner.
Lineage-Specific Modulation of Interleukin 4 Signaling by Interferon Regulatory Factor 4
Abbreviations used in this paper: BCL-6, B cell lymphomas 6; EMSA, electrophoretic mobility shift assay; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; GAS, IFN-γ–activated site(s); GBP, guanylate binding protein; GSH, glutathione; GST, GSH S-transferase; ICSBP, IFN consensus sequence binding protein; IRF, IFN regulatory factor; ISGF, IFN-stimulated gene factor; ISRE, IFN-stimulated regulatory element; NF-κB, nuclear factor κB; STAT, signal transducer and activator of transcription; WCE, whole cell extract; wt, wild-type.
Sanjay Gupta, Man Jiang, Alissa Anthony, Alessandra B. Pernis; Lineage-Specific Modulation of Interleukin 4 Signaling by Interferon Regulatory Factor 4. J Exp Med 20 December 1999; 190 (12): 1837–1848. doi: https://doi.org/10.1084/jem.190.12.1837
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