Interleukin (IL)-6 is produced by professional antigen-presenting cells (APCs) such as B cells, macrophages, and dendritic cells. It has been previously shown that APC-derived IL-6 promotes the differentiation of naive CD4+ T cells into effector T helper type 2 (Th2) cells. Here, we have studied the molecular mechanism for IL-6–mediated Th2 differentiation. During the activation of CD4+ T cells, IL-6 induces the production of IL-4, which promotes the differentiation of these cells into effector Th2 cells. Regulation of IL-4 gene expression by IL-6 is mediated by nuclear factor of activated T cells (NFAT), as inhibition of NFAT prevents IL-6–driven IL-4 production and Th2 differentiation. IL-6 upregulates NFAT transcriptional activity by increasing the levels of NFATc2. The ability of IL-6 to promote Th2 differentiation is impaired in CD4+ T cells that lack NFATc2, demonstrating that NFATc2 is required for regulation of IL-4 gene expression by IL-6. Regulation of NFATc2 expression and NFAT transcriptional activity represents a novel pathway by which IL-6 can modulate gene expression.
Induction of NFATc2 Expression by Interleukin 6 Promotes T Helper Type 2 Differentiation
C.-W. Chow's present address is Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY 10461.
Abbreviations used in this paper: AP-1, activator protein 1; C/EBP, CCAAT/enhancer binding protein; CREB, cAMP element binding protein; EMSA, electrophoretic mobility shift assay; JAK, Janus kinase; NFAT, nuclear factor of activated T cells; RPA, ribonuclease protection assay; STAT, signal transducer and activator of transcription.
Sean Diehl, Chi-Wing Chow, Linda Weiss, Alois Palmetshofer, Thomas Twardzik, Laura Rounds, Edgar Serfling, Roger J. Davis, Juan Anguita, Mercedes Rincón; Induction of NFATc2 Expression by Interleukin 6 Promotes T Helper Type 2 Differentiation . J Exp Med 1 July 2002; 196 (1): 39–49. doi: https://doi.org/10.1084/jem.20020026
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