4.7 Article

Induction of NFATc2 expression by interleukin 6 promotes T helper type 2 differentiation

Journal

JOURNAL OF EXPERIMENTAL MEDICINE
Volume 196, Issue 1, Pages 39-49

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20020026

Keywords

CD4(+) T cells; ILA; NFAT; cytokines; gene regulation

Funding

  1. NCRR NIH HHS [P20 RR015557, P20 RR 15557] Funding Source: Medline
  2. NIAID NIH HHS [P01 AI45666, P01 AI045666] Funding Source: Medline
  3. NIEHS NIH HHS [T32ES07122, T32 ES007122] Funding Source: Medline

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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.

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