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

被引:156
作者
Diehl, S
Chow, CW
Weiss, L
Palmetshofer, A
Twardzik, T
Rounds, L
Serfling, E
Davis, RJ
Anguita, J
Rincón, M
机构
[1] Univ Vermont, Dept Med, Immunobiol Program, Burlington, VT 05405 USA
[2] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Worcester, MA 01605 USA
[3] Univ Massachusetts, Sch Med, Dept Biochem & Mol Biol, Program Mol Med, Worcester, MA 01605 USA
[4] Univ N Carolina, Dept Biol, Charlotte, NC 28223 USA
[5] Univ Wurzburg, Inst Pathol, Dept Mol Pathol, D-97080 Wurzburg, Germany
关键词
CD4(+) T cells; ILA; NFAT; cytokines; gene regulation;
D O I
10.1084/jem.20020026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
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.
引用
收藏
页码:39 / 49
页数:11
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