IL-6-dependent and -independent pathways in the development of interleukin 17-producing T helper cells

被引:292
|
作者
Kimura, Akihiro
Naka, Tetsuji
Kishimoto, Tadamitsu
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Lab Immune Regulat, Suita, Osaka 565, Japan
[2] Natl Inst Biomed Innovat, Lab Immune Signal, Ibaraki 5670085, Japan
关键词
STAT; TGF-beta; retinoid-related orphan receptor gamma t; regulatory T cells;
D O I
10.1073/pnas.0705268104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CD4(+) T cells producing IL-17 [T helper (Th)17], as distinct from Thl or Th2 cells, have recently been shown to be associated with autoimmunity, but it is not entirely clear how Th17 cells are generated from naive T cells. We demonstrate here that IL-6, but not TNF-alpha or IL-1 beta, can, in combination with TGF-beta, induce Th17 cell generation from naive T cells and inhibit TGF-beta-induced Foxp3 expression. Moreover, conditioned medium from lipopolysaccharide-stimulated bone marrow-derived dendritic cells (DCCM) can induce IL-17 production in naive T cells. Interestingly, IL-17 was produced by DCCM even with the addition of anti-gp 130 antibody or DCCM from IL-6 KO mice. The combination of IL-6 and TGF-P could maintain activation of signal transducer and activator of transcription (Stat)3, but not of Stat1. IL-27 or IFN-gamma suppressed the induction of Th17 cells by TGF-P plus IL-6 and maintained Stat1 activation under these conditions. In contrast, both Stat1 and Stat3 remained to be activated in naive T cells cultured with DCCM. These findings represent a different basis for Th17 differentiation from naive T cells.
引用
收藏
页码:12099 / 12104
页数:6
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