Curcumin induces the tolerogenic dendritic cell that promotes differentiation of intestine-protective regulatory T cells

被引:76
作者
Cong, Yingzi [1 ]
Wang, Lanfang [1 ]
Konrad, Astrid [1 ]
Schoeb, Trenton [2 ]
Elson, Charles O. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Med, Div Gastroenterol & Hepatol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Human Genet, Birmingham, AL 35294 USA
关键词
Colitis; Curcumin; DC; Foxp3; Treg; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; INFLAMMATORY-BOWEL-DISEASE; NF-KAPPA-B; LAMINA-PROPRIA; ORAL TOLERANCE; EXPRESS FOXP3; GUT BACTERIA; IN-VIVO; GENERATION; INDUCTION;
D O I
10.1002/eji.200939052
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The gut is home to a large number of Treg, with both CD4(+) CD25(+) Treg and bacterial antigen-specific Tr1 cells present in normal mouse intestinal lamina propria. it has been shown recently that intestinal mucosal DC are able to induce Foxp3(+) Treg through production of TGF-beta plus retinoic acid (RA). However, the factors instructing DC toward this mucosal phenotype are currently unknown. Curcumin has been shown to possess a number of biologic activities including the inhibition of NF-kappa B signaling. We asked whether curcumin could modulate DC to be tolerogenic whose function could mimic mucosal DC. We report here that curcumin modulated BM-derived DC to express ALDH1a and IL-10. These curcumin-treated DC induced differentiation of naive CD4(+) T cells into Treg resembling Treg in the intestine, including both CD4(+)CD25(+) Foxp3(+) Treg and IL-10-producing Tr1 cells. Such Treg induction required IL-10, TGF-beta and retinoic acid produced by curcumin-modulated DC. Cell contact as well as IL-10 and TGF-beta production were involved in the function of such induced Treg. More importantly, these Treg inhibited antigen-specific T-cell activation in vitro and inhibited colitis due to antigen-specific pathogenic T cells in vivo.
引用
收藏
页码:3134 / 3146
页数:13
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