Noncanonical NF-κB signaling in dendritic cells is required for indoleamine 2,3-dioxygenase (IDO) induction and immune regulation

被引:129
作者
Tas, Sander W.
Vervoordeldonk, Margriet J.
Hajji, Najat
Schuitemaker, Joost H. N.
van der Sluijs, Koen F.
May, Michael J.
Ghosh, Sankar
Kapsenberg, Martien L.
Tak, Paul P.
de Jong, Esther C.
机构
[1] Univ Amsterdam, Div Clin Immunol & Rheumatol, NL-1100 DD Amsterdam, Netherlands
[2] Univ Amsterdam, Dept Cell Biol & Histol, Acad Med Ctr, NL-1100 DD Amsterdam, Netherlands
[3] Univ Amsterdam, Dept Expt Immunol, Acad Med Ctr, NL-1100 DD Amsterdam, Netherlands
[4] Univ Penn, Sch Vet Med, Dept Biol Anim, Philadelphia, PA 19104 USA
[5] Yale Univ, Sch Med, Immunobiol Sect, New Haven, CT 06520 USA
关键词
D O I
10.1182/blood-2006-11-056010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ligation of CD40 on dendritic cells (DCs) induces early production of inflammatory mediators via canonical NF-kappa B signaling, as well as late expression of the anti inflammatory enzyme indoleamine 2,3dioxygenase (IDO) via unknown signal transduction. By selective blocking of either the canonical NF-kappa B pathway using the NEMO-binding domain peptide or the noncanonical NF-kappa B pathway by small interfering RNA, we demonstrate that IDO expression requires noncanonical NF-kappa B signaling. Also, noncanonical NF-kappa B signaling down-regulates proinflammatory cytokine production in DCs. In addition, selective activation of the noncanonical NF-kappa B pathway results in noninflammatory DCs that suppress T-cell activation and promote the development of T cells with regulatory properties. These findings reveal an important role of the noncanonical NF-kappa B pathway in the regulation of immunity.
引用
收藏
页码:1540 / 1549
页数:10
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