c-Rel but not NF-κB1 is important for T regulatory cell development

被引:55
作者
Deenick, Elissa K. [2 ,3 ]
Elford, Alisha R. [2 ,3 ]
Pellegrini, Marc [2 ,3 ]
Hall, Haken [2 ,3 ]
Mak, Tak W. [2 ,3 ]
Ohashi, Pamela S. [1 ,2 ,3 ]
机构
[1] Ontario Canc Inst, Campbell Family Inst Breast Canc Res, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON, Canada
关键词
NF-kappa B; Regulatory T cells; T cells; Tolerance; NF-KAPPA-B; DIFFERENTIAL REQUIREMENT; PKC-THETA; INTERLEUKIN-2; ACTIVATION; CARMA1; EXPRESSION; MATURE; COSTIMULATION; HOMEOSTASIS;
D O I
10.1002/eji.201040298
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T (Treg) cells are crucial for maintaining peripheral tolerance and controlling T-cell responses. The generation of Treg in the thymus requires TCR triggering and CD28 costimulation. Engagement of these receptors induces a number of signalling pathways, including the activation of NF-kappa B via PKC theta and the Bcl-10/CARMA1/MALT complex. Previous studies have shown that PKC theta, Bcl-10 and CARMA1 are important for Treg development. It is unclear, however, whether different members of the NF-kappa B family contribute to Treg development or homeostasis. In this study, we show that Treg numbers are reduced in the absence of c-Rel but not NF-kappa B1 (p50). Furthermore, using mixed bone marrow chimeras from WT and KO animals, we demonstrate that the requirement for PKC theta, Bcl-10 and c-Rel is T-cell intrinsic, and cannot be rescued by the presence of WT cells. Therefore, c-Rel and NF-kappa B1 have differential roles in Treg development.
引用
收藏
页码:677 / 681
页数:5
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