NF-κB-inducing kinase establishes self-tolerance in a thymic stroma-dependent manner

被引:169
作者
Kajiura, F
Sun, S
Nomura, T
Izumi, K
Ueno, T
Bando, Y
Kuroda, N
Han, HW
Li, Y
Matsushima, A
Takahama, Y
Sakaguchi, S
Mitani, T
Matsumoto, M
机构
[1] Univ Tokushima, Div Mol Immunol, Inst Enzyme Res, Tokushima 7708503, Japan
[2] Univ Tokushima, Dept Mol & Environm Pathol, Sch Med, Tokushima 7708503, Japan
[3] Kyoto Univ, Dept Expt Pathol, Inst Frontier Med Sci, Kyoto, Japan
[4] Univ Tokushima, Div Expt Immunol, Inst Genome Res, Tokushima 770, Japan
[5] RIKEN, Res Ctr Allergy & Immunol, Lab Immune Syst Dev, Tokushima, Japan
[6] RIKEN, Res Ctr Allergy & Immunol, Immunopathol Lab, Yokohama, Kanagawa, Japan
关键词
D O I
10.4049/jimmunol.172.4.2067
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Physical contact between thymocytes and the thymic stroma is essential for T cell maturation and shapes the T cell repertoire in the periphery. Stromal elements that control these processes still remain elusive. We used a mouse strain with mutant NF-kappaB inducing kinase (NIK) to examine the mechanisms underlying the breakdown of self-tolerance. This NIK-mutant strain manifests autoimmunity and disorganized thymic structure with abnormal expression of Rel proteins in the stroma. Production of immunoregulatory T cells that control autoreactive T cells was impaired in NIK-mutant mice. The autoimmune disease seen in NIK-mutant mice was reproduced in athymic nude mice by grafting embryonic thymus from NIK-mutant mice, and this was rescued by supply of exogenous immunoregulatory T cells. Impaired production of immunoregulatory T cells by thymic stroma without normal NIK was associated with altered expression of peripheral tissue-restricted Ags, suggesting an essential role of NIK in the thymic microenvironment in the establishment of central tolerance.
引用
收藏
页码:2067 / 2075
页数:9
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