IL-18 produced by thymic epithelial cells induces development of dendritic cells with CD11b in the fetal thymus

被引:6
|
作者
Ito, Hiroaki
Esashi, Eiji
Akiyama, Taishin
Inoue, Jun-ichiro
Miyajima, Atsushi
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[2] JST, CREST, Kawaguchi, Japan
[3] Univ Tokyo, Inst Med Sci, Minato Ku, Tokyo 1088639, Japan
基金
日本科学技术振兴机构;
关键词
CD11b; dendritic cells; fetal thymus; IL-18; thymic epithelial cells;
D O I
10.1093/intimm/dxl058
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thymic dendritic cells (DCs) are suggested to be involved in T cell selection; however, their exact origin and function remain to be established. Although DCs in the adult thymus are mostly CD8 alpha(+)CD11b(-), we found that CD8 alpha(-)CD11b(+) DCs were abundantly present in the fetal thymus and they possessed antigen-presenting activity. Interestingly, these CD11b(+) DCs were significantly decreased in mice deficient for TNFR-associated factor 6 (TRAF6), a key signaling molecule downstream of IL-1 and tumor necrosis factor-alpha that have been known to induce DCs from intra-thymic precursor cells. CD11b(+) DCs were induced from CD4(-)CD8(-) thymocytes by fetal thymic epithelial cells (TECs). Analysis of cytokine expression in TECs revealed that none of the cytokines previously shown to induce DCs were expressed. Instead, we found strong expression of IL-18 that transmits signals through TRAF6. IL-18 induced CD11b(+) DCs from CD4(-)CD8(-) thymocytes in vitro, which exhibited strong antigen-presenting activity and formed conjugates with CD4(+)CD8(+) T cells efficiently. Taken together, these results strongly suggest that CD11b(+) DCs are differentiated from CD4(-)CD8(-) thymocytes by IL-18 produced from TECs and that they are involved in T cell selection in the fetal thymus.
引用
收藏
页码:1253 / 1263
页数:11
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