RANK signals from CD4+3- inducer cells regulate development of Aire-expressing epithelial cells in the thymic medulla

被引:381
作者
Rossi, Simona W.
Kim, Mi-Yeon
Leibbrandt, Andreas
Parnell, Sonia M.
Jenkinson, William E.
Glanville, Stephanie H.
McConnell, Fiona M.
Scott, Hamish S.
Penninger, Josef M.
Jenkinson, Eric J.
Lane, Peter J. L.
Anderson, Graham [1 ]
机构
[1] Univ Birmingham, Med Res Council Ctr Immune Regulat, Biomed Res Inst, Birmingham B15 2TT, W Midlands, England
[2] Austrian Acad Sci, Inst Mol Biotechnol, A-1030 Vienna, Austria
[3] Walter & Eliza Hall Inst Med Res, Div Mol Med, Parkville, Vic 3050, Australia
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1084/jem.20062497
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aire-expressing medullary thymic epithelial cells (mTECs) play a key role in preventing autoimmunity by expressing tissue-restricted antigens to help purge the emerging T cell receptor repertoire of self-reactive specificities. Here we demonstrate a novel role for a CD4(+)3(-) inducer cell population, previously linked to development of organized secondary lymphoid structures and maintenance of T cell memory in the functional regulation of Aire-mediated promiscuous gene expression in the thymus. CD4(+)3(-) cells are closely associated with mTECs in adult thymus, and in fetal thymus their appearance is temporally linked with the appearance of Aire(+) mTECs. We show that RANKL signals from this cell promote the maturation of RANK-expressing CD80(-) Aire(-) mTEC progenitors into CD80(+) Aire(+) mTECs, and that transplantation of RANK-deficient thymic stroma into immunodeficient hosts induces autoimmunity. Collectively, our data reveal cellular and molecular mechanisms leading to the generation of Aire+ mTECs and highlight a previously unrecognized role for CD4(+)3(-) RANKL(+) inducer cells in intrathymic self-tolerance.
引用
收藏
页码:1267 / 1272
页数:6
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