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

Simona W. Rossi(Immune Regulation (United Kingdom)), Mi‐Yeon Kim(Immune Regulation (United Kingdom)), Andreas Leibbrandt(Institute of Molecular Biotechnology), Sonia M. Parnell(Immune Regulation (United Kingdom)), William E. Jenkinson(Immune Regulation (United Kingdom)), Stephanie H. Glanville(Immune Regulation (United Kingdom)), Fiona M. McConnell(Immune Regulation (United Kingdom)), Hamish S. Scott(Walter and Eliza Hall Institute of Medical Research), Josef Penninger(Institute of Molecular Biotechnology), Eric J. Jenkinson(Immune Regulation (United Kingdom)), Peter J. L. Lane(Immune Regulation (United Kingdom)), Graham Anderson(Immune Regulation (United Kingdom))
The Journal of Experimental Medicine
May 14, 2007
Cited by 479Open Access
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Abstract

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.


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