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来自CD4(+)3(-)诱导细胞的RANK信号调节胸腺髓质中表达艾里蛋白的上皮细胞的发育。

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

作者信息

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

机构信息

Medical Research Council Centre for Immune Regulation, Institute for Biomedical Research, University of Birmingham, B15 2TT Birmingham, UK.

出版信息

J Exp Med. 2007 Jun 11;204(6):1267-72. doi: 10.1084/jem.20062497. Epub 2007 May 14.


DOI:10.1084/jem.20062497
PMID:17502664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2118623/
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.

摘要

表达艾里蛋白的髓质胸腺上皮细胞(mTECs)通过表达组织限制性抗原,在清除新出现的具有自身反应特异性的T细胞受体库方面发挥关键作用,从而预防自身免疫。在此,我们证明了一种CD4(+)3(-)诱导细胞群体的新作用,该群体先前与有组织的二级淋巴结构的发育以及T细胞记忆的维持有关,在胸腺中对艾里蛋白介导的杂乱基因表达的功能调节中发挥作用。CD4(+)3(-)细胞在成年胸腺中与mTECs密切相关,在胎儿胸腺中,它们的出现与Aire(+) mTECs的出现存在时间上的关联。我们表明,来自该细胞的RANKL信号促进表达RANK的CD80(-)Aire(-) mTEC祖细胞成熟为CD80(+)Aire(+) mTECs,并且将缺乏RANK的胸腺基质移植到免疫缺陷宿主中会诱发自身免疫。总体而言,我们的数据揭示了导致Aire(+) mTECs产生的细胞和分子机制,并突出了CD4(+)3(-)RANKL(+)诱导细胞在胸腺内自身耐受中以前未被认识的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/341e47df160c/jem2041267f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/81c5909ff717/jem2041267f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/16bbd74c75b7/jem2041267f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/c2139a3bb5fd/jem2041267f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/813f11cc28e7/jem2041267f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/341e47df160c/jem2041267f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/81c5909ff717/jem2041267f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/16bbd74c75b7/jem2041267f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/c2139a3bb5fd/jem2041267f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/813f11cc28e7/jem2041267f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181f/2118623/341e47df160c/jem2041267f05.jpg

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[1]
RANK signals from CD4(+)3(-) inducer cells regulate development of Aire-expressing epithelial cells in the thymic medulla.

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本文引用的文献

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