The Ubiquitin-like Modifier FAT10 Is Selectively Expressed in Medullary Thymic Epithelial Cells and Modifies T Cell Selection

被引:22
作者
Buerger, Stefanie [1 ]
Herrmann, Valerie L. [1 ]
Mundt, Sarah [1 ]
Trautwein, Nico [2 ]
Groettrup, Marcus [1 ,3 ]
Basler, Michael [1 ,3 ]
机构
[1] Univ Konstanz, Dept Biol, Div Immunol, D-78457 Constance, Germany
[2] Univ Tubingen, Interfac Inst Cell Biol, Dept Immunol, D-72076 Tubingen, Germany
[3] Univ Konstanz, Biotechnol Inst Thurgau, CH-8280 Kreuzlingen, Switzerland
关键词
MHC CLASS-II; TRANSGENIC MICE; PROTEASOMAL DEGRADATION; PROTEIN FAT10; TOLERANCE; VIRUS; ALPHA; GENE; FAT10YLATION; REPERTOIRE;
D O I
10.4049/jimmunol.1500592
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
HLA-F adjacent transcript 10 (FAT10) is a cytokine-inducible ubiquitin-like modifier that is highly expressed in the thymus and directly targets FAT10-conjugated proteins for degradation by the proteasome. High expression of FAT10 in the mouse thymus could be assigned to strongly autoimmune regulator-expressing, mature medullary thymic epithelial cells, which play a pivotal role in negative selection of T cells. Also in the human thymus, FAT10 is localized in the medulla but not the cortex. TCR V beta-segment screening revealed a changed T cell repertoire in FAT10-deficient mice. Analysis of five MHC class I-and II-restricted TCR-transgenic mice demonstrated an altered thymic negative selection in FAT10-deficient mice. Furthermore, the repertoire of peptides eluted from MHC class I molecules was influenced by FAT10 expression. Hence, we identified FAT10 as a novel modifier of thymic Ag presentation and epitope-dependent elimination of self-reactive T cells, which may explain why the fat10 gene could recently be linked to enhanced susceptibility to virus-triggered autoimmune diabetes.
引用
收藏
页码:4106 / 4116
页数:11
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