Buerger Stefanie, Herrmann Valerie L, Mundt Sarah, Trautwein Nico, Groettrup Marcus, Basler Michael
Division of Immunology, Department of Biology, University of Konstanz, D-78457 Konstanz, Germany;
Department of Immunology, Interfaculty Institute for Cell Biology, University of Tübingen, D-72076 Tübingen, Germany; and.
J Immunol. 2015 Nov 1;195(9):4106-16. doi: 10.4049/jimmunol.1500592. Epub 2015 Sep 23.
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 Vβ-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.
HLA - F相邻转录本10(FAT10)是一种细胞因子诱导的类泛素修饰因子,在胸腺中高表达,并直接将与FAT10缀合的蛋白质靶向蛋白酶体进行降解。FAT10在小鼠胸腺中的高表达可归因于高表达自身免疫调节因子的成熟髓质胸腺上皮细胞,这些细胞在T细胞的阴性选择中起关键作用。在人类胸腺中,FAT10也定位于髓质而非皮质。TCR Vβ片段筛选显示FAT10缺陷小鼠的T细胞库发生了变化。对五只MHC I类和II类限制性TCR转基因小鼠的分析表明,FAT10缺陷小鼠的胸腺阴性选择发生了改变。此外,从MHC I类分子洗脱的肽库受FAT10表达的影响。因此,我们将FAT10鉴定为胸腺抗原呈递和自身反应性T细胞表位依赖性清除的新型修饰因子,这可能解释了为什么最近fat10基因与病毒引发的自身免疫性糖尿病易感性增强有关。