Barra Melanie M, Richards David M, Hansson Jenny, Hofer Ann-Cathrin, Delacher Michael, Hettinger Jan, Krijgsveld Jeroen, Feuerer Markus
Immune Tolerance, Tumor Immunology Program, German Cancer Research Center, 69120 Heidelberg, Germany; and.
Genome Biology Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
J Immunol. 2015 Oct 1;195(7):3058-70. doi: 10.4049/jimmunol.1500821. Epub 2015 Aug 31.
Regulatory T cells (Tregs) differentiate in the thymus, but the mechanisms that control this process are not fully understood. We generated a comprehensive quantitative and differential proteome of murine Tregs and conventional T cells. We identified 5225 proteins, 164 of which were differentially expressed in Tregs. Together with the comparative analysis of proteome and gene expression data, we identified TCF7 as a promising candidate. Genetic elimination of transcription factor 7 (TCF7) led to increased fractions of Tregs in the thymus. Reduced levels of TCF7, found in the heterozygote, resulted in a greater potential for Treg precursors to differentiate into the Treg lineage. In contrast, activation of TCF7 through β-catenin had the opposite effect. TCF7 levels influenced the required TCR signaling strength of Treg precursors, and TCF7 deficiency broadened the repertoire and allowed lower TCR affinities to be recruited into the Treg lineage. FOXP3 was able to repress TCF7 protein expression. In summary, we propose a regulatory role for TCF7 in limiting access to the Treg lineage.
调节性T细胞(Tregs)在胸腺中分化,但其控制这一过程的机制尚未完全明确。我们生成了小鼠Tregs和常规T细胞的全面定量和差异蛋白质组。我们鉴定出5225种蛋白质,其中164种在Tregs中差异表达。通过蛋白质组和基因表达数据的比较分析,我们确定TCF7是一个有潜力的候选基因。转录因子7(TCF7)的基因敲除导致胸腺中Tregs比例增加。在杂合子中发现的TCF7水平降低,使得Treg前体分化为Treg谱系的潜力更大。相反,通过β-连环蛋白激活TCF7则产生相反的效果。TCF7水平影响Treg前体所需的TCR信号强度,而TCF7缺陷拓宽了TCR库,使更低的TCR亲和力能够被招募到Treg谱系中。FOXP3能够抑制TCF7蛋白表达。总之,我们提出TCF7在限制进入Treg谱系方面具有调节作用。