Immunology Section, Department of Experimental Medical Science, Lund University, 22184 Lund, Sweden.
Translational Disease Systems Biology Program, Novo Nordisk Foundation Center for Protein Research, Copenhagen University, 2200 Copenhagen, Denmark.
J Immunol. 2018 Jul 15;201(2):524-532. doi: 10.4049/jimmunol.1800418. Epub 2018 May 30.
Despite the essential role of thymic epithelial cells (TEC) in T cell development, the signals regulating TEC differentiation and homeostasis remain incompletely understood. In this study, we show a key in vivo role for the vitamin A metabolite, retinoic acid (RA), in TEC homeostasis. In the absence of RA signaling in TEC, cortical TEC (cTEC) and CD80MHC class II medullary TEC displayed subset-specific alterations in gene expression, which in cTEC included genes involved in epithelial proliferation, development, and differentiation. Mice whose TEC were unable to respond to RA showed increased cTEC proliferation, an accumulation of stem cell Ag-1 cTEC, and, in early life, a decrease in medullary TEC numbers. These alterations resulted in reduced thymic cellularity in early life, a reduction in CD4 single-positive and CD8 single-positive numbers in both young and adult mice, and enhanced peripheral CD8 T cell survival upon TCR stimulation. Collectively, our results identify RA as a regulator of TEC homeostasis that is essential for TEC function and normal thymopoiesis.
尽管胸腺上皮细胞(TEC)在 T 细胞发育中起着至关重要的作用,但调节 TEC 分化和稳态的信号仍不完全清楚。在这项研究中,我们显示了维生素 A 代谢物视黄酸(RA)在 TEC 稳态中的关键体内作用。在 TEC 中缺乏 RA 信号的情况下,皮质 TEC(cTEC)和 CD80MHC 类 II 髓质 TEC 显示出亚群特异性的基因表达改变,其中 cTEC 包括参与上皮细胞增殖、发育和分化的基因。TEC 无法对 RA 做出反应的小鼠显示出 cTEC 增殖增加、干细胞 Ag-1 cTEC 积累,并且在生命早期,髓质 TEC 数量减少。这些改变导致生命早期胸腺细胞数量减少,年轻和成年小鼠的 CD4 单阳性和 CD8 单阳性数量减少,TCR 刺激后外周 CD8 T 细胞存活增加。总的来说,我们的结果表明 RA 是 TEC 稳态的调节剂,对 TEC 功能和正常胸腺生成至关重要。