Division of Molecular Immunology, Institute for Enzyme Research, University of Tokushima, Tokushima 770-8503, Japan;
J Immunol. 2014 Mar 15;192(6):2585-92. doi: 10.4049/jimmunol.1302786. Epub 2014 Feb 10.
Understanding the cellular dynamics of Aire-expressing lineage(s) among medullary thymic epithelial cells (AEL-mTECs) is essential for gaining insight into the roles of Aire in establishment of self-tolerance. In this study, we monitored the maturation program of AEL-mTECs by temporal lineage tracing, in which bacterial artificial chromosome transgenic mice expressing tamoxifen-inducible Cre recombinase under control of the Aire regulatory element were crossed with reporter strains. We estimated that the half-life of AEL-mTECs subsequent to Aire expression was ∼7-8 d, which was much longer than that reported previously, owing to the existence of a post-Aire stage. We found that loss of Aire did not alter the overall lifespan of AEL-mTECs, inconsistent with the previous notion that Aire expression in medullary thymic epithelial cells (mTECs) might result in their apoptosis for efficient cross-presentation of self-antigens expressed by AEL-mTECs. In contrast, Aire was required for the full maturation program of AEL-mTECs, as exemplified by the lack of physiological downregulation of CD80 during the post-Aire stage in Aire-deficient mice, thus accounting for the abnormally increased CD80(high) mTECs seen in such mice. Of interest, increased CD80(high) mTECs in Aire-deficient mice were not mTEC autonomous and were dependent on cross-talk with thymocytes. These results further support the roles of Aire in the differentiation program of AEL-mTECs.
理解表达 Aire 的细胞谱系(系)在骨髓胸腺上皮细胞(AEL-mTECs)中的细胞动力学对于深入了解 Aire 在建立自身耐受中的作用至关重要。在这项研究中,我们通过时间谱系追踪监测 AEL-mTEC 成熟程序,其中细菌人工染色体转基因小鼠在 Aire 调节元件的控制下表达他莫昔芬诱导的 Cre 重组酶,并与报告株系杂交。我们估计 Aire 表达后 AEL-mTEC 的半衰期约为 7-8 天,这比以前报道的要长得多,因为存在 Aire 后阶段。我们发现 Aire 的缺失不会改变 AEL-mTEC 的总体寿命,这与之前的观点不一致,即髓质胸腺上皮细胞(mTECs)中的 Aire 表达可能导致它们凋亡,以有效交叉呈递 AEL-mTEC 表达的自身抗原。相反,Aire 是 AEL-mTEC 完全成熟程序所必需的,例如在 Aire 缺陷型小鼠中,在 Aire 后阶段缺乏 CD80 的生理下调,从而解释了在这些小鼠中看到的异常增加的 CD80(high) mTEC。有趣的是,Aire 缺陷型小鼠中增加的 CD80(high) mTEC 不是 mTEC 自主的,而是依赖于与胸腺细胞的交叉对话。这些结果进一步支持了 Aire 在 AEL-mTEC 分化程序中的作用。