Division of Molecular Immunology, Institute for Enzyme Research, Tokushima University, Tokushima, Japan.
Japan Agency for Medical Research and Development-Core Research for Evolutional Science and Technology, Tokyo, Japan.
Eur J Immunol. 2015 Dec;45(12):3237-40. doi: 10.1002/eji.201546098.
Aire has been cloned as the gene responsible for a hereditary type of organ-specific autoimmune disease. Aire controls the expression of a wide array of tissue-restricted Ags by medullary thymic epithelial cells (mTECs), thereby leading to clonal deletion and Treg-cell production, and ultimately to the establishment of self-tolerance. However, relatively little is known about the mechanism responsible for the control of Aire expression itself. In this issue of the European Journal of Immunology, Haljasorg et al. [Eur. J. Immunol. 2015. 45: 3246-3256] have reported the presence of an enhancer element for Aire that binds with NF-κB components downstream of the TNF receptor family member, RANK (receptor activator of NF-κB). The results suggest that RANK has a dual mode of action in Aire expression: one involving the promotion of mTEC differentiation and the other involving activation of the molecular switch for Aire within mature mTECs.
Aire 已被克隆为一种遗传性器官特异性自身免疫疾病的相关基因。Aire 通过髓质胸腺上皮细胞 (mTEC) 控制多种组织特异性抗原的表达,从而导致克隆性删除和 Treg 细胞产生,并最终建立自身耐受。然而,对于负责 Aire 表达本身的调控机制,我们知之甚少。在本期《欧洲免疫学杂志》中,Haljasorg 等人 [Eur. J. Immunol. 2015. 45: 3246-3256] 报道了一个 Aire 的增强子元件,该元件与 TNF 受体家族成员 RANK(NF-κB 受体激活物)下游的 NF-κB 成分结合。这些结果表明,RANK 在 Aire 表达中具有双重作用模式:一种涉及促进 mTEC 分化,另一种涉及激活成熟 mTEC 中 Aire 的分子开关。