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Fezf2 Orchestrates a Thymic Program of Self-Antigen Expression for Immune Tolerance

机译:Fezf2编排胸腺程序的自身抗原表达的免疫耐受。

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Self-tolerance to immune reactions is established via promiscuous expression of tissue-restricted antigens (TRAs) in medullary thymic epithelial cells (mTECs), leading to the elimination of T cells that respond to self-antigens. The transcriptional regulator Aire has been thought to be sufficient for the induction of TRAs, despite some indications that other factors may promote TRA expression in the thymus. Here, we show that the transcription factor Fezf2 directly regulates various TRA genes in mTECs independently of Aire. Mice lacking Fezf2 in mTECs displayed severe autoimmune symptoms, including the production of autoantibodies and inflammatory cell infiltration targeted to peripheral organs. These responses differed from those detected in Aire-deficient mice. Furthermore, Fezf2 expression and Aire expression are regulated by distinct signaling pathways and promote the expression of different classes of proteins. Thus, two independent factors, Fezf2 and Aire, permit the expression of TRAs in the thymus to ensure immune tolerance.
机译:通过在胸腺髓样上皮细胞(mTECs)中组织限制性抗原(TRAs)的混杂表达来建立对免疫反应的自我耐受性,从而消除了对自身抗原作出反应的T细胞的消除。尽管有迹象表明其他因素可能会促进胸腺中TRA的表达,但转录调节因子Aire被认为足以诱导TRAs。在这里,我们表明转录因子Fezf2独立于Aire直接调节mTECs中的各种TRA基因。在mTECs中缺乏Fezf2的小鼠表现出严重的自身免疫症状,包括自身抗体的产生和针对周围器官的炎性细胞浸润。这些反应不同于在Aire缺陷小鼠中检测到的反应。此外,Fezf2表达和Aire表达受不同的信号传导途径调控,并促进不同类别蛋白质的表达。因此,两个独立的因子Fezf2和Aire允许TRAs在胸腺中表达以确保免疫耐受。

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