IFNα对专业与非专业APCs中MHC II类表达的影响:CIITA IV型启动子的作用

Laura Pisapia , Giovanna Del Pozzo , Pasquale Barba , Alessandra Citro , Paul E. Harris , Antonella Maffei
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引用次数: 6

摘要

我们之前证明,在离体培养中,IFNα下调与胰岛相关的人类非专业apc中MHCII类(MHCII)基因的表达。IFNα对专业APCs中MHCII的表达有相反的作用。本研究发现,在人MHCII阳性非专业抗原提呈的人非造血细胞系中,ifn α-介导的MHCII下调的机制是调节细胞因子信号转导的负反馈系统的结果,最终抑制CIITA基因的启动子III和启动子IV。由于CIITA-PIV亚型主要负责非专业apc中MHCII基因的组成性表达,因此我们在体外系统中追求并实现了CIITA-PIV mRNA的特异性敲低,获得了与IFNα类似的MHCII分子的部分沉默。我们相信我们的结果为CIITA-PIV作为干预策略的治疗靶点的潜在意义提供了新的理解,这些干预策略可以在对免疫系统专业apc功能干扰很小的情况下控制自身免疫性疾病和同种异体移植排斥反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contrasting effects of IFNα on MHC class II expression in professional vs. nonprofessional APCs: Role of CIITA type IV promoter

We previously demonstrated that, in ex vivo cultures, IFNα downregulates the expression of MHC class II (MHCII) genes in human non-professional APCs associated with pancreatic islets. IFNα has an opposing effect on MHCII expression in professional APCs. In this study, we found that the mechanism responsible for the IFNα-mediated MHCII's downregulation in human MHCII-positive non-professional antigen presenting human non-hematopoietic cell lines is the result of the negative feedback system that regulates cytokine signal transduction, which eventually inhibits promoters III and IV of CIITA gene. Because the CIITA-PIV isoform is mostly responsible for the constitutive expression of MHCII genes in non-professional APCs, we pursued and achieved the specific knockdown of CIITA-PIV mRNA in our in vitro system, obtaining a partial silencing of MHCII molecules similar to that obtained by IFNα. We believe that our results offer a new understanding of the potential significance of CIITA-PIV as a therapeutic target for interventional strategies that can manage autoimmune disease and allograft rejection with little interference on the function of professional APCs of the immune system.

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