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人类和小鼠模型中自身免疫调节因子调控基因的荟萃分析:一种新型人类模型为自身免疫调节因子在调控信号转导和转录激活因子1(STAT1)及STAT1调控基因中的作用提供见解

Meta-Analysis of Autoimmune Regulator-Regulated Genes in Human and Murine Models: A Novel Human Model Provides Insights on the Role of Autoimmune Regulator in Regulating STAT1 and STAT1-Regulated Genes.

作者信息

Lovewell Thomas R J, McDonagh Andrew J G, Messenger Andrew G, Azzouz Mimoun, Tazi-Ahnini Rachid

机构信息

Department of Infection, Immunity and Cardiovascular Disease, The Medical School, University of Sheffield, Sheffield, United Kingdom.

Department of Dermatology, Royal Hallamshire Hospital, Sheffield, United Kingdom.

出版信息

Front Immunol. 2018 Jun 28;9:1380. doi: 10.3389/fimmu.2018.01380. eCollection 2018.

Abstract

Autoimmune regulator (AIRE) regulates promiscuous expression of tissue-restricted antigens in medullary epithelial cells (mTEC) of the thymus. To understand the diverse effects of AIRE, it is crucial to elucidate the molecular mechanisms underlying the process of AIRE-regulated gene expression. In this study, we generated a recombinant AIRE expression variant of the TEC 1A3 human cell line, TEC 1A3 AIRE, to determine genes targeted by AIRE, and using microarray analysis, we identified 482 genes showing significant differential expression ( < 0.05; false discovery rate <5%), with 353 upregulated and 129 downregulated by AIRE expression. Microarray data were validated by quantitative PCR, confirming the differential expression of 12 known AIRE-regulated genes. Comparison of AIRE-dependent differential expression in our cell line model with murine datasets identified 447 conserved genes with a number of transcription regulatory interactions, forming several key nodes, including STAT1, which had over 30 interactions with other AIRE-regulated genes. As STAT1 mutations cause dominant chronic mucocutaneous candidiasis and decreased STAT1 levels in monocytes of autoimmune polyglandular syndrome 1 (APS-1) patients, it was important to further characterize AIRE-STAT1 interactions. TEC 1A3AIRE were treated with the STAT1 phosphorylation inhibitors fludarabine and LLL3 showed that phosphorylated STAT1 (p-STAT1) was not responsible for any of the observed differential expression. Moreover, treatment of TEC 1A3 AIRE with STAT1 shRNA did not induce any significant variation in the expression of unphosphorylated STAT1 (U-STAT1) downstream genes, suggesting that these genes were directly regulated by AIRE but not U-STAT1. The novel model system we have developed provides potential opportunities for further analysis of the pathogenesis of (APS-1) and the wider roles of the AIRE gene.

摘要

自身免疫调节因子(AIRE)可调节胸腺髓质上皮细胞(mTEC)中组织限制性抗原的杂乱表达。为了解AIRE的多种作用,阐明AIRE调节基因表达过程的分子机制至关重要。在本研究中,我们构建了TEC 1A3人细胞系的重组AIRE表达变体TEC 1A3 AIRE,以确定AIRE靶向的基因,并通过微阵列分析,我们鉴定出482个显示出显著差异表达的基因(<0.05;错误发现率<5%),其中353个基因在AIRE表达时上调,129个基因下调。微阵列数据通过定量PCR验证,证实了12个已知的AIRE调节基因的差异表达。将我们细胞系模型中AIRE依赖性差异表达与小鼠数据集进行比较,鉴定出447个保守基因,这些基因存在大量转录调控相互作用,形成了几个关键节点,包括STAT1,它与其他AIRE调节基因有超过30种相互作用。由于STAT1突变会导致显性慢性黏膜皮肤念珠菌病,且自身免疫性多腺体综合征1型(APS - 1)患者单核细胞中STAT1水平降低,因此进一步表征AIRE - STAT1相互作用很重要。用STAT1磷酸化抑制剂氟达拉滨和LLL3处理TEC 1A3AIRE表明,磷酸化的STAT1(p - STAT1)与任何观察到的差异表达无关。此外,用STAT1 shRNA处理TEC 1A3 AIRE并未诱导未磷酸化的STAT1(U - STAT1)下游基因表达出现任何显著变化,这表明这些基因是由AIRE直接调节的,而非U - STAT1。我们开发的新型模型系统为进一步分析(APS - 1)的发病机制以及AIRE基因更广泛的作用提供了潜在机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18b3/6031710/85fda39156f1/fimmu-09-01380-g001.jpg

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