系统性硬化症患者外周血单个核细胞中IRF7和STAT1基因表达谱

R. Rezaei, H. Kavosi, F. Gharibdoost, Hanieh Mojtahedi, M. Vodjgani, M. Mahmoudi
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引用次数: 0

摘要

IFN标志基因在确定系统性硬化症(SSc)的病因和发病机制方面的关键作用已被越来越多地研究。干扰素调节因子(IRFs)和信号转导及转录激活因子(STATs)主要被认为是ifn信号基因和I型干扰素的转录调节剂,在免疫应答的许多方面发挥重要作用。本研究旨在评估硬皮病患者pbmc中IRF7(干扰素调节因子7)和STAT1(信号转导和转录激活因子1)mrna的转录水平,并将其与健康受试者进行比较。在这项研究中,从50名硬皮病患者和30名健康个体中获得pbmc。随后,从分离的PBMCs中提取总RNA并进行cDNA合成。采用实时荧光定量PCR、SYBR Green法和IRF7和STAT1特异性引物检测IRF7和STAT1 mRNA表达。与对照组相比,患者组IRF7的相对表达量明显升高。此外,IRF7在局限性SSc (lSSc)和弥漫性SSc (dSSc)中的相对表达量较健康者显著升高(p< 0.05)。STAT1转录本在PBMCs中的相对表达量在患者组和对照组之间无统计学差异。IRF7的表达与疾病的Rodnan评分(RS)有显著的相关性。考虑到IRF7在SSc患者中过表达,且IRF7与疾病的Rodnan评分有显著相关性,提示IRF7表达受损参与了SSc的发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IRF7 and STAT1 gene expression profile in peripheral blood mononuclear cells of patients with systemic sclerosis
The critical role of IFN signature genes has increasingly been surveyed to determine the etiology and pathogenesis of systemicsclerosis (SSc). Interferon-regulatory factors (IRFs) and signal transducers and activators of transcription (STATs) are mainlyconsidered as transcriptional modulators of IFN-signature genes and type I interferon and play a major role in the regulation ofnumerous aspects of an immune response. The current study aimed to assess the transcriptional levels of IRF7 (interferonregulatory factor 7) and STAT1 (signal transducers and activators of transcription 1) mRNAs in PBMCs of scleroderma patientsand compare them with those of healthy subjects.In this study, PBMCs were obtained from 50 scleroderma patients and 30 healthy individuals. Subsequently, total RNA wasextracted from isolated PBMCs and cDNA synthesis was carried out. IRF7 and STAT1 mRNA expressions were assessed byapplying quantitative real-time PCR, SYBR Green method, and specific primers for IRF7 and STAT1.Relative expression of IRF7 was significantly increased in the patient group compared with the control group. Moreover, relativeexpression of IRF7 in limited SSc (lSSc) and diffuse SSc (dSSc) was significantly increased compared with healthy subjects (p< 0.05). The relative expression of STAT1 transcripts in PBMCs was not statistically significantly different between the patientgroup and the control group. The correlation between IRF7 expression and the Rodnan score (RS) of the disease was significant.Considering the overexpression of IRF7 in SSc patients and significant correlation between the IRF7 and the Rodnan score ofthe disease, it is suggested that impaired expression of IRF7 is involved in the pathogenesis of SSc.
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