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根据疾病活动情况,调节炎症细胞因子产生的转录因子在白塞病患者外周血单个核细胞中的表达存在差异。

Transcription Factors Regulating Inflammatory Cytokine Production Are Differentially Expressed in Peripheral Blood Mononuclear Cells of Behçet Disease Depending on Disease Activity.

作者信息

Woo Min-Yeong, Yun Su Jin, Lee Mi Jin, Kim Kyongmin, Lee Eun-So, Park Sun

机构信息

Department of Microbiology, Ajou University School of Medicine, Suwon, Korea.; Department of Biomedical Sciences, The Graduate School, Ajou University, Suwon, Korea.

Department of Microbiology, Ajou University School of Medicine, Suwon, Korea.

出版信息

Ann Dermatol. 2017 Apr;29(2):173-179. doi: 10.5021/ad.2017.29.2.173. Epub 2017 Mar 24.

Abstract

BACKGROUND

Behçet disease (BD) is a relapsing inflammatory disease with increased production of inflammatory cytokines in peripheral blood mononuclear cells (PBMCs); however, the underlying molecular mechanisms are not well known.

OBJECTIVE

To analyze whether the differential expression of transcription factors is involved in the increased tumor necrosis factor (TNF)-α and interleukin (IL)-6 production by PBMCs of BD patients compared to healthy controls (HCs).

METHODS

Expression of transcription factors was examined by real-time reverse transcriptase-polymerase chain reaction and western blotting. Cytokine production by CD11b+ cells transfected with siRNAs against transcription factors was measured by enzyme-linked immunosorbent assay.

RESULTS

In the absence of lipopolysaccharide stimulation, the transcript level of CCAAT-enhancer-binding proteins (C/EBP) β was increased in PBMCs from patients with active BD compared to that in PBMCs from patients with stable BD. The C/EBPδ transcript level was higher in PBMCs from patients with active BD than in those from HCs. The activating transcription factor 3 (ATF3) transcript level was increased in PBMCs from patients with stable BD compared to that in PBMCs from HCs. siRNAs targeting C/EBPβ and C/EBPδ significantly reduced the production of IL-6 and TNF-α in lipopolysaccharide-stimulated CD11b+ cells from patients with BD as well as from HCs.

CONCLUSION

We found differential expression of C/EBPβ, C/EBPδ, and ATF3 in PBMCs from patients with BD depending on disease activity, indicating the involvement of these molecules in BD pathogenesis.

摘要

背景

白塞病(BD)是一种复发性炎症性疾病,外周血单核细胞(PBMCs)中炎性细胞因子的产生增加;然而,其潜在的分子机制尚不清楚。

目的

分析与健康对照(HCs)相比,转录因子的差异表达是否参与BD患者PBMCs中肿瘤坏死因子(TNF)-α和白细胞介素(IL)-6产生的增加。

方法

通过实时逆转录聚合酶链反应和蛋白质免疫印迹法检测转录因子的表达。用针对转录因子的小干扰RNA(siRNAs)转染CD11b+细胞后,通过酶联免疫吸附测定法测量细胞因子的产生。

结果

在无脂多糖刺激的情况下,与稳定期BD患者的PBMCs相比,活动期BD患者的PBMCs中CCAAT增强子结合蛋白(C/EBP)β的转录水平升高。活动期BD患者的PBMCs中C/EBPδ转录水平高于HCs的。与HCs的PBMCs相比,稳定期BD患者的PBMCs中激活转录因子3(ATF3)的转录水平升高。靶向C/EBPβ和C/EBPδ的siRNAs显著降低了来自BD患者以及HCs的脂多糖刺激的CD11b+细胞中IL-6和TNF-α的产生。

结论

我们发现BD患者的PBMCs中C/EBPβ、C/EBPδ和ATF3的表达因疾病活动状态而异,表明这些分子参与了BD的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9545/5383742/00a6a1c62657/ad-29-173-g001.jpg

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