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类风湿关节炎滑膜成纤维细胞中 ADP 核糖基化因子样蛋白 15 的功能特征。

Functional characterisation of ADP ribosylation factor-like protein 15 in rheumatoid arthritis synovial fibroblasts.

机构信息

Department of Genetics, University of Delhi South Campus, New Delhi, India.

Department of Rheumatology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Clin Exp Rheumatol. 2018 Jul-Aug;36(4):581-588. Epub 2018 Feb 14.

Abstract

OBJECTIVES

ARL15 is a novel susceptibility gene identified in a recent GWAS in a north Indian rheumatoid arthritis (RA) cohort. However, the role of ARL15 or ARF family genes in RA aetiology remains unknown. Therefore, we aimed to i) establish the expression of ARL15 in rheumatoid arthritis synovial fibroblasts (RASF) and ii) its functional characterisation by assessing its effects on major inflammatory cytokines and interacting partners using a knockdown approach.

METHODS

RASF were cultured from synovial tissue obtained from RA patients (n=5) and osteoarthritis (OA) patients (n=3) serving as controls. Expression of ARL15, ARF1 and ARF6 in RASF was checked by semi-quantitative PCR and western blots; and altered expression of ARL15, if any, by induction of RASF with TNF using real-time PCR. The effect of ARL15 on the expression of adiponectin, adiponectin receptor I, IL6 and GAPDH and on cell mobility by invasion and migration assays were assessed by siRNA mediated gene knockdown.

RESULTS

Expression of ARL15, ARF1 and ARF6 was confirmed in RASF and OASF samples but ARL15 expression remained unaltered on TNF induction. Notably, ARL15 knockdown resulted in downregulation of IL6 and GAPDH, upregulation of adiponectin and adiponectin receptor I genes; and significant reduction in migration and invasion of RASF. Genemania showed significant interactions of ARL15 with genes responsible for insulin resistance and phospholipase D.

CONCLUSIONS

This first report on ARL15 expression in RASF and its likely role in inflammation and metabolic syndromes through a TNF independent pathway, encourages hypothesis-free studies to identify additional pathways underlying RA disease biology.

摘要

目的

ARL15 是最近在印度北部类风湿关节炎 (RA) 队列的 GWAS 中发现的一个新的易感性基因。然而,ARL15 或 ARF 家族基因在 RA 发病机制中的作用仍不清楚。因此,我们旨在:i)确定 ARL15 在类风湿关节炎滑膜成纤维细胞 (RASF)中的表达;ii)通过使用敲低方法评估其对主要炎症细胞因子和相互作用伙伴的影响,对其功能进行特征分析。

方法

从 RA 患者(n=5)和骨关节炎 (OA) 患者(n=3)的滑膜组织中培养 RASF,作为对照。通过半定量 PCR 和 Western blot 检查 RASF 中 ARL15、ARF1 和 ARF6 的表达;并通过用 TNF 诱导 RASF 检查是否存在任何改变的 ARL15 表达,用实时 PCR 检测。通过 siRNA 介导的基因敲低,评估 ARL15 对脂联素、脂联素受体 I、IL6 和 GAPDH 的表达以及细胞迁移和侵袭能力的影响。

结果

在 RASF 和 OASF 样本中证实了 ARL15、ARF1 和 ARF6 的表达,但 TNF 诱导后 ARL15 表达不变。值得注意的是,ARL15 敲低导致 IL6 和 GAPDH 下调,脂联素和脂联素受体 I 基因上调;以及 RASF 的迁移和侵袭显著减少。Genemania 显示 ARL15 与负责胰岛素抵抗和磷脂酶 D 的基因有显著相互作用。

结论

这是首次报道 ARL15 在 RASF 中的表达及其通过 TNF 独立途径在炎症和代谢综合征中的可能作用,鼓励进行无假设研究,以确定 RA 疾病生物学的其他潜在途径。

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