Contrasting expression pattern of RNA-sensing receptors TLR7, RIG-I and MDA5 in interferon-positive and interferon-negative patients with primary Sjögren's syndrome

TLR7型 干扰素 免疫学 医学 MDA5型 受体 钻机-I 病毒学 Ⅰ型干扰素 小学(天文学) 生物 Toll样受体 先天免疫系统 核糖核酸 基因 内科学 RNA干扰 遗传学 天文 物理
作者
Naomi I. Maria,Eline C. Steenwijk,Arne IJpma,Cornelia G van Helden-Meeuwsen,Petra Vogelsang,Wouter Beumer,Zana Brkić,Paul Van Daele,P. Martin van Hagen,Peter J. van der Spek,Hemmo A. Drexhage,Marjan A. Versnel
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:76 (4): 721-730 被引量:71
标识
DOI:10.1136/annrheumdis-2016-209589
摘要

The interferon (IFN) type I signature is present in over half of patients with primary Sjögren's syndrome (pSS) and associated with higher disease-activity and autoantibody presence. Plasmacytoid dendritic cells (pDCs) are considered as the main source of enhanced IFN type I expression. The objective of this study was to unravel the molecular pathways underlying IFN type I bioactivity in pDCs of patients with pSS.Blood samples from 42 healthy controls (HC) and 115 patients with pSS were stratified according to their IFN type I signature. CD123+BDCA4+ pDCs and CD14+ monocytes were isolated from peripheral blood mononuclear cells (PBMCs). Genome-wide microarray analysis was conducted on sorted pDCs in a small sample set, followed by validation of differentially expressed genes of interest in pDCs and monocytes.We found an upregulation of endosomal toll-like receptor (TLR) 7, but not TLR9, in IFN-positive (IFNpos) pDCs (p<0.05) and monocytes (p=0.024). Additionally, the downstream signalling molecules MyD88, RSAD2 and IRF7 were upregulated, as were the cytoplasmic RNA-sensing receptors DDX58/retinoic acid inducible gene-I (RIG-I) and IFIH1/melanoma differentiation associated gene-5 (MDA5). In vitro triggering of the TLR7-pathway in HC PBMCs induced upregulation of DDX58/RIG-I and IFIH1/MDA5, and downregulated TLR9. The upregulation of TLR7, its downstream signalling pathway, DDX58/RIG-I and IFIH1/MDA5 were confined to patients with IFN-positive pSS. IFN-negative patients had a contrasting expression pattern-TLR7 normal, and decreased TLR9, RIG-I and MDA5.Here we conclude a contrasting expression pattern of the RNA-sensing receptors TLR7, RIG-I and MDA5 in pDCs and monocytes of patients with IFNpos pSS. This profile could explain the pathogenic IFN production and might reveal novel therapeutic targets in these patients.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
善良耳机完成签到,获得积分10
刚刚
小乐比完成签到,获得积分10
1秒前
伍六七完成签到,获得积分10
2秒前
甜甜圈完成签到 ,获得积分10
2秒前
淡定的健柏完成签到 ,获得积分10
3秒前
鳗鱼友灵完成签到,获得积分10
3秒前
大渣饼完成签到 ,获得积分10
3秒前
贪玩绿柳完成签到,获得积分10
4秒前
bkagyin应助YHX采纳,获得10
4秒前
4秒前
4秒前
中宝完成签到,获得积分10
4秒前
SYLH应助害怕的小伙采纳,获得30
4秒前
野鸽儿完成签到 ,获得积分10
6秒前
路易斯完成签到,获得积分10
6秒前
最好的完成签到,获得积分10
6秒前
上官若男应助如风随水采纳,获得10
7秒前
8秒前
8秒前
亮仔发布了新的文献求助10
8秒前
靖瑞丰发布了新的文献求助10
8秒前
xu完成签到,获得积分20
8秒前
qwer完成签到,获得积分10
8秒前
8秒前
小谢完成签到,获得积分10
9秒前
Nerozhang完成签到,获得积分10
10秒前
10秒前
jignjing完成签到,获得积分10
12秒前
美满的高丽完成签到,获得积分10
12秒前
12秒前
12秒前
锦城纯契完成签到 ,获得积分10
12秒前
Eric完成签到,获得积分10
12秒前
害羞的乌完成签到 ,获得积分10
13秒前
13秒前
小尘埃完成签到,获得积分10
13秒前
天天快乐应助氯化氟采纳,获得10
13秒前
ludong_0完成签到,获得积分10
14秒前
萝卜仔完成签到 ,获得积分10
14秒前
15秒前
高分求助中
The Mother of All Tableaux Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 2400
Ophthalmic Equipment Market by Devices(surgical: vitreorentinal,IOLs,OVDs,contact lens,RGP lens,backflush,diagnostic&monitoring:OCT,actorefractor,keratometer,tonometer,ophthalmoscpe,OVD), End User,Buying Criteria-Global Forecast to2029 2000
Optimal Transport: A Comprehensive Introduction to Modeling, Analysis, Simulation, Applications 800
Official Methods of Analysis of AOAC INTERNATIONAL 600
ACSM’s Guidelines for Exercise Testing and Prescription, 12th edition 588
Residual Stress Measurement by X-Ray Diffraction, 2003 Edition HS-784/2003 588
T/CIET 1202-2025 可吸收再生氧化纤维素止血材料 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3950076
求助须知:如何正确求助?哪些是违规求助? 3495418
关于积分的说明 11077056
捐赠科研通 3225984
什么是DOI,文献DOI怎么找? 1783357
邀请新用户注册赠送积分活动 867663
科研通“疑难数据库(出版商)”最低求助积分说明 800855