Dysregulated NUB1 and Neddylation Enhances Rheumatoid Arthritis Fibroblast‐Like Synoviocyte Inflammatory Responses

接合作用 类风湿性关节炎 癌症研究 成纤维细胞 化学 医学 免疫学 泛素 基因 生物化学 泛素连接酶 体外
作者
Sho Sendo,Camilla Ribeiro Lima Machado,David L. Boyle,Robert J. Benschop,Narayanan B. Perumal,Eunice Choi,Wei Wang,Gary S. Firestein
出处
期刊:Arthritis & rheumatology [Wiley]
卷期号:76 (8): 1252-1262 被引量:12
标识
DOI:10.1002/art.42856
摘要

Objective Fibroblast‐like synoviocytes (FLS) contribute to the pathogenesis of rheumatoid arthritis (RA), in part due to activation of the proinflammatory transcription factor NF‐κB. Neddylation is modulated by the negative regulator of ubiquitin‐like protein (NUB) 1. We determined whether NUB1 and neddylation are aberrant in the models with RA FLS, thereby contributing to their aggressive phenotype. Methods Models with RA or osteoarthritis (OA) FLS were obtained from arthroplasty synovia. Real‐time quantitative polymerase chain reaction and Western blot analysis assessed gene and protein expression, respectively. NUB1 was overexpressed using an expression vector. NF‐κB activation was assessed by stimulating FLS with interleukin (IL)‐1β. Neddylation inhibitor (MLN4924) and proteasome inhibitor were used in migration and gene expression assays. MLN4924 was used in the model with K/BxN serum‐transfer arthritis. Results Enhanced H3K27ac and H3K27me3 peaks were observed in the NUB1 promoter in the OA FLS compared with the RA FLS. NUB1 was constitutively expressed by FLS, but induction by IL‐1β was significantly greater in the OA FLS. The ratio of neddylated cullin (CUL) 1 to nonneddylated CUL1 was lower in the OA FLS than the RA FLS. NUB1 overexpression decreased NF‐κB nuclear translocation and IL‐6 messenger RNA (mRNA) in IL‐1β–stimulated the RA FLS. MLN4924 decreased CUL1 neddylation, NF‐κB nuclear translocation, and IL‐6 mRNA in IL‐1β–stimulated the RA FLS. MLN4924 significantly decreased arthritis severity in the model with K/BxN serum‐transfer arthritis. Conclusion CUL1 neddylation and NUB1 induction is dysregulated in the models with RA, which increases FLS activation. Inhibition of neddylation is an effective therapy in an animal model of arthritis. These data suggest that the neddylation system contributes to the pathogenesis of RA and that regulation of neddylation could be a novel therapeutic approach. image
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
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
MashiroLin完成签到,获得积分10
刚刚
故里发布了新的文献求助10
1秒前
lhbuj发布了新的文献求助10
2秒前
qwer完成签到 ,获得积分10
2秒前
pin发布了新的文献求助10
3秒前
烟花的应助被qi采纳,获得10
3秒前
FashionBoy的应助被Yany采纳,获得10
4秒前
佰态完成签到 ,获得积分10
4秒前
Wells完成签到,获得积分10
5秒前
molihuakai的应助被Mole采纳,获得10
5秒前
6秒前
小张医生完成签到,获得积分10
6秒前
霜烬染完成签到,获得积分10
7秒前
思源的应助被石宇采纳,获得10
7秒前
金发光完成签到,获得积分10
8秒前
Mollymama完成签到 ,获得积分10
9秒前
9秒前
万能图书馆的应助被Liangang采纳,获得10
10秒前
马哈哈发布了新的文献求助10
10秒前
隐形曼青的应助被小小怪采纳,获得10
11秒前
11秒前
11秒前
12秒前
12秒前
酷波er的应助被niu采纳,获得10
13秒前
酷波er的应助被xuwen采纳,获得10
13秒前
14秒前
15秒前
Wxj246801发布了新的文献求助10
15秒前
陶瓷发布了新的文献求助10
16秒前
希望天下0贩的0的应助被林一采纳,获得10
16秒前
Yany发布了新的文献求助10
17秒前
斯文败类的应助被听话的采蓝采纳,获得10
17秒前
科研通AI2S的应助被星叶散客采纳,获得10
17秒前
天天快乐的应助被听话的采蓝采纳,获得10
17秒前
北化唯一真神完成签到 ,获得积分10
18秒前
18秒前
苏yb完成签到 ,获得积分10
19秒前
科研通AI6.2的应助被诸葛钢铁采纳,获得10
19秒前
19秒前
高分求助中
(应助此贴封号)通过应助OA文献获取积分 10000
Rosenblum, Global Change Biology 800
The Art of Interactive Teaching 600
Computational Chemical Reaction Engineering: Modeling, Simulation, and Design with MATLAB 600
Organizational Behavior 510
Management and the Arts 510
CLSI C56QG Examples of Hemolyzed, Icteric, and Lipemic/Turbid Samples Quick Guide 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 内科学 物理 有机化学 化学工程 生物化学 复合材料 光电子学 细胞生物学 心理学 量子力学 催化作用 物理化学 电极
热门帖子
关注 科研通微信公众号,转发送积分 7800868
求助须知:如何正确求助?哪些是违规求助? 9335550
关于积分的说明 20474529
捐赠科研通 7392525
什么是DOI,文献DOI怎么找? 3326479
关于科研通互助平台的介绍 2473394
邀请新用户注册赠送积分活动 2344317