Inhibition of glycogen synthase kinase-3β suppresses inflammatory responses in rheumatoid arthritis fibroblast-like synoviocytes and collagen-induced arthritis

被引:38
作者
Kwon, Yong-Jin [1 ]
Yoon, Chong-Hyeon [2 ]
Lee, Sang-Won [1 ]
Park, Yong-Beom [1 ]
Lee, Soo-Kon [1 ]
Park, Min-Chan [1 ]
机构
[1] Yonsei Univ, Coll Med, Dept Internal Med, Div Rheumatol, Seoul 135720, South Korea
[2] Catholic Univ Korea, Coll Med, Dept Internal Med, Div Rheumatol, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Rheumatoid arthritis; Glycogen synthase kinase-3 beta; Fibroblast-like synoviocytes; Collagen induced arthritis; FACTOR-KAPPA-B; ACTIVATED PROTEIN-KINASE; TUMOR-NECROSIS-FACTOR; N-TERMINAL KINASE; SYNOVIAL FIBROBLASTS; CYTOKINE PRODUCTION; GSK-3; INHIBITORS; CELL-SURVIVAL; GLYCOGEN-SYNTHASE-KINASE-3-BETA; PHOSPHORYLATION;
D O I
10.1016/j.jbspin.2013.09.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Glycogen synthase kinase (GSK)-3 beta, a serine/threonine protein kinase, has been implicated as a regulator of the inflammatory response. This study was performed to evaluate the effect of selective GSK-3 beta inhibitors in rheumatoid arthritis (RA) fibroblast-like synoviocytes (FLS) and collagen-induced arthritis (CIA). Method: FLS from RA patients were treated with selective GSK-3 beta inhibitors, including lithium chloride, 6-bromoindirubin-3'-oxime (BIO), or 4-benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione (TDZD-8). The effects of GSK-3 beta inhibition on pro-inflammatory mediators were determined by real-time PCR and ELISA. The levels of NF-kappa B, phosphorylated JNK, c-jun, ATF-2 and p-38 proteins were evaluated by western blot analysis. The in vivo effects of GSK-3 beta inhibitors were examined in mice with CIA. Results: Treatment of RA FLS with GSK-3 beta inhibitors induced dose-dependent reductions in gene expression and the production of pro-inflammatory mediators. The levels of NF-kappa B, phosphorylated JNK, c-jun, ATF-2 and p-38 were decreased following treatment with GSK-3 beta inhibitors. GSK-3 beta inhibitors treatment attenuated clinical and histological severities of CIA in mice. Infiltration of T-cells, macrophages, and tartrate-resistant acid phosphatase positive cells was decreased in joint sections of CIA mice by GSK-3 beta inhibitors treatment. Serum levels of IL-1 beta, IL-6, TNF-alpha. and IFN-gamma in CIA mice were also significantly decreased in dose-dependent manners by treatment with GSK-3 beta inhibitors. Conclusion: Treatment with GSK-3 beta inhibitors suppressed inflammatory responses in RA FLS and CIA mice. These findings suggest that the inhibition of GSK-3 beta can be used as an effective therapeutic agent for RA. (C) 2013 Societe francaise de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:240 / 246
页数:7
相关论文
共 40 条
[1]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[2]   GSK3β Negatively Regulates Oligodendrocyte Differentiation and Myelination In Vivo [J].
Azim, Kasum ;
Butt, Arthur M. .
GLIA, 2011, 59 (04) :540-553
[3]   Inhibition of glycogen synthase kinase-3β prevents NSAID-induced acute kidney injury [J].
Bao, Hao ;
Ge, Yan ;
Zhuang, Shougang ;
Dworkin, Lance D. ;
Liu, Zhihong ;
Gong, Rujun .
KIDNEY INTERNATIONAL, 2012, 81 (07) :662-673
[4]   Glycogen synthase kinase-3β inhibition attenuates asthma in mice [J].
Bao, Zhang ;
Lim, Shuhui ;
Liao, Wupeng ;
Lin, Yuzhi ;
Thiemermann, Christoph ;
Leung, Bernard P. ;
Wong, W. S. Fred .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 176 (05) :431-438
[5]   Cell and cytokine imbalances in rheumatoid synovitis [J].
Boissier, Marie-Christophe .
JOINT BONE SPINE, 2011, 78 (03) :230-234
[6]   Phosphorylation of serine 468 by GSK-3β negatively regulates basal p65 NF-κB activity [J].
Buss, H ;
Dörrie, A ;
Schmitz, ML ;
Frank, R ;
Livingstone, M ;
Resch, K ;
Kracht, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (48) :49571-49574
[7]   Inhibition of glycogen synthase kinase-3β attenuates the development of carrageenan-induced lung injury in mice [J].
Cuzzocrea, S. ;
Crisafulli, C. ;
Mazzon, E. ;
Esposito, E. ;
Muia, C. ;
Abdelrahman, M. ;
Di Paola, R. ;
Thiemermann, C. .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 149 (06) :687-702
[8]   Glycogen synthase kinase 3β inhibition reduces the development of nonseptic shock induced by zymosan in mice [J].
Cuzzocrea, Salvatore ;
Di Paola, Rosanna ;
Mazzon, Emanuela ;
Crisafulli, Concetta ;
Genovese, Tiziana ;
Muia, Carmelo ;
Abdelrahman, Maha ;
Esposito, Emanuela ;
Thiemermann, Christoph .
SHOCK, 2007, 27 (01) :97-107
[9]   Glycogen synthase kinase-3β inhibition attenuates the degree of arthritis caused by type II collagen in the mouse [J].
Cuzzocrea, Salvatore ;
Mazzon, Emanuela ;
Di Paola, Rosanna ;
Muia, Carmelo ;
Crisafulli, Concetta ;
Dugo, Laura ;
Collin, Marika ;
Britti, Domenico ;
Caputi, Achille P. ;
Thiemermann, Christoph .
CLINICAL IMMUNOLOGY, 2006, 120 (01) :57-67
[10]   JNK1 modulates osteoclastogenesis through both c-Jun phosphorylation-dependent and -independent mechanisms [J].
David, JP ;
Sabapathy, K ;
Hoffmann, O ;
Idarraga, MH ;
Wagner, EF .
JOURNAL OF CELL SCIENCE, 2002, 115 (22) :4317-4325