Antisense IRAK-1 oligonucleotide blocks activation of NF-κB and AP-1 induced by IL-18

被引:17
作者
Guo, FK [1 ]
Wu, SG [1 ]
机构
[1] First Mil Med Univ, Inst Pharmaceut Sci, Guangzhou 510515, Peoples R China
来源
IMMUNOPHARMACOLOGY | 2000年 / 49卷 / 03期
关键词
interleukin-18; interleukin-1 receptor-associated kinase-1 antisense oligonucleotide; nuclear factor-kappa B; activator protein-1;
D O I
10.1016/S0162-3109(00)00200-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin-18 (IL-18) is a novel proinflammatory cytokine. Most of the immune and inflammatory genes induced by IL-18 are nuclear factor-kappaB (NF-kappa B)- and activator protein-1 (AP-1)-regulated. Interleukin-1 receptor-associated kinase-1 (IRAK-1) has recently been shown to be involved in IL-18-stimulated activation of NF-kappa B and AP-1. The purpose of this study is to investigate the effects of preventing IRAK-1 expression by antisense IRAK-1 oligode oxynucleotide (ODN) on IL-18-stimulated activation of NF-kappa B and AP-1. Semiquantitative reverse transcription-PCR (RT-PCR) and western blot analysis revealed that antisense IRAK-1 ODN inhibited IRAK-1 mRNA and protein expression (P < 0.01). As a result, antisense IRAK-1 ODN attenuated IL-18-induced activation of NF-kappa B and AP-1 as measured by sandwich ELISA in a concentration (1-8 mu g ml(-1))- and time (5-24 h)-dependent fashion. These data suggest that antisense IRAK-1 ODN may share a role in the design of antiinflammatory therapeutics. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:241 / 246
页数:6
相关论文
共 16 条
[1]   The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[2]  
Barbera K, 1998, SEM HUM SCI, V12, P11
[3]   HYDROGEN-PEROXIDE MEDIATES AMYLOID-BETA PROTEIN TOXICITY [J].
BEHL, C ;
DAVIS, JB ;
LESLEY, R ;
SCHUBERT, D .
CELL, 1994, 77 (06) :817-827
[4]   ATHEROSCLEROSIS - BASIC MECHANISMS - OXIDATION, INFLAMMATION, AND GENETICS [J].
BERLINER, JA ;
NAVAB, M ;
FOGELMAN, AM ;
FRANK, JS ;
DEMER, LL ;
EDWARDS, PA ;
WATSON, AD ;
LUSIS, AJ .
CIRCULATION, 1995, 91 (09) :2488-2496
[5]   Overview of interleukin-18:: more than an interferon-γ inducing factor [J].
Dinarello, CA ;
Novick, D ;
Puren, AJ ;
Fantuzzi, G ;
Shapiro, L ;
Mühl, H ;
Yoon, DY ;
Reznikov, LL ;
Kim, SH ;
Rubinstein, M .
JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 63 (06) :658-664
[6]   IL-18:: A TH1-inducing, proinflammatory cytokine and new member of the IL-1 family [J].
Dinarello, CA .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1999, 103 (01) :11-24
[7]   Defective interleukin (IL)-18-mediated natural killer and T helper cell type 1 responses in IL-1 receptor-associated kinase (IRAK)-deficient mice [J].
Kanakaraj, P ;
Ngo, K ;
Wu, Y ;
Angulo, A ;
Ghazal, P ;
Harris, CA ;
Siekierka, JJ ;
Peterson, PA ;
Fung-Leung, WP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (07) :1129-1138
[8]  
Kashiwamura S, 1998, Nihon Rinsho, V56, P1798
[9]   Interleukin-18 activates the IRAK-TRAF6 pathway in mouse EL-4 cells [J].
Kojima, H ;
Takeuchi, M ;
Ohta, T ;
Nishida, Y ;
Arai, N ;
Ikeda, M ;
Ikegami, H ;
Kurimoto, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 244 (01) :183-186
[10]   Signal transduction pathways activated by the IL-1 receptor family: ancient signaling machinery in mammals, insects, and plants [J].
O'Neill, LAJ ;
Greene, C .
JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 63 (06) :650-657