Gold nanoparticles attenuate LPS-induced NO production through the inhibition of NF-κB and IFN-β/STAT1 pathways in RAW264.7 cells

被引:93
作者
Ma, Ji Su [1 ,2 ]
Kim, Wan Jae [1 ,2 ]
Kim, Jae Jin [1 ,2 ]
Kim, Tack Joong [3 ]
Ye, Sang Kyu [4 ]
Song, Min Dong [1 ,2 ]
Kang, Hyun [1 ,2 ]
Kim, Dong Woo [5 ]
Moon, Won Kook [5 ]
Lee, Kwang Ho [1 ,2 ]
机构
[1] Konkuk Univ, Biofood & Drug Res Ctr, Coll Biomed & Hlth Sci, Chungju 380701, South Korea
[2] Konkuk Univ, Dept Biotechnol, Coll Biomed & Hlth Sci, Chungju 380701, South Korea
[3] Yonsei Univ, Inst Biomat, Div Biol Sci & Technol, Wonju 220710, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Pharmacol, Seoul 110799, South Korea
[5] Nat F&P Co, Seoul 138200, South Korea
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2010年 / 23卷 / 03期
关键词
Gold nanoparticles; Lipopolysaccharide (LPS); Signal transducer and activator of transcription 1 (STAT1); Nitric oxide (NO); Inducible nitric synthase (iNOS); Interferon-beta (IFN-beta); NITRIC-OXIDE SYNTHASE; GENE-EXPRESSION; MOUSE MACROPHAGES; ACTIVATION; INDUCTION; KINASE; BETA; BIOCOMPATIBILITY; RECOGNITION; APOPTOSIS;
D O I
10.1016/j.niox.2010.06.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macrophage-derived nitric oxide (NO) plays an important role in protection against microbial infection in immune responses. Overproduction of NO by inducible nitric synthase (iNOS) is known to be closely correlated with the pathology of a variety of diseases and inflammations. In this study, we investigated the inhibitory effect of polyethylene glycol coated gold nanoparticles (GNP) on NO production and its molecular mechanism in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. It was found that GNP inhibited LPS-induced NO production and iNOS expression in RAW264.7 cells. Furthermore, GNP suppressed LPS-induced activation of NF-kappa B through the inhibition of Akt activity. GNP also inhibited LPS-induced phosphorylation of signal transducer and activator of transcription 1 (STAT1) via down-regulation of interferon-beta (IFN-beta) expression. Our results suggest that GNP inhibits NO production and iNOS expression through blocking the activation of NF-kappa B and STAT1 in LPS-stimulated RAW264.7 cells. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:214 / 219
页数:6
相关论文
共 41 条
[11]   Nanobiotechnology: the promise and reality of new approaches to molecular recognition [J].
Fortina, P ;
Kricka, LJ ;
Surrey, S ;
Grodzinski, P .
TRENDS IN BIOTECHNOLOGY, 2005, 23 (04) :168-173
[12]  
Gao JJ, 1998, J IMMUNOL, V161, P4803
[13]   NF-κB and rel proteins:: Evolutionarily conserved mediators of immune responses [J].
Ghosh, S ;
May, MJ ;
Kopp, EB .
ANNUAL REVIEW OF IMMUNOLOGY, 1998, 16 :225-260
[14]   Both p38αMAPK and JNK/SAPK pathways are important for induction of nitric-oxide synthase by interleukin-1β in rat glomerular mesangial cells [J].
Guan, ZH ;
Buckman, SY ;
Springer, LD ;
Morrison, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (51) :36200-36206
[15]   LPS induction of gene expression in human monocytes [J].
Guha, M ;
Mackman, N .
CELLULAR SIGNALLING, 2001, 13 (02) :85-94
[16]   Lipopolysaccharide activates Akt in vascular smooth muscle cells resulting in induction of inducible nitric oxide synthase through nuclear factor-kappa B activation [J].
Hattori, Y ;
Hattori, S ;
Kasai, K .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2003, 481 (2-3) :153-158
[17]   Inhibition of nitric oxide synthase as a potential therapeutic target [J].
Hobbs, AJ ;
Higgs, A ;
Moncada, S .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1999, 39 :191-220
[18]   Biocompatibility of poly(ether)urethane-gold nanocomposites [J].
Hsu, Shan-Hui ;
Tang, Cheng-Ming ;
Tseng, Hsiang-Jung .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2006, 79A (04) :759-770
[19]  
Jeon YJ, 2000, J PHARMACOL EXP THER, V294, P548
[20]   Eleutherococcus senticosus extract attenuates LPS-induced NOS expression through the inhibition of Akt and JNK pathways in murine macrophage [J].
Jung, Chang Hwa ;
Jung, Hee ;
Shin, Yong-Cheol ;
Park, Jong-Hyeong ;
Jun, Chan-Yong ;
Kim, Hyung-Min ;
Yim, Hee-Sun ;
Shin, Min-Gyu ;
Bae, Hyun-Soo ;
Kim, Sung-Hoon ;
Ko, Seong-Gyu .
JOURNAL OF ETHNOPHARMACOLOGY, 2007, 113 (01) :183-187