LPS induces inflammatory responses in human aortic vascular smooth muscle cells via Toll-like receptor 4 expression and nitric oxide production

被引:83
作者
Heo, Sook-Kyoung [1 ,2 ]
Yun, Hyun-Jeong [1 ,2 ]
Noh, Eui-Kyu [3 ]
Park, Won-Hwan [1 ,2 ]
Park, Sun-Dong [1 ,2 ]
机构
[1] Dongguk Univ, Cardiovasc Med Res Ctr, Gyeongju City 780714, Gyeongbuk, South Korea
[2] Dongguk Univ, Dept Prescriptionol, Gyeongju City 780714, Gyeongbuk, South Korea
[3] Univ Ulsan, Coll Med, Ulsan Univ Hosp, Div Hematol Oncol, Ulsan 682714, South Korea
关键词
LPS; Anti-inflammation; TLR4; iNOS; NO;
D O I
10.1016/j.imlet.2008.07.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inflammation is an important event in the development of vascular diseases such as hypertension, atherosclerosis, and restenosis. In addition, the stimulation of Toll-like receptor 4 (TLR4) by lipopolysaccharide (LPS) induces the release of critical proinflammatory cytokines that activate potent immune responses. In this study, LPS was found to induce TLR4 expression and increased nitric oxide (NO) production by increasing the expression of inducible nitric oxide synthase (iNOS). Furthermore, LPS was found to induce interleukin (IL)-8 and vascular endothelial growth factor (VEGF) production, as well as intracellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) expression. Taken together, these results indicate that LPS induces inflammatory responses in HASMC. Moreover, NOS inhibitor (L-NAME) and anti-TLR4 mAb reduced the LPS-incluced NO, IL-8 and VEGF production and ICAM-1 expression. Additionally, TLR4 expression was reduced by NOS inhibitor. Taken together, these results indicate that LPS-incluced inflammatory responses are regulated by TLR4 expression and NO production. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 64
页数:8
相关论文
共 29 条
[1]  
Björkbacka H, 2006, CURR OPIN LIPIDOL, V17, P527
[2]   Atherosclerosis and inflammation: insights from rheumatoid arthritis [J].
Chung, Cecilia P. ;
Avalos, Ingrid ;
Raggi, Paolo ;
Stein, C. Michael .
CLINICAL RHEUMATOLOGY, 2007, 26 (08) :1228-1233
[3]  
Fan Jianglin, 2003, J Atheroscler Thromb, V10, P63
[4]   Mechanisms of disease: Toll-like receptors in cardiovascular disease [J].
Frantz, Stefan ;
Ertl, Georg ;
Bauersachs, Johann .
NATURE CLINICAL PRACTICE CARDIOVASCULAR MEDICINE, 2007, 4 (08) :444-454
[5]   Vascular adhesion molecules in atherosclerosis [J].
Galkina, Elena ;
Ley, Klaus .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (11) :2292-2301
[6]   LIGHT enhances the bactericidal activity of human monocytes and neutrophils via HVEM [J].
Heo, Sook-Kyoung ;
Ju, Seong-A ;
Lee, Sang-Chul ;
Park, Sang-Min ;
Choe, Suck-Young ;
Kwon, Byungsuk ;
Kwon, Byoung S. ;
Kim, Byung-Sam .
JOURNAL OF LEUKOCYTE BIOLOGY, 2006, 79 (02) :330-338
[7]   Monocyte chemoattractant protein-1 and coronary artery disease [J].
Ikeda, U ;
Matsui, K ;
Murakami, Y ;
Shimada, K .
CLINICAL CARDIOLOGY, 2002, 25 (04) :143-147
[8]   Interleukin-6 and acute coronary syndrome [J].
Ikeda, U ;
Ito, T ;
Shimada, K .
CLINICAL CARDIOLOGY, 2001, 24 (11) :701-704
[9]   Lipopolysaccharide regulates toll-like receptor 4 expression in human aortic smooth muscle cells [J].
Li, Hongli ;
He, Ying ;
Zhang, Jianjun ;
Sun, Shuhan ;
Sun, Baogui .
CELL BIOLOGY INTERNATIONAL, 2007, 31 (08) :831-835
[10]   Ginkgo biloba extract inhibits endotoxin-induced human aortic smooth muscle cell proliferation via suppression of toll-like receptor 4 expression and NADPH oxidase activation [J].
Lin, Feng-Yen ;
Chen, Yung-Hsiang ;
Chen, Yuh-Lien ;
Wu, Tao-Cheng ;
Li, Chi-Yuan ;
Chen, Jaw-Wen ;
Lin, Shing-Jong .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (05) :1977-1984