Linoleic acid induces MCP-1 gene expression in human microvascular endothelial cells through an oxidative mechanism

被引:21
|
作者
Lee, YW
Park, HJ
Hennig, B
Toborek, M
机构
[1] Univ Kentucky, Med Ctr, Dept Surg, Div Neurosurg, Lexington, KY 40536 USA
[2] Univ Kentucky, Dept Anim Sci, Lexington, KY 40546 USA
关键词
dietary fatty acids; vascular endothelium; cancer metastasis; atherosclerosis; oxidative stress;
D O I
10.1016/S0955-2863(01)00186-3
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
Linoleic acid is a dietary fatty acid that appears to play an important role in activation of the vascular endothelium. under a variety of pathological conditions, including development of atherosclerosis or cancer metastasis. Evidence indicates that inflammatory responses may be an underlying cause of endothelial cell pathology induced by linoleic acid. However, the profile of inflammatory mediators and the potential mechanisms involved in inflammatory reactions stimulated by the exposure to linoleic acid are not fully understood. The present study focused on the mechanisms of linoleic acid-induced expression of monocyte chemoattractant protein-1 (MCP-1) gene in human microvascular endothelial cells (EMEC-1). Treatment of HMEC-1 with increasing doses of linoleic acid markedly activated an oxidative stress-responsive transcription factor, nuclear factor-kappaB (NTF-kappaB). In addition, exposure to linoleic acid induced a time- and concentration-dependent overexpression of the MCP-1 gene. Increased MCP-1 mRNA levels were observed in HMEC-1 treated with linoleic acid at doses as, low as 10 muM. Linoleic acid-induced overexpression of the MCP-l gene was associated with a significant elevation of MCP-1 protein levels. Most importantly, preexposure of HMEC-1 to antioxidants, such as pyrrolidine dithiocarbamate (PDTC) or N-acetylcysteine (NAC), attenuated linoleic acid-induced MCP-1 mRNA expression. The obtained results indicate that linoleic acid triggers MCP-1 gene expression in human microvascular endothelial cells through oxidative stress/redox-related mechanisms. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:648 / 654
页数:7
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