Effects of fatty acids on endothelial cells: inflammation and monocyte adhesion

被引:36
作者
Grenon, S. Marlene [1 ,2 ,3 ]
Aguado-Zuniga, Jesus [2 ]
Hatton, Jason P. [2 ]
Owens, Christopher D. [3 ]
Conte, Michael S.
Hughes-Fulford, Millie [2 ,4 ]
机构
[1] Univ Calif San Francisco, Div Vasc & Endovasc Surg, San Francisco Surg Serv, Vet Affairs Med Ctr, San Francisco, CA 94121 USA
[2] Vet Affairs Med Ctr, Hughes Fulford Lab, San Francisco, CA 94121 USA
[3] Vet Affair Med Ctr, Dept Surg, San Francisco, CA USA
[4] Univ Calif San Francisco, Dept Med, San Francisco, CA 94121 USA
关键词
Endothelial cells; Monocytes; Polyunsaturated fatty acids; Inflammation; Adhesion molecules; NECROSIS-FACTOR-ALPHA; CARDIOVASCULAR-DISEASE; FISH-OIL; EICOSAPENTAENOIC ACID; DOCOSAHEXAENOIC ACID; MOLECULE EXPRESSION; ARTERY-DISEASE; KAPPA-B; OMEGA-3-FATTY-ACIDS; ATHEROSCLEROSIS;
D O I
10.1016/j.jss.2012.04.010
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Diet is known to have an important impact on cardiovascular health. n-3 Fatty acids (FAs), found in high quantity in fish oil, have demonstrated beneficial effects in patients with coronary artery disease. The role of n-6 FAs remains more controversial. The objective of this study was to examine the effect of arachidonic acid (AA), an n-6 FA, and eicosapentanoic acid (EPA), an n-3 FA, on the interaction between monocytes and endothelial cells (ECs). Design: We used a cellular model of ECs (EA.hy.926) and monocytes (human leukemic myelomonocytic U937). Confluent ECs were treated with AA or EPA, in the presence of tumor necrosis factor-alpha (TNF-alpha) or vehicle alone for either 4 or 24 h. Adhesion of monocytes to the endothelial monolayer was performed. For gene expression, reverse transcription, followed by real-time quantitative polymerase chain reaction, was performed. Results: There was a significant increase in adhesion of monocytes to the endothelial monolayer in the presence of n-6 FAs, both in the presence and in the absence of TNF-alpha at 4 and 24 h. The adhesion of monocytes to the endothelial monolayer was decreased with n-3 FAs at 24 h. Intercellular adhesion molecule 1, vascular cell adhesion molecule 1, E-Selectin, Interleukin 6, and TNF-alpha were significantly increased in ECs treated with n-6 FAs. Conclusions: We conclude that AA increases inflammation and enhances the ability of ECs to bind monocytes in vitro. EPA leads to a decrease in the ability of EA.hy.926 to bind monocytes, although the effect appears more modest. Taken together, these data indicate that the n-6 FA AA could potentiate inflammation and early events of atherosclerosis. Published by Elsevier Inc.
引用
收藏
页码:E35 / E43
页数:9
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