Unsaturated fatty acids selectively induce an inflammatory environment in human endothelial cells
Open Access
- 1 January 2002
- journal article
- research article
- Published by Elsevier in The American Journal of Clinical Nutrition
- Vol. 75 (1) , 119-125
- https://doi.org/10.1093/ajcn/75.1.119
Abstract
Background: Activation of the vascular endothelium by dietary fatty acids may be among the most critical early events in the development of atherosclerosis. However, the specific effects of fatty acids on inflammatory responses in endothelial cells are not fully understood. Objective: The present study focused on the induction of inflammatory genes in human endothelial cells exposed to individual dietary fatty acids. Because of the significance of nuclear factor κB (NF-κB) and activator protein 1 (AP-1) in the regulation of inflammatory gene expression, we also determined the effects of fatty acids on NF-κB and AP-1 transcriptional activation. Design: Human umbilical vein endothelial cells were exposed to dietary mono- and polyunsaturated 18-carbon fatty acids. Transcriptional activation of NF-κB and AP-1 was determined in human umbilical vein endothelial cells transfected with reporter constructs regulated by these transcription factors. Induction of the inflammatory genes was studied by use of reverse transcriptase–polymerase chain reaction. Results: Of the fatty acids studied, linoleic acid stimulated NF-κB and AP-1 transcriptional activation the most. In addition, treatment with this fatty acid markedly enhanced messenger RNA levels of tumor necrosis factor α, monocyte chemoattractant protein 1, vascular cell adhesion molecule 1, and intercellular adhesion molecule 1. Treatment with linolenic acid stimulated only a moderate induction of the genes encoding for these inflammatory mediators, and exposure to oleic acid either had no effect or resulted in decreased inflammatory gene messenger RNA. In addition, exposure to both linoleic and linolenic acids strongly stimulated induction of the phospholipid hydroperoxide glutathione peroxidase gene. Conclusion: Specific unsaturated dietary fatty acids, particularly linoleic acid, can selectively stimulate the development of a proinflammatory environment within the vascular endothelium.Keywords
This publication has 42 references indexed in Scilit:
- The Role of Methyl-Linoleic Acid Epoxide and Diol Metabolites in the Amplified Toxicity of Linoleic Acid and Polychlorinated Biphenyls to Vascular Endothelial CellsToxicology and Applied Pharmacology, 2001
- Oleic Acid Inhibits Endothelial ActivationArteriosclerosis, Thrombosis, and Vascular Biology, 1999
- 13‐HPODE and 13‐HODE modulate cytokine‐induced expression of endothelial cell adhesion molecules differentlyBioFactors, 1999
- Study of Gene Regulation by NF-κB and AP-1 in Response to Reactive Oxygen IntermediatesMethods, 1997
- Effects of oleate-rich and linoleate-rich diets on the susceptibility of low density lipoprotein to oxidative modification in mildly hypercholesterolemic subjects.Journal of Clinical Investigation, 1993
- Suppression of endotoxin mitogenicity of spleen cells by lipoxygenase inhibitors and its reversal by 13-hydroxyoctadecadienoic acidFEMS Immunology & Medical Microbiology, 1993
- Disruption of endothelial barrier function by lipolytic remnants of triglyceride-rich lipoproteinsAtherosclerosis, 1992
- Mechanisms of Cellular Uptake of Free Fatty AcidsAnnual Review of Nutrition, 1989
- Monocyte chemotactic protein gene expression by cytokine-treated human fibroblasts and endothelial cellsBiochemical and Biophysical Research Communications, 1989
- Atherogenesis: a postprandial phenomenon.Circulation, 1979