Effect of Docosahexaenoic Acid (DHA) on the Apoptosis of Human Endothelial ECV304 Cells.
- Author:
Young Youn KIM
1
;
Hyosook KIM
;
Mae Ha KIM
;
Soojeong JANG
;
Myoungsook LEE
Author Information
1. Division of Nutritional Medicine, Family Health and Welfare Center (FHWC), Seoul, Korea. mlee@sungshin.ac.kr
- Publication Type:Original Article
- Keywords:
DHA;
LA;
AA;
apoptosis;
human endothelial ECV304 cells;
caspase-3;
mitochondrial damage
- MeSH:
Apoptosis*;
Arachidonic Acid;
Atherosclerosis;
Caspase 3;
Cell Death;
Endothelial Cells;
Fatty Acids;
Fatty Acids, Unsaturated;
Humans*;
Linoleic Acid;
Lipid Peroxidation;
Risk Factors
- From:The Korean Journal of Nutrition
2006;39(4):357-365
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
DHA, one of w-3 fatty acids, modulates cell growth or death though the changes of apoptotic signaling in human endothelial ECV304 cells. We investigated the effects of DHA on the changes of apoptotic signaling in human vascular endothelial ECV304 cells using lipid peroxidation (LPO) metabolites. LPO could be originated by dietary polyunsaturated fatty acids such as linoleic acid (LA), arachidonic acid (AA) and docosahexaenoic acid (DHA). DHA caused cell death of ECV304 cells compared to LA, AA or control as evidenced by changes in cell morphology and MTT assay. LPO levels was significantly elevated by 10 fold in DHA-treated ECV 304 cells and caspase-3 activity was increased by DHA corresponding to increasing incubation times compared to control. One of reasons of the cell death in DHA-treated ECV304 cells could be expected that caspase activity, marker for mitochondrial damages, might be triggered by the increasing LPO levels. Our results strongly indicated that DHA induced LPO production has an important role on apoptotic signaling pathway in ECV304 cells. LPO production in endothelial cells which was metabolized by oxidation of dietary PUFA, might be one of risk factors in the initial progression of atherosclerosis.
