Dietary oxidized fatty acids may enhance intestinal apolipoprotein A-I production

被引:0
|
作者
Rong, R
Ramachandran, S
Penumetcha, M
Khan, N
Parthasarathy, S [1 ]
机构
[1] Emory Univ, Sch Med, Dept Gynecol & Obstet, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Nutr & Hlth Sci Program, Atlanta, GA 30322 USA
关键词
atherosclerosis; oxidized linoleic acid; Caco-2; cells; high density lipoprotein; oxidative stress; brush border; 13-HPODE; 13-HODE; antioxidant defense; oxidized low density lipoprotein; apolipoprotein B; PPAR-gamma;
D O I
暂无
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
Apolipoprotein (apo)A-I, the major protein component of HDL, is synthesized principally in the small intestine and liver. Recently we observed an increase in plasma apoA-I level in humans who were on an oxidized fat diet. To test whether oxidized fatty acids could affect apoA-I synthesis, we incubated day 4 (undifferentiated) and day 14 (differentiated) Caco-2 cells with varying concentrations of oxidized linoleic acid (ox-linoleic acid) (5, 10, and 25 muM) and unoxidized linoleic acid for 24 h. Ox-linoleic acid caused a dose-dependent increase in the levels of apoA-I protein in both differentiated and undifferentiated Caco-2 cells as assessed by ELISA and Western blot analysis. Whereas apoB production was not increased by ox-linoleic acid in both day 4 and day 14 Caco-2 cells. The mRNA expression for apoA-I paralleled the protein expression when measured by RTPCR. We also found that both day 4 and day 14 Caco-2 cells did express peroxisomal proliferator-activated receptor-gamma (PPAR-gamma). mRNA and PPAR-gamma ligand could increase apoA-I secretion in these cells. Therefore we propose that the mechanism for the induction of apoA-I might include PPAR-gamma for which oxidized fatty acid is a ligand.-Rong, R., S. Ramachandran, M. Penumetcha, N. Khan, and S. Parthasarathy. Dietary oxidized fatty acids may enhance intestinal apolipoprotein A-I production.
引用
收藏
页码:557 / 564
页数:8
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