Abstract
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 μM) 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 RT-PCR. We also found that both day 4 and day 14 Caco-2 cells did express peroxisomal proliferator-activated receptor-γ (PPAR-γ). mRNA and PPAR-γ ligand could increase apoA-I secretion in these cells. Therefore we propose that the mechanism for the induction of apoA-I might include PPAR-γ for which oxidized fatty acid is a ligand.
Original language | English |
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Pages (from-to) | 557-564 |
Number of pages | 8 |
Journal | Journal of Lipid Research |
Volume | 43 |
Issue number | 4 |
Publication status | Published - 2002 |
Externally published | Yes |
Keywords
- 13-HODE
- 13-HPODE
- Antioxidant defense
- Apolipoprotein B
- Atherosclerosis
- Brush border
- Caco-2 cells
- High density lipoprotein
- Oxidative stress
- Oxidized linoleic acid
- Oxidized low density lipoprotein
- PPAR-γ