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Quercetin increases macrophage cholesterol efflux to inhibit foam cell formation through activating PPARγ-ABCA1 pathway.

pmid: 26617799
pmc: PMC4637614
Quercetin increases macrophage cholesterol efflux to inhibit foam cell formation through activating PPARγ-ABCA1 pathway.
The accumulation of cholesterol in macrophages could induce the formation of foam cells and increase the risk of developing atherosclerosis. We wonder if quercetin, one of flavonoids with anti-inflammation functions in different cell types, could elevate the development of foam cells formation in atherosclerosis. We treated foam cells derived from oxLDL induced THP-1 cells with quercetin, and evaluated the foam cells formation, cholesterol content and apoptosis of the cells. We found that quercetin induced the expression of ABCA1 in differentiated THP-1 cells, and increased the cholesterol efflux from THP-1 cell derived foam cells. Eventually, cholesterol level and the formation of foam cell derived from THP-1 cells decreased after quercetin treatment. In addition, quercetin activated PPARγ-LXRα pathway to upregulate ABCA1 expression through increasing protein level of PPARγ and its transcriptional activity. Inhibition of PPARγ activity by siRNA knockdown or the addition of chemical inhibitor, GW9662, abolished quercetin induced ABCA1 expression and cholesterol efflux in THP-1 derived macrophages. Our data demonstrated that quercetin increased cholesterol efflux from macrophages through upregulating the expressions of PPARγ and ABCA1. Taken together, increasing uptake of quercetin or quercetin-rich foods would be an effective way to lower the risk of atherosclerosis.
- Second Affiliated Hospital of Zhengzhou University China (People's Republic of)
- Shanghai Institute of Nutrition and Health China (People's Republic of)
- Chinese Academy of Sciences China (People's Republic of)
- Shanghai Institutes for Biological Sciences China (People's Republic of)
- First Affiliated Hospital of Zhengzhou University China (People's Republic of)
Time Factors, Dose-Response Relationship, Drug, Apoptosis, Biological Transport, Orphan Nuclear Receptors, Transfection, Up-Regulation, Lipoproteins, LDL, PPAR gamma, Cholesterol, Cell Line, Tumor, Humans, Anilides, Quercetin, RNA Interference, ATP Binding Cassette Transporter 1, Foam Cells, Liver X Receptors, Signal Transduction
Time Factors, Dose-Response Relationship, Drug, Apoptosis, Biological Transport, Orphan Nuclear Receptors, Transfection, Up-Regulation, Lipoproteins, LDL, PPAR gamma, Cholesterol, Cell Line, Tumor, Humans, Anilides, Quercetin, RNA Interference, ATP Binding Cassette Transporter 1, Foam Cells, Liver X Receptors, Signal Transduction
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