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Lipoxin A4 promotes ABCA1 expression and cholesterol efflux through the LXRα signaling pathway in THP-1 macrophage-derived foam cells.
- Source :
-
International journal of clinical and experimental pathology [Int J Clin Exp Pathol] 2015 Jun 01; Vol. 8 (6), pp. 6708-15. Date of Electronic Publication: 2015 Jun 01 (Print Publication: 2015). - Publication Year :
- 2015
-
Abstract
- Adenosine triphosphate-binding cassette transporter A1 (ABCA1) is a crucial cholesterol transporter and plays a central role in the high density lipoproteins (HDL) cholesterol metabolism and lipid clearance from the foam cell. Lipoxin A4 (LXA4) is an endogenous lipid mediator that requires cell-cell interaction or cell-platelet interaction for its synthesis. The roles of LXA4 on inflammatory responses are well described, while its effects on mediating ABCA1 and underlying mechanisms remain unclear. In this study, we showed that LXA4 significantly increases expression of ABCA1 and LXRα in a dose-dependent manner in THP-1 macrophage-derived foam cells. Cellular cholesterol content was decreased while cholesterol efflux was increased by LXA4 treatment. However, after short interfering RNA of LXRα, the effects of LXA4 on ABCA1 expression and cholesterol metabolism were significantly abolished. These results provide evidence that LXA4 increases ABCA1 expression and promotes cholesterol efflux through LXRα pathway in THP-1 macrophage-derived foam cells.
- Subjects :
- Cell Line, Tumor
Dose-Response Relationship, Drug
Foam Cells metabolism
Humans
Liver X Receptors
Orphan Nuclear Receptors genetics
RNA Interference
Transfection
Up-Regulation
ATP Binding Cassette Transporter 1 metabolism
Cholesterol metabolism
Foam Cells drug effects
Lipoxins pharmacology
Orphan Nuclear Receptors metabolism
Signal Transduction drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1936-2625
- Volume :
- 8
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- International journal of clinical and experimental pathology
- Publication Type :
- Academic Journal
- Accession number :
- 26261553