| Literature DB >> 26261553 |
Yan-Hua Sha1, Yan-Wei Hu1, Ji-Juan Gao1, Yan-Chao Wang1, Xin Ma2, Yu-Rong Qiu1, Shu-Fen Li1, Jia-Yi Zhao1, Chuan Huang1, Jing-Jing Zhao1, Jing-Bo Lu3, Chun-Min Kang1, Lei Zheng1, Qian Wang1.
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.Entities:
Keywords: ABCA1; LXA4; LXRα; THP-1 macrophage-derived foam cells; cholesterol efflux
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Year: 2015 PMID: 26261553 PMCID: PMC4525887
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625