ABCA1
流出
胆固醇
THP1细胞系
胆固醇逆向转运
化学
细胞生物学
小RNA
载脂蛋白A1
下调和上调
载脂蛋白B
分子生物学
生物
脂蛋白
生物化学
细胞培养
运输机
基因
遗传学
作者
Xiao-Er Tang,Heng Li,Lingyan Chen,Xiao-Dan Xia,Zhen-Wang Zhao,Xi‐Long Zheng,Guo-Jun Zhao,Chao‐Ke Tang
出处
期刊:Cytokine
[Elsevier BV]
日期:2018-04-24
卷期号:122: 154385-154385
被引量:25
标识
DOI:10.1016/j.cyto.2018.04.028
摘要
Previous studies suggest that IL-8 has an important role in the regulation of cholesterol efflux, but whether miRNAs are involved in this process is still unknown. The purpose of this study is to explore whether IL-8 promotes cholesterol accumulation by enhancing miR-183 expression in macrophages and its underlying mechanism. Treatment of THP-1 macrophage-derived foam cells with IL-8 decreased ABCA1 expression and cholesterol efflux. Using bioinformatics analyses and dual-luciferase reporter assays, we found that miR-183 was highly conserved during evolution and directly inhibited ABCA1 protein and mRNA expression by targeting ABCA1 3′UTR. MiR-183 directly regulated endogenous ABCA1 expression levels. Furthermore, IL-8 enhanced the expression of miR-183 and decrease ABCA1 expression. Cholesterol transport assays confirmed that IL-8 dramatically inhibited apolipoprotein AI-mediated ABCA1-dependent cholesterol efflux by increasing miR-183 expression. In contrast, treatment with anti-IL-8 antibody reversed these effects. IL-8 enhances the expression of miR-183, which then inhibits ABCA1 expression and cholesterol efflux. Our studies suggest that the IL-8-miR-183-ABCA1 axis may play an intermediary role in the development of atherosclerosis.
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