Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8296125 | Biochemical and Biophysical Research Communications | 2017 | 18 Pages |
Abstract
miR-758-3p plays an important role via regulting ABCA1-mediated cholesterol efflux in atherosclerosis. However, the mechanism of miR-758-5p in cholesterol metabolism is still unclear. Here, we revealed that miR-758-5p decreased total cholesterol accumulation in THP-1 macrophage derived foam cells through markedly reducing cholesterol uptake, and no effect on the cholesterol efflux. Interestingly, computational analysis suggests that CD36 may be a target gene of miR-758-5p. Our study further demonstrated that miR-758-5p decreased CD36 expression at both protein and mRNA levels via targeting the CD36 3â²UTR in THP-1 macrophage derived foam cells. The present present study concluded that miR-758-5p decreases lipid accumulation of foam cell via regulating CD36-mediated the cholesterol uptake. Therefore, targeting miR-758-5p may offer a promising strategy to treat atherosclerotic vascular disease.
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Authors
Bi-Rong Li, Lin-Qin Xia, Jing Liu, Lin-Ling liao, Yang Zhang, Min Deng, Hui-Juan Zhong, Ting-Ting Feng, Ping-Ping He, Xin-Ping Ouyang,