| Literature DB >> 31604677 |
Yanyong Xu1, Yang Xu1, Yingdong Zhu1, Huihui Sun1, Cody Juguilon1, Feng Li2, Daping Fan3, Liya Yin1, Yanqiao Zhang4.
Abstract
Macrophages play a crucial role in the pathogenesis of atherosclerosis, but the molecular mechanisms remain poorly understood. Here we show that microRNA-34a (miR-34a) is a key regulator of macrophage cholesterol efflux and reverse cholesterol transport by modulating ATP-binding cassette transporters ATP-binding cassette subfamily A member 1 (ABCA1) and ATP-binding cassette subfamily G member 1 (ABCG1). miR-34a also regulates M1 and M2 macrophage polarization via liver X receptor α. Furthermore, global loss of miR-34a reduces intestinal cholesterol or fat absorption by inhibiting cytochrome P450 enzymes CYP7A1 and sterol 12α-hydroxylase (CYP8B1). Consistent with these findings, macrophage-selective or global ablation of miR-34a markedly inhibits the development of atherosclerosis. Finally, therapeutic inhibition of miR-34a promotes atherosclerosis regression and reverses diet-induced metabolic disorders. Our studies outline a central role of miR-34a in regulating macrophage cholesterol efflux, inflammation, and atherosclerosis, suggesting that miR-34a is a promising target for treatment of cardiometabolic diseases.Entities:
Keywords: ABCA1; ABCG1; LXR; atherosclerosis; cholesterol efflux; inflammation; miR-34a
Mesh:
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Year: 2019 PMID: 31604677 PMCID: PMC6952168 DOI: 10.1016/j.ymthe.2019.09.008
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454