| Literature DB >> 26772887 |
Duo Gong1, Hai-Peng Cheng1, Wei Xie1, Min Zhang1, Dan Liu1, Gang Lan1, Chong Huang1, Zhen-Wang Zhao1, Ling-Yan Chen1, Feng Yao1, Yu-Lin Tan1, Liang Li1, Xiao-Dan Xia1, Xi-Long Zheng2, Zong-Bao Wang3, Chao-Ke Tang4.
Abstract
This study was designed to evaluate whether CSE/H2S system, which is regulated by miR-216a, regulated ABCA1-mediated cholesterol efflux and cholesterol contents in THP-1 macrophages-derived foam cells. Our qPCR and western blotting results showed that CSE/H2S significantly up-regulated the expression of ATP-binding cassette transporter A1 (ABCA1) mRNA and protein via PI3K/AKT pathway in foam cells derived from human THP-1 macrophages. The miR-216a directly targeted 3' untranslated region of CSE. It significantly reduced CSE and ABCA1 expression, and also decreased the phosphorylation of PI3K and AKT. Additionally, cholesterol efflux decreased, and cholesterol levels increased in THP-1 macrophage-derived foam cells in response to treatment with miR-216a. Our study demonstrates that CSE/H2S system is regulated by miR-216a, and regulates ABCA1-mediated cholesterol efflux and cholesterol levels through the PI3K/AKT pathway.Entities:
Keywords: ABCA1; CSE; Cholesterol efflux; Endogenous H(2)S; PI3K/AKT pathway; miR-216a
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Year: 2016 PMID: 26772887 DOI: 10.1016/j.bbrc.2016.01.003
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575