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不饱和脂肪酸通过肝X受体/视黄醇X受体反应元件抑制ATP结合盒转运体G1(ABCG1)和ABCA1基因的表达。

Unsaturated fatty acids suppress the expression of the ATP-binding cassette transporter G1 (ABCG1) and ABCA1 genes via an LXR/RXR responsive element.

作者信息

Uehara Yoshinari, Miura Shin-ichiro, von Eckardstein Arnold, Abe Satomi, Fujii Akihiro, Matsuo Yoshino, Rust Stephan, Lorkowski Stefan, Assmann Gerd, Yamada Tatsuo, Saku Keijiro

机构信息

Department of Neurology and Healthcare, Fukuoka University Hospital, 7-45-1 Nanakuma, Jonan-ku, 814-0180 Fukuoka, Japan.

出版信息

Atherosclerosis. 2007 Mar;191(1):11-21. doi: 10.1016/j.atherosclerosis.2006.04.018. Epub 2006 May 30.

Abstract

ATP-binding cassette transporters (ABC) G1 and ABCA1 are membrane cholesterol transporters and have been implicated to mediate cholesterol efflux from cells in the presence of high density lipoproteins and its major protein constituent apolipoprotein A-I, respectively. We previously demonstrated that unsaturated fatty acids suppress the stimulatory effects of oxysterols and retinoids on ABCA1 gene transcription. We here demonstrate that unsaturated fatty acids significantly suppress the stimulatory effects of oxysterols and retinoids on the expression of ABCG1 mRNA and protein and the activity of the wild-type human ABCG1 promoter as well as ABCA1. Mutation or deletion of the DR4 element within the ABCG1 or ABCA1 promoters, to which the transcriptional inducers LXR and RXR bind, abolished the suppressive effects of unsaturated fatty acids. Our observations provide the first evidence that unsaturated fatty acids suppress ABCG1 gene expression by a mechanism which involves the binding of LXR/RXR to the promoters. Suppression of both the ABCA1 and ABCG1 genes may indicate that unsaturated fatty acids suppress not only cholesterol efflux to apoA-I and thereby nascent HDL formation but also HDL-dependent cholesterol efflux from vascular cells.

摘要

ATP结合盒转运蛋白(ABC)G1和ABCA1是膜胆固醇转运蛋白,分别被认为在高密度脂蛋白及其主要蛋白质成分载脂蛋白A-I存在的情况下介导细胞内胆固醇流出。我们之前证明不饱和脂肪酸可抑制氧化甾醇和类视黄醇对ABCA1基因转录的刺激作用。我们在此证明,不饱和脂肪酸可显著抑制氧化甾醇和类视黄醇对ABCG1 mRNA和蛋白质表达、野生型人ABCG1启动子活性以及ABCA1的刺激作用。ABCG1或ABCA1启动子内转录诱导剂肝X受体(LXR)和视黄醇X受体(RXR)结合的DR4元件发生突变或缺失,消除了不饱和脂肪酸的抑制作用。我们的观察提供了首个证据,表明不饱和脂肪酸通过一种涉及LXR/RXR与启动子结合的机制抑制ABCG1基因表达。ABCA1和ABCG1基因均受到抑制,这可能表明不饱和脂肪酸不仅抑制胆固醇向载脂蛋白A-I的流出,从而抑制新生高密度脂蛋白的形成,还抑制血管细胞中高密度脂蛋白依赖性胆固醇流出。

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