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高密度脂蛋白(HDL)基因的调控:转录、转录后及翻译后调控。

Regulation of HDL genes: transcriptional, posttranscriptional, and posttranslational.

作者信息

Kardassis Dimitris, Gafencu Anca, Zannis Vassilis I, Davalos Alberto

机构信息

Department of Biochemistry, University of Crete Medical School and Institute of Molecular Biology and Biotechnology, Foundation of Research and Technology of Hellas, Heraklion, Crete, 71110, Greece,

出版信息

Handb Exp Pharmacol. 2015;224:113-79. doi: 10.1007/978-3-319-09665-0_3.

DOI:10.1007/978-3-319-09665-0_3
PMID:25522987
Abstract

HDL regulation is exerted at multiple levels including regulation at the level of transcription initiation by transcription factors and signal transduction cascades; regulation at the posttranscriptional level by microRNAs and other noncoding RNAs which bind to the coding or noncoding regions of HDL genes regulating mRNA stability and translation; as well as regulation at the posttranslational level by protein modifications, intracellular trafficking, and degradation. The above mechanisms have drastic effects on several HDL-mediated processes including HDL biogenesis, remodeling, cholesterol efflux and uptake, as well as atheroprotective functions on the cells of the arterial wall. The emphasis is on mechanisms that operate in physiologically relevant tissues such as the liver (which accounts for 80% of the total HDL-C levels in the plasma), the macrophages, the adrenals, and the endothelium. Transcription factors that have a significant impact on HDL regulation such as hormone nuclear receptors and hepatocyte nuclear factors are extensively discussed both in terms of gene promoter recognition and regulation but also in terms of their impact on plasma HDL levels as was revealed by knockout studies. Understanding the different modes of regulation of this complex lipoprotein may provide useful insights for the development of novel HDL-raising therapies that could be used to fight against atherosclerosis which is the underlying cause of coronary heart disease.

摘要

高密度脂蛋白(HDL)的调控作用在多个层面发挥,包括转录因子和信号转导级联反应在转录起始水平的调控;微小RNA和其他非编码RNA在转录后水平的调控,这些RNA与HDL基因的编码或非编码区域结合,调节mRNA的稳定性和翻译;以及蛋白质修饰、细胞内运输和降解在翻译后水平的调控。上述机制对多个HDL介导的过程具有显著影响,包括HDL的生物合成、重塑、胆固醇流出和摄取,以及对动脉壁细胞的抗动脉粥样硬化功能。重点关注在生理相关组织中起作用的机制,如肝脏(占血浆中总HDL-C水平的80%)、巨噬细胞、肾上腺和内皮细胞。对HDL调控有重大影响的转录因子,如激素核受体和肝细胞核因子,不仅在基因启动子识别和调控方面,而且在基因敲除研究揭示的对血浆HDL水平的影响方面都进行了广泛讨论。了解这种复杂脂蛋白的不同调控模式,可能为开发新型升高HDL的疗法提供有益的见解,这些疗法可用于对抗作为冠心病根本原因的动脉粥样硬化。

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