Obesity Research Centre, Institute for Molecular Bioscience, University of Queensland, Services Rd St. Lucia, Queensland, 4072 Australia.
J Steroid Biochem Mol Biol. 2012 Jul;130(3-5):159-68. doi: 10.1016/j.jsbmb.2011.06.009. Epub 2011 Jun 23.
Many nuclear hormone receptors (NRs) control lipid, glucose and energy homeostasis in an organ specific manner. Concordantly, dysfunctional NR signalling results in metabolic disease. The Retinoic acid receptor-related orphan receptor alpha (RORα), a member of the NR1F subgroup, is expressed in metabolic tissues. Previous studies identified the role of this NR in dyslipidemia, apo-lipoprotein metabolism and atherosclerosis. Recent data is underscoring the significant role of this orphan NR in the regulation of phase I/II metabolism (bile acids, xenobiotics, steroids etc.), adiposity, insulin signalling, and glucose tolerance. Moreover, oxygenated sterols, have been demonstrated to function as native ligands and inverse agonists. This review focuses on the rapidly emerging and evolving role of RORα in the control of lipid and glucose homeostasis in major mass metabolic tissues. Article from the special issue orphan receptors.
许多核激素受体 (NRs) 以器官特异性的方式控制脂质、葡萄糖和能量稳态。相应地,NR 信号传导功能障碍会导致代谢疾病。视黄酸受体相关孤儿受体 α (RORα) 是 NR1F 亚组的成员,在代谢组织中表达。先前的研究确定了该 NR 在血脂异常、载脂蛋白代谢和动脉粥样硬化中的作用。最近的数据强调了这种孤儿 NR 在调节 I/II 期代谢(胆汁酸、外源性物质、类固醇等)、肥胖、胰岛素信号和葡萄糖耐量方面的重要作用。此外,已经证明氧化甾醇可以作为天然配体和反向激动剂发挥作用。本综述重点介绍了 RORα 在主要代谢组织中控制脂质和葡萄糖稳态方面的快速出现和不断发展的作用。该文章来自于孤受体特刊。