Lind Ulrika, Nilsson Tina, McPheat Jane, Strömstedt Per-Erik, Bamberg Krister, Balendran Clare, Kang Daiwu
Department of Molecular Pharmacology, AstraZeneca R&D Mölndal, Sweden.
Biochem Biophys Res Commun. 2005 Apr 29;330(1):233-41. doi: 10.1016/j.bbrc.2005.02.151.
Retinoic acid receptor-related orphan receptor-alpha (RORalpha) (NR1F1) is an orphan nuclear receptor with a potential role in metabolism. Previous studies have shown that RORalpha regulates transcription of the murine Apolipoprotein AI gene and human Apolipoprotein CIII genes. In the present study, we present evidence that RORalpha also induces transcription of the human Apolipoprotein AV gene, a recently identified apolipoprotein associated with triglyceride levels. Adenovirus-mediated overexpression of RORalpha increased the endogenous expression of ApoAV in HepG2 cells and RORalpha also enhanced the activity of an ApoAV promoter construct in transiently transfected HepG2 cells. Deletion and mutation studies identified three AGGTCA motifs in the ApoAV promoter that mediate RORalpha transactivation, one of which overlaps with a previously identified binding site for PPARalpha. Together, these results suggest a novel mechanism whereby RORalpha modulates lipid metabolism and implies RORalpha as a potential target for the treatment of dyslipidemia and atherosclerosis.
维甲酸受体相关孤儿受体α(RORα)(NR1F1)是一种孤儿核受体,在代谢中具有潜在作用。先前的研究表明,RORα调节小鼠载脂蛋白AI基因和人类载脂蛋白CIII基因的转录。在本研究中,我们提供证据表明,RORα还能诱导人类载脂蛋白AV基因的转录,该载脂蛋白是最近发现的与甘油三酯水平相关的载脂蛋白。腺病毒介导的RORα过表达增加了HepG2细胞中ApoAV的内源性表达,并且RORα还增强了瞬时转染的HepG2细胞中ApoAV启动子构建体的活性。缺失和突变研究在ApoAV启动子中鉴定出三个介导RORα反式激活的AGGTCA基序,其中一个与先前确定的PPARα结合位点重叠。总之,这些结果提示了一种RORα调节脂质代谢的新机制,并暗示RORα作为治疗血脂异常和动脉粥样硬化的潜在靶点。