Hayashida Kazutaka, Kume Noriaki, Minami Manabu, Inui-Hayashida Atsuko, Mukai Eri, Toyohara Masako, Kita Toru
Department of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Japan.
Biochem Biophys Res Commun. 2004 Oct 22;323(3):1116-23. doi: 10.1016/j.bbrc.2004.08.193.
Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) is a receptor for oxidized LDL. Peroxisome proliferator-activated receptors (PPARs) are nuclear receptors regulating transcription of various genes. We examined effects of PPAR ligands on LOX-1 expression and their transcriptional regulation in vascular endothelial cells. PPARalpha-specific ligands, such as fenofibrate and WY-14643, but not PPARgamma-specific ligands induced LOX-1 expression. Reduced expression of PPARalpha by antisense oligonucleotides directed to PPARalpha blocked fenofibrate-induced LOX-1 expression. Luciferase reporter gene assays with deletion and point mutations in the LOX-1 promoter revealed that transcriptional activity of LOX-1 gene by fenofibrate was localized in the -114/-106 GC box. Electrophoretic mobility shift assays with the radiolabeled GC box sequence showed inducible bands by PPARalpha ligands, which is competitively suppressed by unlabeled GC box motif and by an antibody to PPARalpha. In conclusion, PPARalpha appears to be one of the key regulators that induce LOX-1 expression, utilizing the GC box as a promoter.
凝集素样氧化型低密度脂蛋白受体-1(LOX-1)是氧化型低密度脂蛋白的受体。过氧化物酶体增殖物激活受体(PPARs)是调节各种基因转录的核受体。我们研究了PPAR配体对血管内皮细胞中LOX-1表达及其转录调控的影响。PPARα特异性配体,如非诺贝特和WY-14643,但不是PPARγ特异性配体,可诱导LOX-1表达。用针对PPARα的反义寡核苷酸降低PPARα的表达可阻断非诺贝特诱导的LOX-1表达。对LOX-1启动子进行缺失和点突变的荧光素酶报告基因检测显示,非诺贝特对LOX-1基因的转录活性定位于-114/-106 GC盒。用放射性标记的GC盒序列进行电泳迁移率变动分析显示,PPARα配体可诱导条带,未标记的GC盒基序和PPARα抗体可竞争性抑制该条带。总之,PPARα似乎是利用GC盒作为启动子诱导LOX-1表达的关键调节因子之一。