Worgall T S, Sturley S L, Seo T, Osborne T F, Deckelbaum R J
Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.
J Biol Chem. 1998 Oct 2;273(40):25537-40. doi: 10.1074/jbc.273.40.25537.
Membrane physiology, plasma lipid levels, and intracellular sterol homeostasis are regulated by both fatty acids and cholesterol. Sterols regulate gene expression of key enzymes of cholesterol and fatty acid metabolism through proteolysis of the sterol regulatory element-binding protein (SREBP), which binds to sterol regulatory elements (SRE) contained in promoters of these genes. We investigated the effect of fatty acids on SRE-dependent gene expression and SREBP. Consistent results were obtained in three different cell lines (HepG2, Chinese hamster ovary, and CV-1) transfected with SRE-containing promoters linked to the luciferase expression vector. We show that micromolar concentrations of oleate and other polyunsaturated fatty acids (C18:2-C22:6) dose-dependently (0.075-0.6 mmol) decreased transcription of SRE-regulated genes by 20-75%. Few or no effects were seen with saturated free fatty acids. Fatty acid effects on SRE-dependent gene expression were independent and additive to those of exogenous sterols. Oleate decreased levels of the mature sterol regulatory element-binding proteins SREBP-1 and -2 and HMG-CoA synthase mRNA. Oleate had no effect in sterol regulation defective Chinese hamster ovary cells or in cells transfected with mutant SRE-containing promoters. We hypothesize that unsaturated fatty acids increase intracellular regulatory pools of cholesterol and thus affect mature SREBP levels and expression of SRE-dependent genes.
膜生理学、血浆脂质水平和细胞内固醇稳态受脂肪酸和胆固醇的共同调节。固醇通过固醇调节元件结合蛋白(SREBP)的蛋白水解作用来调节胆固醇和脂肪酸代谢关键酶的基因表达,SREBP可与这些基因启动子中所含的固醇调节元件(SRE)结合。我们研究了脂肪酸对SRE依赖性基因表达和SREBP的影响。在用与荧光素酶表达载体相连的含SRE启动子转染的三种不同细胞系(HepG2、中国仓鼠卵巢细胞和CV-1)中获得了一致的结果。我们发现,微摩尔浓度的油酸和其他多不饱和脂肪酸(C18:2 - C22:6)呈剂量依赖性(0.075 - 0.6 mmol)地使SRE调节基因的转录降低了20 - 75%。饱和游离脂肪酸几乎没有影响或没有影响。脂肪酸对SRE依赖性基因表达的影响与外源性固醇的影响无关且具有累加性。油酸降低了成熟的固醇调节元件结合蛋白SREBP-1和-2以及HMG-CoA合酶mRNA的水平。油酸对固醇调节缺陷的中国仓鼠卵巢细胞或用含突变SRE启动子转染的细胞没有影响。我们推测,不饱和脂肪酸增加了细胞内胆固醇的调节库,从而影响成熟SREBP水平和SRE依赖性基因的表达。