Fair A, Pritchard K A
Department of Experimental Pathology, New York Medical College, Valhalla 10595.
Biochem Biophys Res Commun. 1994 Jun 15;201(2):1014-20. doi: 10.1006/bbrc.1994.1803.
This study examines the effects of oxidized low density lipoprotein (ox-LDL) on mononuclear cell arachidonic acid (AA) metabolism. U937 and HL60 cells, employed as models for mononuclear cells and promyelocytic cells, respectively, were exposed to ox-LDL (20 micrograms protein/ml) for 24 hours. HPLC analysis of 1-14C-AA metabolites indicates that ox-LDL increases U937 and HL60 cell production of 15-hydroxyeicosatetraenoic acid (15-HETE) and 5-hydroxyeicosatetraenoic acid (5-HETE). Northern analysis indicates that ox-LDL increases U937 cell FLAP transcript levels 10-times control levels but did not appear to alter 5-lipoxygenase (5-LO) mRNA levels. In contrast, ox-LDL increases HL60 cell transcript levels for FLAP and 5-LO 1.5 times and 10 times control levels, respectively. Thus, we propose that ox-LDL plays an important role in the up-regulation of the 5-LO pathway in mononuclear cells. Such activation may explain, in part, the mechanisms by which ox-LDL promotes atherogenesis.
本研究检测氧化型低密度脂蛋白(ox-LDL)对单核细胞花生四烯酸(AA)代谢的影响。分别以U937细胞和HL60细胞作为单核细胞和早幼粒细胞的模型,将其暴露于ox-LDL(20微克蛋白/毫升)中24小时。对1-14C-AA代谢产物进行高效液相色谱分析表明,ox-LDL可增加U937细胞和HL60细胞中15-羟基二十碳四烯酸(15-HETE)和5-羟基二十碳四烯酸(5-HETE)的生成。Northern印迹分析表明,ox-LDL可使U937细胞中5-脂氧合酶激活蛋白(FLAP)转录水平增加至对照水平的10倍,但似乎并未改变5-脂氧合酶(5-LO)的mRNA水平。相比之下,ox-LDL可使HL60细胞中FLAP和5-LO的转录水平分别增加至对照水平的1.5倍和10倍。因此,我们认为ox-LDL在单核细胞中5-LO途径的上调中起重要作用。这种激活可能部分解释了ox-LDL促进动脉粥样硬化形成的机制。