首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Modified low density lipoproteins suppress production of a platelet-derived growth factor-like protein by cultured endothelial cells.
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Modified low density lipoproteins suppress production of a platelet-derived growth factor-like protein by cultured endothelial cells.

机译:修饰的低密度脂蛋白抑制培养的内皮细胞产生血小板源性生长因子样蛋白。

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摘要

Cultured endothelial cells (EC) produce a platelet-derived growth factor-like protein (PDGF-c) that stimulates the growth of cultured cells of mesenchymal origin. We have examined the effect of native plasma low density lipoprotein (LDL) and chemically modified LDL on production of PDGF-c by EC. Acetyl-LDL, but not native LDL, suppressed the production of PDGF-c by bovine aortic EC. Half-maximal inhibition was observed at a concentration of 25-75 micrograms of cholesterol per ml, and maximal inhibition (0-25% of control) at 150 micrograms of cholesterol per ml. EC treated with acetyl-LDL showed no morphological damage, there was no change in cell number, and the effect on production of PDGF-c was substantially reversed upon removal of the acetyl-LDL. The observed inhibition of PDGF-c production was specific, since total cellular and secreted protein synthesis were unaffected by acetyl-LDL. Acetyl-LDL suppressed PDGF-c production in both bovine aortic and human umbilical vein EC, but not in rat heart EC. This cell specificity correlated with the presence of scavenger receptors as measured by degradation of 125I-labeled acetyl-LDL and uptake of fluorescently labeled acetyl-LDL. Dimethylpropanediamine-LDL, a cationic modified lipoprotein, also inhibited PDGF-c production. The inhibition by both types of modified LDL was accompanied by significant intracellular cholesterol accumulation, suggesting a role for EC lipid composition in the regulation of production of PDGF-c.
机译:培养的内皮细胞(EC)产生血小板衍生的生长因子样蛋白(PDGF-c),该蛋白刺激间充质来源的培养细胞的生长。我们已经检查了天然血浆低密度脂蛋白(LDL)和化学修饰的LDL对EC生产PDGF-c的影响。乙酰基低密度脂蛋白(而非天然低密度脂蛋白)抑制牛主动脉EC产生PDGF-c。在每毫升25-75微克胆固醇的浓度下观察到最大抑制的一半,在每毫升150微克胆固醇下观察到最大抑制(对照的0-25%)。用乙酰基-LDL处理的EC没有表现出形态学损伤,细胞数没有变化,并且在去除乙酰基-LDL后,对PDGF-c产生的影响基本上被逆转了。观察到的对PDGF-c产生的抑制是特异性的,因为总细胞和分泌的蛋白质合成不受乙酰-LDL的影响。乙酰基低密度脂蛋白抑制牛主动脉和人脐静脉EC中PDGF-c的产生,但不抑制大鼠心脏EC中的PDGF-c的产生。该细胞特异性与清道夫受体的存在相关,如通过125 I标记的乙酰基-LDL的降解和荧光标记的乙酰基-LDL的摄取所测量的。阳离子修饰的脂蛋白二甲基丙二胺-LDL也抑制PDGF-c的产生。两种类型的修饰的LDL的抑制作用都伴随着大量的细胞内胆固醇蓄积,这表明EC脂质成分在调节PDGF-c的产生中起作用。

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