期刊文献+

氧化型低密度脂蛋白促进巨噬细胞血凝素样氧化型低密度脂蛋白受体-1表达及辛伐他汀干预研究 被引量:2

Oxidized low density lipoprotein accelerates the expression of lectin fike oxidized low density lipoprotein receptor 1 of macrophages in rats and the effect of Simvanstatin intervention
原文传递
导出
摘要 目的:观察氧化型低密度脂蛋白(ox-LDL)对大鼠腹腔巨噬细胞血凝素样氧化型低密度脂蛋白受体-1(LOX-1)表达的影响,探讨LOX-1在泡沫细胞形成中的作用。方法:无菌分离、培养大鼠腹腔巨噬细胞,分别以终浓度10mg/L,25mg/L,50mg/L,75mg/L,100mg/L ox—LDL与巨噬细胞共孵育24h,以RT—PCR和Western blotting检测LOX-1基因表达水平;以终浓度75mg/L ox—LDL与巨噬细胞分别共孵育0.5h,3h,6h,12h,24h和36h后检测LOX-1表达水平;以不同浓度辛伐他汀预处理巨噬细胞后,再与ox-LDL共培养,检测LOX-1基因表达。结果:ox-LDL终浓度为10—75mg/L时,随着浓度增大,LOX-1mRNA和蛋白表达均增强,75mg/L时达高峰,ox-LDL 100mg/L时LOX-1表达显著降低(均P〈0.05);自ox-LDL与巨噬细胞共孵育6h开始,LOX-1表达逐渐增强,24h达高峰,36h时LOX-1表达下降(均P〈0.01);不同浓度辛伐他汀均使LOX-1表达降低,与对照组比较差异有统计学意义(P〈0.05)。结论:ox-LDL在一定范围内以剂量和时间依赖方式增强大鼠腹腔巨噬细胞LOX-1表达,LOX-1在巨噬细胞摄入ox-LDL的过程中可能具重要作用,辛伐他汀可抑制巨噬细胞LOX-1表达。 Objective To investigate the effect of ox - LDL on the expression of LOX - 1 in cultured celiac macrophages of rats and to explore the role of LOX - 1 in foam cell formation. Methods Celiac macrophages of rats were collected sterilely and co - incubated with ox - LDL for 24hrs, which final concentrations were 10 mg/L, 25 mg/L, 50 mg/L, 75mg/L and 100 mg/L respectively. Total RNA and protein were extracted ; LOX - 1 expressions were measured by RT - PCR and Western blotting respectively. Macrophages were cultured with ox- LDL (75mg/L) for 0. 5hrs, 3hrs, 6hrs, 12hrs, 24hrs and 36hrs respectively, then total RNA and protein were extracted, expressions of LOX - 1 were measured by RT - PCR and Western blotting. Macrophages were pretreated with different dosages of Simvastatin and then co - incubated with ox - LDL; expressions of LOX - 1 were also measured. Results Expressions of LOX - 1 increased gradually as the con- centration of ox -LDL increased between 10 N 75mg/L, reached the peak when the concentration was 75mg/L, and decreased dramatically when it was 100mg/L. Compared with control group, the differences of changes were significant ( P 〈0.05, either). After incubated with ox - LDL for 6hrs, the expressions of LOX - 1 began to increase gently and reach the peak at the 24hrs, and decreased after 36hrs. All the differences of changes were significant compared with control group ( P 〈0. 01 , either). Expressions of LOX - 1 were depressed by different dosages of Simvastatin and the differences were significant compared with control group ( P 〈 0. 05, either). Conclusion Ox - LDL increased the expression of LOX - 1 in celiac macrophages of rats in a dosage and time dependent manner. LOX - 1 may play a crucial role in the internalization of ox - LDL. Simvastatin can reduce the expression of LOX - 1.
作者 何军 马业新
出处 《中国医师杂志》 CAS 2007年第6期753-756,共4页 Journal of Chinese Physician
关键词 脂蛋白类 LDL 受体 泡沫细胞 斯伐他汀 药理学 Lipoproteins, LDL Receptors, LDL Poam cells Simvastatin/pharmacology
  • 相关文献

参考文献9

  • 1Miki Nagase, Shinya Kaname, Takashi Nagase, et al. Expression of LOX-1, an Oxidized Low-Density Lipoprotein Receptor, in Experimental Hypertensive Glomerulosclerosis. J Am Soc Nephrol, 2000, 11 : 1826- 1836. 被引量:1
  • 2Sawamura T, Kume N, Aoyama T, et al. An endothelial receptor for oxidized low-density lipoprotein. Nature, 1997, 386: 73-77. 被引量:1
  • 3Nagase M, Abe J, Takahashi K, et al. Genomie organization and regulation of expression of the lectinlike oxidized low-density lipoprotein receptor (LOX-1) gene. J Biol Chem, 1998, 273: 33702-33707. 被引量:1
  • 4Aoyama T, Fujiwara H, Masaki T, et al. Induction of lectin-like oxidized LDL receptor by oxidized LDL and lysophosphatidylcholine in cultured endothelial cells. J Mol Cell Cardiol, 1999, 31: 2101-2114. 被引量:1
  • 5Li DY, Yang BC, Mehta JL. Ox-LDL enhances anoxia-reoxygenation-mediated apoptosis in human coronary endothelial cells: Role of PKC, PTK, Bcl-2 and Fas. Am J Physiol, 1998, 275: H568-576. 被引量:1
  • 6Hanfang Zhang, Connie Snead, John D. Catravas. Nitric Oxide Differentially Regulates Induction of Type Ⅱ Nitric Oxide Synthase in Rat Vascular Smooth Muscle Cells Versus Macrophages. Arteriosclerosis, Thrombosis, and Vascular Biology,2001, 21 : 529-535. 被引量:1
  • 7JL Mehta. The role of LOX-1, a novel lectin-like receptor for oxidized low density lipoprotein, in atheroselerosis. Can J Cardiol. 2004, 20 (Suppl B) : 32B-36B. 被引量:1
  • 8严金川,吴宗贵,张玲珍,李莉,樊洁,凌玲,韩文余,张锁龙.OX-LDL及辛伐他汀对平滑肌细胞PKC活性和胞内Ca^(2+)的影响[J].中国病理生理杂志,2002,18(4):344-347. 被引量:3
  • 9Monaco C, Paleolog E. Nuclear factor Kappa B: a potential therapeutic target in atherosclerosis and thrombosis. Cardiovasc Res, 2004, 61: 671-682. 被引量:1

二级参考文献2

共引文献2

同被引文献15

  • 1何军,刘海潮,马业新.非对称二甲基精氨酸促进大鼠主动脉氧化型低密度脂蛋白受体表达[J].中国动脉硬化杂志,2006,14(12):1031-1034. 被引量:4
  • 2Kiyan Y, Tkachuk S, Hilfiker-Kleiner D, et al, oxLDL induces inflammatory responses in vascular smooth muscle ceils via urokinase receptor association with CD36 and TLR4. J Mol Cell Cardiol, 2013, 66c: 72-82. 被引量:1
  • 3Moriwaki H, Kume N, Sawamura T, et al. Ligand specificity of LOX- 1, a novel endothelial receptor for oxidized low density lipoprotein. Arterioscler Thromb Vasc Biol, 1998, 18:1541-1547. 被引量:1
  • 4Lusis A J, Atherosclerosis. Nature, 2000, 407:233-241. 被引量:1
  • 5May AE, Neumann FJ, Preissner KT. The relevance of blood cell vessel wall interactions for vascular thrombotic disease. Thromb Haemost, 1999, 82:962-970. 被引量:1
  • 6Go AS, Mozaffarian D, Roger VL, et al. Executive summary: heart disease and stroke statistics--2013 update: a report from the American Heart Association. Circulation, 2013, 127: 143-152. 被引量:1
  • 7Ross R. Atherosclerosis is an inflammatory disease. N Engl J Med , 1999,340 : 115- 126. 被引量:1
  • 8Edsfeldt A, Nitulescu M, Grufman H, et al. Soluble urokinase plasminugen activator receptor is associated with inflammation in the vulnerable human atherosclerotic plaque. Stroke, 2012, 43: 3305- 3312. 被引量:1
  • 9Dunn S, Vohra RS, Murphy JE, et al. The lectin-like oxidized low- density- lipoprotein receptor: a pro-inflammatory factor in vascular disease. Biochem J. 2008. 409: 349-355. 被引量:1
  • 10Mehta JL, Li DY. Identification and autoregulation of receptor for oxLDL in cultured human coronary artery endothelial cells. Biochem Biophys Res Commun, 1998, 248:511-514. 被引量:1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部