期刊文献+

冠心病患者巨噬细胞肝X受体的活化与胆固醇外流 被引量:2

Liver X receptor activation and cholesterol efflux in macrophages from coronary atherosclerotic disease patients
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摘要 目的:研究冠心病患者巨噬细胞肝X受体(LXR)及其下游的一些目的基因表达和胆固醇外流特点。方法:分离冠心病患者组和对照组外周血的单核细胞,并转化为巨噬细胞。在TO-901317的刺激下,观察巨噬细胞的aopA-I介导胆固醇外流的变化和LXR以及其下游一些目的基因的mRNA表达。结果:冠心病患者的巨噬细胞,其一些影响胆固醇代谢及炎症反应的基因表达受到了影响,aopA-I介导的胆固醇外流能力下调,对刺激LXR后的反应性也降低。结论:冠心病患者的巨噬细胞胆固醇外流功能下降,其一些影响胆固醇代谢及炎症反应的基因表达发生了改变,对刺激LXR信号的反应性下降。提示巨噬细胞的LXR信号途径可能是冠心病发病机制中的重要环节,也是冠心病治疗潜在靶点。 AIM : To study the characteristic of liver X receptor alpha (LXRct) , it's target gene expression and cholesterol efflux from human macrophages in coronary atherosclerotic disease (CAD) patients. METHODS: Human monocyte - derived macrophages from CAD patients and controls were collected. Before being detected apoA - I - mediated human monocyte - derived macrophage cholesterol efflux and LXRα and mRNA expression of its target gene, the macrophages were induced with or without TO -901317. RESULTS: Compared with control normal macrophage, the mRNA levels of LXRα and its target gene expression were changed, and the macrophage cholesterol efflux was decreased in CAD patients. After stimulationwith TO -901317, the reactive capacity of LXR was also decreased from human monocyte - derived macrophage of CAD patients. CONCLUSION: The changes of cholesterol eftlux and some gene expression in macrophages may be the pathogenetic cause atherosclerosis, and macrophage LXR activity may offer potential therapeutic benefit in the treatment of CAD.
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2006年第11期2146-2150,共5页 Chinese Journal of Pathophysiology
关键词 冠状动脉疾病 胆固醇外流 巨噬细胞 受体 肝X Coronary disease Cholesterol efflux Macrophages Receptors, liver X
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参考文献11

  • 1Lusis AJ.Atherosclerosis[J].Nature,2000,407(6801):233-241. 被引量:1
  • 2Febbraio M.Targeted disruption of the class B scavenger receptor CD36 protects against atherosclerotic lesion development in mice[J].J Clin Invest,2000,105(8):1049-1056. 被引量:1
  • 3Suzuki H.A role for macrophage scavenger receptors in atherosclerosis and susceptibility to infection[J].Nature,1997,386(6622):292-295. 被引量:1
  • 4Whitney KD,Watson MA,Goodwin B,et al.Liver X receptor (LXR) regulation of the LXRα gene in human macrophages[J].J Biol Chem,2001,276(47):43509-43515. 被引量:1
  • 5Joseph SB,Castrillo A,Laffitte BA,et al.Reciprocal regulation of inflammation and lipid metalolism by liver X receptors[J].Nature Medicine,2003,9(2):213-219. 被引量:1
  • 6Ricote M,Valledor AF,Glass CK.Decoding transcriptional programs regulated by PPARs and LXRs in the macrophage:effects on lipid homeostasis,inflammation,and atherosclerosis[J].Arterioscler Thromb Vasc Biol,2004,24(2):230-239. 被引量:1
  • 7Luo Y,Tall AR.Sterol upregulation of human CETP expression in vitro and in transgenic mice by an LXR element[J].J Clin Invest,2000,105(36):513-520. 被引量:1
  • 8Scanlon PJ,Faxon DP,Audet AM,et al.ACC/AHA guidelines forcoronary angiography:A report of the American College of Cardiology/American Heart Association task force on practice guidelines (committee on coronary angiography)[J].JACC,1999,33(6):1756-1824. 被引量:1
  • 9Suzuki S,Tomoko NM,Tamehiro N,et al.Verapamil increases the apolipoprotein-mediated release of cellular cholesterol by induction of ABCA1 expression via liver X receptor-independent mechanism[J].Arterioscler Thromb Vasc Biol,2004,24(3):519-525. 被引量:1
  • 10Lin GR,Bornfeldt KE.Cyclic AMP-specific phosphodiesterase 4 inhibitors promote ABCA1 expression and cholesterol efflux[J].Biochem Biophys Res Commun,2002,290(2):663-669. 被引量:1

同被引文献12

  • 1WANG L, BAO Y, YANG Y, et al. Discovery of antagonists for human scavenger receptor CD36 via an ELISA-like high-throughput screening assay[J]. J Biomol Screen,2010,15:239-250. 被引量:1
  • 2SUZUKI S, TOMOKO N M, TAMEHIRO N, et al. Verapamil increases the apolipoprotein-mediated release of cellular cholesterol by induction of ABCA1 expression via liver X receptor-independent mechanism[J]. Arterioscler Thromb Vasc Biol, 2004,24 : 519 - 525. 被引量:1
  • 3LING R, BORNFELDT K E. Cyclic AMP-specific phos- phodiesterase 4 inhibitors promote ARCA1 expression and cholesterol efflux[J]. Biochemical and Biophysical Research Communications, 2002,290: 663- 669. 被引量:1
  • 4SUZUKI S, TOMOKO N M, TAMEHIRO N, et al. Verapamil increases the apolipoprotein-mediated release of cellular cholesterol by induction of ABCA1 expression via liver X receptor-independent mechanism[J]. Arterioscler Thromb Vasc Biol, 2004,24 : 519- 525. 被引量:1
  • 5VON ECKARDSTEIN A, NOFER J R, ASSMANN G. High density lipoproteins and arteriosclerosis. Role of cholesterol efflux and reverse cholesterol transport[J]. Arterioscler Thromh Vasc Biol, 2001, 21:13-27. 被引量:1
  • 6LIBBY P, OKAMOTO Y, ROCHA V Z, et al. Inflammation in atherosclerosis: Transition from theory to practice[J]. Circ J, 2010,74 : 213 - 220. 被引量:1
  • 7LEVIN N, BISCHOFF E D, DAIGE C L, et al. Macrophage liver X receptor is required for antiatherogenic activi- ty of LXR agonists[J]. Arterioscler Thromb Vasc Biol, 2005,25:135- 142. 被引量:1
  • 8钱一欣,倪兆慧.肝X受体在代谢和炎症中的作用[J].临床心血管病杂志,2007,23(11):806-810. 被引量:3
  • 9无.绝经后女性血脂异常管理的中国专家共识[J].中华心血管病杂志,2014,42(4):279-283. 被引量:50
  • 10曾新颖,齐金蕾,殷鹏,王黎君,刘韫宁,刘江美,周脉耕,梁晓峰.1990~2016年中国及省级行政区疾病负担报告[J].中国循环杂志,2018,33(12):1147-1158. 被引量:71

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