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LPS对心脏微血管内皮细胞ICAM-1表达的影响及rHDL的调控作用 被引量:4

EFFECTS OF LPS AND rHDL ON EXPRESSION OF ICAM-1 IN CARDIAC MICROVASCULAR ENDOTHELIAL CELLS
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摘要 目的:观察 PLS作用下心脏微血管内皮(CMECs)细胞间粘附分子 (ICAM)-1的表达情况及rHDL的调控作用,为CHD的防治提供实验依据。方 法:利用培养的血管内皮细胞,采用流式细胞仪检测正常细胞、LPS作用和LPS与 rHDL协同作用下0、1、2、6、12小时不同时相点 ICAM-1表达阳性细胞数及荧光 强度。结果:LPS和CMECs共同孵育下,随时间延长ICAM-1表达的阳性细胞数 和荧光强度上升,rHDL有抑制ICAM-1表达作用。结论:PLS可以刺激CMECs 表达ICAM-1,rHDL对血管内波细胞的损伤有保护作用。 Objective: To investigate the effects of LPS and recombinant high density lipoprotein(rHDL) on the expression of intercellular adhesion molecule 1(ICAM-1) in cardiac microvascular endothelial cells(CMECs) to provide theoretic basis for prevention and treatment of coronary heart disease(CHD). Methods: After the cardiac microvascular endothelial cells were extracted,they were randomized into three groups(A,B and C). The cells in group A were routinely cultured while those in groups B and C were respectively cultured in the media with addition of LPS and rHDL. Then the number of cells with positive expression of ICAM-1 and florescent density of the expression were determined in 0,1,2,6 and 12h after incubation with flow cytometry. Results: After the CMECs were incubated in the medium with addition of LPS,the number of the cells with positive expression of ICAM-1 and florescent density of the expression were gradually increased with time prolongation. And rHDL could inhibit the expression of ICAM-1. Condclusion: LPS can stimulate CMECs to express ICAM-1 and rHDL might protect the vasular endothelial cells from damage.
出处 《中国血液流变学杂志》 CAS 1999年第1期10-12,共3页 Chinese Journal of Hemorheology
关键词 心脏 微血管 内皮细胞 冠心病 LPS rHDL intercellular adhesion molecule 1 cardiac microvascular endothelial cell
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  • 1张向鑫,李庆浩,李清.P-选择素与心肌缺血再灌注损伤[J].社区医学杂志,2004,2(3):26-28. 被引量:6
  • 2刘滨,李红莉,刘阳,周令望,于维汉.大鼠急性心肌损伤E选择素和细胞因子的变化[J].中国地方病学杂志,2005,24(2):158-160. 被引量:8
  • 3饶丹,姜红,曾秋棠.黏附分子细胞间黏附分子-1/E-选择素与冠心病[J].心血管病学进展,2005,26(3):278-281. 被引量:14
  • 4贾俊海,陈素仙,苏一星,范廷潞,张茜,刘可琢.灯盏花素对大鼠心肌缺血再灌注损伤的保护作用[J].江苏大学学报(医学版),2006,16(6):477-480. 被引量:21
  • 5Mason DP,Kenagy RD,Hasenstab D,et al.Matrix metallop-roteinase-9 overexpression enhances vascular smooth muscle cell migration and alters remodeling in the injured rat carotid artery[J].Circ Res, 1999,85:1179.
  • 6Aesim CH, Michael A.Matrix metalloproteinase-9 is necessary for the regulation of smooth muscle cell replication and migration after arterial injury[J].Circ Res,2002,91:845.
  • 7Duharme A, Fratz S,Aikawa M,et al.Targeted deletion of matrix metalloproteinase-9 attenuates left ventricular enlargement and collagen accumulation after experiment myocardial infarction[J].J Clin Invest,2000,106:55.
  • 8Inokubo Y,Hanada H, Ishizaka H, et al.Plasmalevels of matrix metallopeotein-9 and tissue inhibitor of matalloproteinase-9 are increased in the coronary circulation in patiens with acute coronary syndrome[J].Am Heart J, 2001,142:211.
  • 9Ross R. Atherosclerosis-An inflammatory disease[J].N Engl J Med, 1999,340:115.
  • 10Ortego M, Bustos C,Hemandez-Presa MA, et al.Atorvastatin reduces NF-κB activation and chemokine expression in vascular smooth muscle cells and mononuclear cells[J].Atherosclerosis, 1999,147:253-261.

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