同型半胱氨酸对单核细胞NF-κB活化及巨噬细胞炎性蛋白-1α表达的影响

被引:5
作者
邢玮
邓仲端
瞿智玲
倪娟
机构
[1] 华中科技大学同济医学院病理学系,华中科技大学同济医学院病理学系,华中科技大学同济医学院病理学系,华中科技大学同济医学院病理学系武汉,武汉,武汉,武汉
关键词
高同种半胱氨酸血症; 抑制蛋白类; NF-κB; 动脉硬化;
D O I
暂无
中图分类号
R543 [血管疾病];
学科分类号
1002 ; 100201 ;
摘要
目的 探讨同型半胱氨酸对体外培养的人单核细胞株THP -1核因子-κB(NF -κB)、抑制因子(IκB- α)活性的影响及其与巨噬细胞炎性蛋白-1α(MIP- 1α)表达上调的关系。方法 THP -1单核细胞分别用同型半胱氨酸和NF- κB抑制剂PDTC预处理后,应用Northernblot和流式细胞术分别检测MIP- 1αmRNA和蛋白的表达,并应用Western蛋白印迹进一步检测核蛋白NF -κB蛋白含量和胞质IκB -α含量。结果 与未加任何处理因素的对照组比较,MIP- 1αmRNA和蛋白在0. 1mmol/L同型半胱氨酸处理后明显增加,分别为对照组的3 .69倍和1 .16倍(P<0 .01),同时NF κBP65亚基核转位亦增加。而加入100μmol/LNF κB抑制剂PDTC预处理30min后,再用同样浓度的同型半胱氨酸刺激,则MIP -1αmRNA和蛋白表达受到明显的抑制,NF- κBP65核转位增加。单独加入PDTC对MIP -1αmRNA、蛋白表达及NF -κBP65核转位无明显影响。此外,同型半胱氨酸( 0 .1mmol/L)处理THP- 1可引起IκB -α蛋白水平显著降低, 120min后有所回升。结论 同型半胱氨酸在病理浓度可促进NF -κB活化,发生核转位,进而促进THP -1细胞表达MIP 1αmRNA和蛋白,这种作用与IκB -α蛋白磷酸化降解有关。
引用
收藏
页码:101 / 104
页数:4
相关论文
共 16 条
[1]  
Genomic cloning and promoter analysis of macrophage inflammatory protein ( MIP) -2 ,MIP-1 alpha, and MIP-1 beta, members of the chemokine superfamily of proinflammatory cytokines. Widmer U,Manogue KR,Cerami A,et al. J Immunol . 1993
[2]  
The pathogenesis of atherosclerosis: a perspective for the 1990s. Ross R. Nature . 1993
[3]  
Homocysteine and cardiovascular disease. Kalra DK. Current Atherosclerosis Reports . 2004
[4]  
The association of homocysteine and coronary artery disease. Gauthier GM,Keevil JG,McBride PE. Clinical Cardiology . 2003
[5]  
Chemokines and atherosclerosis. Sheikine Y,Hansson GK. Annals of Medicine . 2004
[6]  
Monocyte chemoattractant protein-1 induces proliferation and interleukin-6 production in human smooth muscle cells by differential activation of nuclear factor-kappaB and activator protein-1. Viedt C,Vogel J,Athanasiou T,et al. Arteriosclerosis and Thrombosis . 2002
[7]  
Endothelial nuclear factor-kappa B and the initiation of the atherosclerotic lesion. Collins T. Laboratory Investigation . 1993
[8]  
Homocysteine-induced endoplasmic reticulum stress and growth arrest leads to specific changes in gene expression in human vascular endothelial cells. Outinen PA,Sood SK,Pfeifer SI,et al. Blood . 1999
[9]  
Pyrrolidine dithiocarbamate augments IL-10,inhibits TNF-alpha, MIP-1 alpha,IL-12 and ni-tricoxide production and protects from the lethal effect of endotoxin. Nemeth ZH,Hasko G,Vizi ES. Shock . 1998
[10]  
Rapid detection of octamer binding proteins with ‘miniextracts’prepared from a small number of cells. Schreiber E,Matthias P,Muller MM,et al. Nucleic Acids Research . 1989