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林娜, 单毓娟, 赵瑞芳, 袁超, 王舒然. 莱菔硫烷对血管内皮细胞粘附分子表达影响[J]. 中国公共卫生, 2009, 25(3): 329-331. DOI: 10.11847/zgggws2009-25-03-40
引用本文: 林娜, 单毓娟, 赵瑞芳, 袁超, 王舒然. 莱菔硫烷对血管内皮细胞粘附分子表达影响[J]. 中国公共卫生, 2009, 25(3): 329-331. DOI: 10.11847/zgggws2009-25-03-40
LIN Na, SHAN Yu-juan, ZHAO Rui-fang, . Effects of sulforaphane on expressions of ICAM-1 and VCAM-1 mRNA induced by LPS and nuclear translocation of NF-κB in vascular endothelial cell[J]. Chinese Journal of Public Health, 2009, 25(3): 329-331. DOI: 10.11847/zgggws2009-25-03-40
Citation: LIN Na, SHAN Yu-juan, ZHAO Rui-fang, . Effects of sulforaphane on expressions of ICAM-1 and VCAM-1 mRNA induced by LPS and nuclear translocation of NF-κB in vascular endothelial cell[J]. Chinese Journal of Public Health, 2009, 25(3): 329-331. DOI: 10.11847/zgggws2009-25-03-40

莱菔硫烷对血管内皮细胞粘附分子表达影响

Effects of sulforaphane on expressions of ICAM-1 and VCAM-1 mRNA induced by LPS and nuclear translocation of NF-κB in vascular endothelial cell

  • 摘要: 目的 研究莱菔硫烷对脂多糖诱导的人脐静脉内皮细胞(ECV304)的细胞中粘附分子(ICAM-1)和血管细胞粘附分子-1(VCAM-1)mRNA表达影响以及转录机制。方法 采用ECV304细胞为研究对象,用实时定量PCR方法(real-time PCR)检测ICAM-1和VCAM-1的mRNA表达水平,用免疫荧光法检测转录因子(NF-κB)向核内转位的情况。结果 用5,10,20μmol/L莱菔硫烷作用再用脂多糖刺激,细胞中ICAM-1mRNA表达量下降,分别为对照组的2.3,1.5和1.1倍,呈一定剂量-效应关系,与脂多糖组比较,差异均有统计学意义(均P<0.05);5μmol/L莱菔硫烷能使脂多糖诱导的VCAM-1 mRNA表达降低为1.4倍,而10,20μmol/L莱菔硫烷则完全抵消了脂多糖对VCAM-1 mRNA的诱导,2组VCAM-1 mRNA的表达均降低为对照组的0.4倍,与脂多糖组比较,差异均有统计学意义(均P<0.05);10μmol/L莱菔硫烷作用后,细胞核中绿色荧光明显弱于脂多糖单独处理组,表明莱菔硫烷可抑制脂多糖诱导的NF-κB的核转位。结论 莱菔硫烷可通过阻断NF-κB的核转位来抑制脂多糖诱导的ECV304细胞ICAM-1和VCAM-1 mRNA的表达。

     

    Abstract: Objective To study the effects of sulforaphane on the expressions of ICAM-1 and VCAM-1 mRNA induced by lipopoly saccharide(LPS)in vascular endothelial cell ECV 304 and its tran scriptional mechanism.Methods The levels of mRNA of ICAM-1 and VCAM-1 were determined by quantitative real-tmie PCR and nuclear translocation of NF-κB was measured by immunofluorescence hybridization.Results Treated with 5,10,20 mol/L sulforaphane followed by LPS,the expressions of ICAM-1 mRNA in ECV 304 were deminished to 2.3,1.5 and 1.1 fold of the level of the control,respectively.Compared with LPS,sulforaphane significantly inhibited the expression of ICAM-1 mRNA in dose-dependent manner(P<0.05).5 mol/L sulforaphane down-regulated expression of VCAM-1 mRNA induced by LPS to 1.4 fold,while 10,20 mol/L sulforaphane completely elmiinated the stmiulation and the level of VCAM-1 mRNA was only 0.4 fold of the control(P<0.05).The weakness of the strength of green fluore scence in nuclear indicated that 10 mol/L sulforaphane could block the translocation of NF-κB.Conclusion Sulforaphane down-regulates the expression of ICAM-1 and VCAM-1 mRNA through blocking the translocation of NF-κB into nucleus.

     

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