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siRNA干扰明胶酶对人肾小管细胞ICAM-1表达的影响
引用本文:梅艳,洪权,张雪光,丁瑞,陈香美.siRNA干扰明胶酶对人肾小管细胞ICAM-1表达的影响[J].解放军医学杂志,2007,32(7):697-700.
作者姓名:梅艳  洪权  张雪光  丁瑞  陈香美
作者单位:100853,北京,解放军总医院肾科,解放军肾病中心暨全军重点实验室
基金项目:国家重点基础研究发展计划(973计划) , 国家自然科学基金 , 国家自然科学基金
摘    要:目的 利用小干扰RNA(siRNA)抑制人肾小管上皮细胞(HKC)的基质金属蛋白酶-2(MMP-2)和MMP-9,即明胶酶A和B的表达,观察其对胞间黏附分子1(ICAM-1)表达的影响.方法 培养人肾小管上皮细胞,以100nmol/L佛波醇酯(PMA)刺激18h,脂质体转染抑制MMP-2或MMP-9表达的siRNA或无关siRNA.提取细胞总RNA或胞浆蛋白,利用Real-Time PCR、Western blot或免疫荧光结合激光共聚焦显微镜技术检测MMP-2、MMP-9或ICAM-1的表达情况.结果 特异性的siRNA能有效抑制HKC中MMP-2、MMP-9的mRNA和蛋白表达;免疫荧光结果显示经PMA刺激后HKC的ICAM-1表达上调,同时MMP-9-siRNA转染组人肾小管细胞的ICAM-1蛋白表达水比其他实验组高(P<0.05).结论 抑制肾小管上皮细胞MMP-9的表达可使ICAM-1表达上调,提示除了细胞外基质降解途径外,MMP-9还可通过炎症途径影响肾脏纤维化进程.

关 键 词:基质金属蛋白酶类  胞间黏附分子1  RNA干扰  siRNA  干扰  明胶酶  肾小管细胞  表达上调  影响  renal  tubular  epithelial  cells  human  expression  effect  肾脏纤维化  炎症  降解途径  细胞外基质  肾小管上皮细胞  实验组  水比  转染  显示  蛋白表达
修稿时间:2007-03-082007-06-15

Intervention of siRNA to the effect of gelatinase on the expression of ICAM-1 in human renal tubular epithelial cells
Mei Yan, Hong Quan, Zhang Xueguang,et al..Intervention of siRNA to the effect of gelatinase on the expression of ICAM-1 in human renal tubular epithelial cells[J].Medical Journal of Chinese People's Liberation Army,2007,32(7):697-700.
Authors:Mei Yan  Hong Quan  Zhang Xueguang  
Institution:Department of Nephrology, Institute of Nephrology and Key Lab of Chinese PLA, General Hospital of PLA, Beijing 100853, China
Abstract:Objective To inhibit the expression of matrix metalloproteinase-2(MMP-2) and matrix metalloproteinase-9(MMP-9) in human kidney tubular epithelial cell(HKC) with specific small interference RNA(siRNA),then to observe whether the expression of intercellular adhesion molecule-1(ICAM-1) on HKC could be influenced.Methods HKCs were transfected with MMP-2,MMP-9 siRNA or irrespective siRNA respectively,untransfected HKC was considered as blank control.Four groups of HKCs were stimulated with 100nmol/L phorbol myristate acetate(PMA) for 18h.Total RNA or protein of cells were extracted with Trizol and RIPA cell lysate respectively,the mRNA expression levels of MMP-2,MMP-9 and ICAM-1 were detected by real time PCR,the protein expression levels of above indexes were detected by western blotting and immunofluorescence combined with confocal laser microscopy.Results The specific siRNA could inhibit the expression of MMP-2 and MMP-9 in HKCs effectively.Immunofluorescence combined with confocal assay demonstrated that while HKCs was stimulated with PMA,the expression of ICAM-1 was up-regulated,which was significantly up-regulated in the group transfected with MMP-9 siRNA(P<0.05).However,there was no significant difference among the groups transfected with MMP-2 siRNA,irrespective siRNA and untransfected group(P>0.05).Conclusions The inhibitory expression of MMP-9 of HKC may up-regulate the expression of ICAM-1,implying that,besides taking part in the degradation of extracellular matrix,MMP-9 may throw an influence on the proceeding of renal fibrosis by inflammatory pathway.
Keywords:matrix metalloproteinases  intercellular adhesion molecule- 1  RNA interference
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