Inhibition of NF-κB mediated inflammation by siRNA expressed by recombinant adeno-associated virus

被引:39
作者
Pinkenburg, O [1 ]
Platz, J [1 ]
Beisswenger, C [1 ]
Vogelmeier, C [1 ]
Bals, R [1 ]
机构
[1] Univ Marburg, Hosp Univ Marburg, Div Pulm Dis, Dept Internal Med, D-35043 Marburg, Germany
关键词
recombinant adeno-associated virus; small inhibitory RNA; RNA interference; gene silencing; inflammation;
D O I
10.1016/j.jviromet.2004.04.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
NF-kappaB mediated inflammation is a key process to many diseases. RNA interference (RNAi) is the specific suppression of genes by short double-stranded RNA. It was the aim of the present study to modify NF-kappaB-dependent inflammation by small interfering RNA (siRNA) expressed by recombinant adeno-associated virus (rAAV). To study the kinetics of rAAV mediated expression of siRNA, the expression of the luciferase, gene was targeted and resulted in a significant decrease of luciferase activity as compared to a control vector in the human 293 cell line. The effect was dose dependent and was detectable 24 h after infection. rAAV coding for siRNA against the p65 subunit of NF-kappaB significantly reduced the p65 protein. In a cellular model of TNF-alpha induced inflammation, expression of siRNA against p65 significantly suppressed the secretion of IL-8 from BEAS-2B cells. In conclusion, rAAV vectors coding for siRNA are an useful tool for efficient gene silencing in mammalian cells and can be used to modify NF-kappaB mediated inflammation. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:119 / 122
页数:4
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