Down-regulation of IL-8 expression in human airway epithelial cells through helper-dependent adenoviral-mediated RNA interference

被引:24
作者
Cao, HB
Wang, AA
Martin, B
Koehler, DR
Zeitlin, PL
Tanawell, AK
Hu, J
机构
[1] Hosp Sick Children, Programme Lung Biol Res, Toronto, ON M5G 1X8, Canada
[2] Hosp Sick Children, Canadian Inst Hlth Res Grp Lung Dev, Toronto, ON M5G 1X8, Canada
[3] Univ Toronto, Dept Paediat, Toronto, ON M5S 1A1, Canada
[4] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A1, Canada
[5] Univ Toronto, Lab Med & Pathobiol, Toronto, ON M5S 1A1, Canada
[6] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21287 USA
基金
加拿大健康研究院;
关键词
interleukin-8; RNA interference; helper-dependent adenoviral vector; inflammation; chemokine; neutrophil; cystic fibrosis;
D O I
10.1038/sj.cr.7290275
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Interleukin (EL)-8 is a potent neutrophil chemotactic factor and a crucial mediator in neutrophil-dependent inflammation. Various cell types produce IL-8, either in response to external stimuli such as cytokines or bacterial infection, or after malignant transformation. Anti-IL-8 strategies have been considered for anti-inflammatory therapy. In this paper we demonstrate that the RNA interference technique can be used to efficiently down-regulate IL-8 protein expression in airway epithelial cells. We used a helper-dependent adenoviral vector to express a small hairpin (sh)RNA targeting human IL-8 in cultured airway epithelial cells (IB3-1, Cftr(-/-); C38, Cftr-corrected) stimulated with TNF-alpha, IL-1 beta or heat-inactivated Burkholderia cenocepacia. Stimulated IL-8 expression in IB3-1 and C38 cells was significantly reduced by shRNA expression. The shRNA targeting IL-8 had no effect on the activation of NF-kappa B, or on the protein levels of I kappa B or IL-6, suggesting that this anti-IL-8 strategy was highly specific, and therefore may offer potential for the treatment of inflammatory diseases.
引用
收藏
页码:111 / 119
页数:9
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