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肝内逆行胆管内输注质粒 DNA 和 DNA 纳米粒后,枯否细胞一过性耗竭可增强大鼠肝脏中的转基因表达。

Transient depletion of kupffer cells leads to enhanced transgene expression in rat liver following retrograde intrabiliary infusion of plasmid DNA and DNA nanoparticles.

机构信息

Department of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21205, USA.

出版信息

Hum Gene Ther. 2011 Jul;22(7):873-8. doi: 10.1089/hum.2010.146. Epub 2011 Mar 4.

Abstract

In this report, we have demonstrated that by temporarily removing Kupffer cells (KCs), the transgene expression levels mediated by retrograde intrabiliary infusion (RII) of plasmid DNA, polyethylenimine-DNA, and chitosan nanoparticles were enhanced by 1,927-, 131-, and 23,450-fold, respectively, in comparison with the respective groups without KC removal. KC removal also led to significantly prolonged transgene expression in the liver that received all three carriers. This increased transgene expression was correlated with significantly reduced serum tumor necrosis factor-α level as an indicator for KC activation. These results suggest that KC activation is a significant contributing factor to the lowered transgene expression by polycation-DNA nanoparticles delivered by RII. More importantly, the combination of RII and transient removal of KCs may be adopted as an effective approach to achieving high and persistent transgene expression in the liver mediated by nonviral nanoparticles.

摘要

在本报告中,我们证明了通过暂时去除库普弗细胞(KCs),与未去除 KC 的相应组相比,逆行胆管内输注(RII)质粒 DNA、聚乙烯亚胺-DNA 和壳聚糖纳米粒介导的转基因表达水平分别增强了 1927 倍、131 倍和 23450 倍。KC 去除还导致接受所有三种载体的肝脏中转基因表达显著延长。这种增加的转基因表达与作为 KC 激活指标的血清肿瘤坏死因子-α水平的显著降低相关。这些结果表明,KC 的激活是 RII 递送的聚阳离子-DNA 纳米颗粒降低转基因表达的一个重要因素。更重要的是,RII 与 KC 的短暂去除相结合,可能被采用作为通过非病毒纳米颗粒在肝脏中实现高和持续转基因表达的有效方法。

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