In vivo activity of nuclease-resistant siRNAs

被引:452
作者
Layzer, JM
McCaffrey, AP
Tanner, AK
Huang, Z
Kay, MA
Sullenger, BA [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Surg, Ctr Genet & Cellular Therapies, Durham, NC 27710 USA
[2] Stanford Univ, Sch Med, Dept Pediat, Program Human Gene Therapy, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Genet, Program Human Gene Therapy, Stanford, CA 94305 USA
关键词
RNAi; siRNA; modified nucleotides; luciferase;
D O I
10.1261/rna.5239604
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chemical modifications have been incorporated into short interfering RNAs (siRNAs) without reducing their ability to inhibit gene expression in mammalian cells grown in vitro. In this study, we begin to assess the potential utility of 2'-modified siRNAs in mammals. We demonstrate that siRNA modified with 2'-flouro (2'-F) pyrimidines are functional in cell culture and have a greatly increased stability and a prolonged half-life in human plasma as compared to 2'-OH containing siRNAs. Moreover, we show that the 2'-F containing siRNAs are functional in mice and can inhibit the expression of a target gene in vivo. However, even though the modified siRNAs have greatly increased resistance to nuclease degradation in plasma, this increase in stability did not translate into enhanced or prolonged inhibitory activity of target gene reduction in mice following tail vein injection. Thus, this study shows that 2'-F modified siRNAs are functional in vivo, but that they are not necessarily more potent than unmodified siRNAs in animals.
引用
收藏
页码:766 / 771
页数:6
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