Silencing microRNA by interfering nanoparticles in mice

被引:44
作者
Su, Jie [1 ]
Baigude, Huricha [1 ,2 ]
McCarroll, Joshua [1 ]
Rana, Tariq M. [1 ,2 ]
机构
[1] Univ Massachusetts, Dept Mol Pharmacol & Biochem, Sch Med, Worcester, MA 01605 USA
[2] Sanford Burnham Med Res Inst, Program RNA Biol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
TARGET MESSENGER-RNAS; C VIRUS-INFECTION; IN-VIVO; ANIMAL DEVELOPMENT; NONHUMAN-PRIMATES; THERAPEUTIC RNAI; MODIFIED SIRNAS; REPLICATION; DISEASE; LIVER;
D O I
10.1093/nar/gkq1307
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
MicroRNAs (miRNAs) are small endogenous non-coding RNAs that regulate post-transcriptional gene expression and are important in many biological processes. Disease-associated miRNAs have been shown to become potential targets for therapeutic intervention. Functions of miRNAs can be inhibited by using antisense oligonucleotides, called anti-miRs, complimentary to the miRNA sequences. Here, we show that systemic delivery of a chemically stabilized anti-miR-122 complexed with interfering nanoparticles (iNOPs) effectively silences the liver-expressed miR-122 in mice. Intravenous administration of 2 mg kg(-1) chemically modified anti-miR-122 complexed with iNOP-7 resulted in 83.2 +/- 3.2% specific silencing of miR-122, which was accompanied by regulating gene expression in liver and lowering of plasma cholesterol. The specific silencing of miR-122 was long lasting and did not induce an immune response. Our results demonstrate that iNOPs can successfully deliver anti-miR to specifically target and silence miRNA in clinically acceptable and therapeutically affordable doses.
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页数:6
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