Cellular Uptake and Intracellular Trafficking of Antisense and siRNA Oligonucleotides

被引:153
|
作者
Juliano, Rudolph L. [1 ]
Ming, Xin [1 ]
Nakagawa, Osamu [1 ]
机构
[1] Univ N Carolina, UNC Eshelman Sch Pharm, Div Mol Pharmaceut, Chapel Hill, NC 27599 USA
关键词
IN-VIVO DELIVERY; CLATHRIN-INDEPENDENT ENDOCYTOSIS; RECEPTOR-MEDIATED ENDOCYTOSIS; PROTEIN-COUPLED RECEPTOR; SHORT INTERFERING RNA; TAT-FUSION PROTEINS; PENETRATING PEPTIDES; MEMBRANE-FUSION; PHOSPHOROTHIOATE OLIGODEOXYNUCLEOTIDES; MAMMALIAN-CELLS;
D O I
10.1021/bc200377d
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Significant progress is being made concerning the development of oligonucleotides as therapeutic agents. Studies with antisense, siRNA, and other forms of oligonucleotides have shown promise in cellular and animal models and in some clinical studies. Nonetheless, our understanding of how oligonucleotides function in cells and tissues is really quite limited. One major issue concerns the modes of uptake and intracellular trafficking of oligonucleotides, whether as "free" molecules or linked to various delivery moieties such as nanoparticles or targeting ligands. In this review, we examine the recent literature on oligonucleotide internalization and subcellular trafficking in the context of current insights into the basic machinery for endocytosis and intracellular vesicular traffic.
引用
收藏
页码:147 / 157
页数:11
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