Click-Modified Anandamide siRNA Enables Delivery and Gene Silencing in Neuronal and Immune tells

被引:61
|
作者
Willibald, Julian [1 ]
Harder, Johannes [1 ]
Sparrer, Konstantin [2 ,3 ]
Conzelmann, Karl-Klaus [2 ,3 ]
Carell, Thomas [1 ]
机构
[1] Univ Munich, Ctr Integrated Prot Sci, Dept Chem, D-81377 Munich, Germany
[2] Univ Munich, Max Von Pettenkofer Inst, D-81377 Munich, Germany
[3] Univ Munich, Gene Ctr, D-81377 Munich, Germany
关键词
INTRACELLULAR DELIVERY; RNA-INTERFERENCE; CATIONIC LIPIDS; ANTISENSE OLIGONUCLEOTIDE; CELLULAR UPTAKE; RECEPTOR; SYK; CONJUGATION; EXPRESSION; CHEMISTRY;
D O I
10.1021/ja303251f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Click chemistry of alkyne-modified RNA with different receptor ligand azides was used to prepare 3'-folate, 3'-cholesterol, and, as a new entity, 3'-anandamide-modified RNA in high yields and excellent purity. The anandamide-modified RNA shows surprisingly high transfection properties and enables the delivery of siRNA even into difficult-to-transfect RBL-2H3 cells which model neuronal uptake. Furthermore, the system was employed in human immune cells (BJAB), demonstrating silencing effects similar to those of a cationic, benchmark transfection reagent. In addition, the anandamide conjugates were found to be nontoxic. The reported chemistry and the described properties of the anandamide siRNA extend the possibilities of using siRNA-based gene silencing in neuronal and immune cells.
引用
收藏
页码:12330 / 12333
页数:4
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