Biophysical and structural characterization of polyethylenimine-mediated siRNA delivery in vitro

被引:282
作者
Grayson, Amy C. Richards
Doody, Anne M.
Putnam, David
机构
[1] Cornell Univ, Dept Biomed Engn, Ithaca, NY 14853 USA
[2] Cornell Univ, Sch Chem & Biomol Engn, Ithaca, NY 14853 USA
关键词
luciferases; polyethylenimine; RNA interference; small interfering RNA; transfection;
D O I
10.1007/s11095-006-9009-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. The goals of this study were as follows: 1) to evaluate the efficacy of different polyethylenimine (PEI) structures for siRNA delivery in a model system, and 2) to determine the biophysical and structural characteristics of PEI that relate to siRNA delivery. Materials and Methods. Biophysical characterization (effective diameter and zeta potential), cytotoxicities, relative binding affinities and in vitro transfection efficiencies were determined using nanocomplexes formed from PEI's of 800, 25,000, (both branched) and 22,000 (linear) molecular weights at varying N:P ratios and siRNA concentrations. The HR5-CL11 cell line stably expressing luciferase was used as a model system in vitro. Results. Successful siRNA delivery was observed within a very narrow window of conditions, and only with the 25,000 branched PEI at an N:P ratio of 6:1 and 8:1 and with 200 nM siRNA. While the zeta potential and size of PEI:siRNA complexes correlated to transfection efficacy in some cases, complex stability may also affect transfection efficacy. Conclusions. The ability of PEI to transfer functionally active siRNA to cells in culture is surprisingly dependent on its biophysical and structural characteristics when compared to its relative success and ease of use for DNA delivery.
引用
收藏
页码:1868 / 1876
页数:9
相关论文
共 51 条
[21]   Size, diffusibility and transfection performance of linear PEI/DNA complexes in the mouse central nervous system [J].
Goula, D ;
Remy, JS ;
Erbacher, P ;
Wasowicz, M ;
Levi, G ;
Abdallah, B ;
Demeneix, BA .
GENE THERAPY, 1998, 5 (05) :712-717
[22]   Effect of vector-expressed shRNAs on hTERT expression [J].
Guo, Ying ;
Liu, Jun ;
Li, Ying-Hui ;
Song, Tian-Bao ;
Wu, Jing ;
Zheng, Cai-Xia ;
Xue, Cai-Fang .
WORLD JOURNAL OF GASTROENTEROLOGY, 2005, 11 (19) :2912-2915
[23]   An RNA-directed nuclease mediates post-transcriptional gene silencing in Drosophila cells [J].
Hammond, SM ;
Bernstein, E ;
Beach, D ;
Hannon, GJ .
NATURE, 2000, 404 (6775) :293-296
[24]  
Harper SQ, 2005, METH MOL B, V309, P219
[25]   Lipid-mediated siRNA delivery down-regulates exogenous gene expression in the mouse brain at picomolar levels [J].
Hassani, Z ;
Lemkine, GF ;
Erbacher, P ;
Palmier, K ;
Alfama, G ;
Giovannangeli, C ;
Behr, JP ;
Demeneix, BA .
JOURNAL OF GENE MEDICINE, 2005, 7 (02) :198-207
[26]   Sequence-specific potent induction of IFN-α by short interfering RNA in plasmacytoid dendritic cells through TLR7 [J].
Hornung, V ;
Guenthner-Biller, M ;
Bourquin, C ;
Ablasser, A ;
Schlee, M ;
Uematsu, S ;
Noronha, A ;
Manoharan, M ;
Akira, S ;
de Fougerolles, A ;
Endres, S ;
Hartmann, G .
NATURE MEDICINE, 2005, 11 (03) :263-270
[27]   Sequence-dependent stimulation of the mammalian innate immune response by synthetic siRNA [J].
Judge, AD ;
Sood, V ;
Shaw, JR ;
Fang, D ;
McClintock, K ;
MacLachlan, I .
NATURE BIOTECHNOLOGY, 2005, 23 (04) :457-462
[28]   Low-molecular-weight polyethylenimine as a non-viral vector for DNA delivery: comparison of physicochemical properties, transfection efficiency and in vivo distribution with high-molecular-weight polyethylenimine [J].
Kunath, K ;
von Harpe, A ;
Fischer, D ;
Peterson, H ;
Bickel, U ;
Voigt, K ;
Kissel, T .
JOURNAL OF CONTROLLED RELEASE, 2003, 89 (01) :113-125
[29]   Synergistic effect of polyethylenimine and cationic liposomes in nucleic acid delivery to human cancer cells [J].
Lee, CH ;
Ni, YH ;
Chen, CC ;
Chou, CK ;
Chang, FH .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1611 (1-2) :55-62
[30]   Expression of small interfering RNAs targeted against HIV-1 rev transcripts in human cells [J].
Lee, NS ;
Dohjima, T ;
Bauer, G ;
Li, HT ;
Li, MJ ;
Ehsani, A ;
Salvaterra, P ;
Rossi, J .
NATURE BIOTECHNOLOGY, 2002, 20 (05) :500-505