Understanding the mechanism of protamine in solid lipid nanoparticle-based lipofection: The importance of the entry pathway

被引:88
作者
Delgado, Diego [1 ]
del Pozo-Rodriguez, Ana [1 ]
Angeles Solinis, Maria [1 ]
Rodriguez-Gascon, Alicia [1 ]
机构
[1] Univ Basque Country UPV EHU, Pharm & Pharmaceut Technol Lab, Fac Pharm, Vitoria 01006, Spain
关键词
Solid lipid nanoparticles; Transfection; Intracellular trafficking; Protamine; Endocytosis; INTRACELLULAR TRAFFICKING; TRANSFECTION EFFICIENCY; CELL TRANSFECTION; GENE-EXPRESSION; LOCALIZATION; LIPOPLEX; DNA; ENHANCEMENT; ENDOCYTOSIS; VECTORS;
D O I
10.1016/j.ejpb.2011.06.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of our study was to evaluate the effect of protamine on the transfection capacity of solid lipid nanoparticles (SLNs) by correlating it to the internalization mechanisms and intracellular trafficking of the vectors. Vectors were prepared with SLN, DNA, and protamine. ARPE-19 and HEK-293 cells were used for the evaluation of the formulations. Protamine induced a 6-fold increase in the transfection of SLNs in retinal cells due to the presence of nuclear localization signals (NLS), its protection capacity, and a shift in the internalization mechanism from caveolae/raft-mediated to clathrin-mediated endocytosis. However, protamine produced an almost complete inhibition of transfection in HEK-293 cells. In spite of the high DNA condensation capacity of protamine and its content in NLS, this does not always lead to an improvement in cell transfection since it may impair some of the limiting steps of the transfection processes. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:495 / 502
页数:8
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