Insights in cellular uptake mechanisms of pDNA–polycationic amphiphilic cyclodextrin nanoparticles (CDplexes)

8 páginas, 7 figuras, 2 esquemas.It is generally recognized that the major obstacle to efficient gene delivery is cellular internalization and endosomal escape of the DNA. Recently, we have developed a modular strategy for the preparation of well-defined polycationic amphiphilic cyclodextrins (paCDs) capable of complexing and compacting DNA into homogeneous nanoparticles (< 70 nm). Since paCDs resemble both cationic polymers and cationic lipids, it is conceivable that the corresponding pDNA–paCD nanoparticles (CDplexes) might use the cell internalization and endosomal escape mechanisms described for both lipoplexes and polyplexes. To verify this hypothesis, we have now investigated the uptake and transfection efficiencies of CDplexes in the presence of several inhibitors of endocytosis, namely chlorpromazine, genistein, dynasore and methylated β-cyclodextrin (MbCD). Our data show that CDplexes obtained from paCD 1, which ranks among the most efficient paCD gene vectors reported up to date, are internalized by both clathrin-dependent (CDE) and clathrin-independent endocytosis (CIE), both processes being cholesterol- and dynamin-dependent. We observed that the largest fraction of gene complexes is taken up via CDE, but this fraction is less relevant for transfection. The smaller fraction that is internalized via the CIE pathway is predominantly responsible for successful transfection.This work was supported by the Spanish Ministerio de Innovación y Ciencia (MICINN, contract numbers CTQ2006-15515-C02-01/BQU and CTQ2007-61180/PPQ) and the Junta de Andalucía (P06-FQM-01601 and P07-FQM-2774). ADM is grateful to the CSIC for a pre-doctoral fellowship. DV is a doctoral fellow of the Institute for the Promotion of Innovation through Science and Technology in Flanders (IWT), Belgium. We gratefully acknowledge the European Commission for funding through the Integrated 6th Framework Programme MediTrans and the Lab of Pharmaceutical Biotechnology (Ghent University) of Prof. D. Deforce for the access to their flow cytometer.Peer reviewe