Poly[Lys-(AEDTP)]: A Cationic Polymer That Allows Dissociation of pDNA/Cationic Polymer Complexes in a Reductive Medium and Enhances Polyfection
- 13 December 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in Bioconjugate Chemistry
- Vol. 13 (1) , 76-82
- https://doi.org/10.1021/bc015503o
Abstract
Polyplexes of high stability resulting from the condensation of a plasmid DNA by a cationic polymer are widely used to develop polymer-based gene delivery systems. However, the plasmid must be released from its vector once inside the cells for an efficient expression of the exogenous gene in the cell nucleus. We have designed a disulfide-containing cationic polymer termed poly[Lys-(AEDTP)] which allowed for the formation of polyplexes and the release of the plasmid in a reductive medium. The amino groups of polylysine were substituted with 3-(2-aminoethyldithio)propionyl residues in order to have each amino group of poly[Lys-(AEDTP)] interacting with a phosphate DNA linked to the polymer backbone via a disulfide bond. As evidenced by agarose gel electrophoresis and ethidium bromide/pDNA fluorescence restoration, poly[Lys-(AEDTP)] polyplexes were decondensed and the plasmid released upon treatment with either dithiothreitol, glutathione in the presence of glutathione reductase, or the thioredoxin reductase. Electron microscopy showed that polyplexes exhibiting spherical particles of a mean size at about 100 nm were decondensed in the presence of glutathione and exhibited filamentous aggregates. Finally, we found that the transfection of 293T7 and HepG2 cells was 10- and 50-fold more efficient with poly[Lys-(AEDTP)] polyplexes, respectively, than with poly[Lys] polyplexes. These results indicate that disulfide-containing cationic polymers must be borne in mind for developping polymer-base gene delivery systems.Keywords
This publication has 9 references indexed in Scilit:
- Reducible cationic lipids for gene transferBiochemical Journal, 2001
- Human Dendritic Cells Transfected with RNA Encoding Prostate-Specific Antigen Stimulate Prostate-Specific CTL Responses In VitroThe Journal of Immunology, 2000
- Size-dependent DNA Mobility in Cytoplasm and NucleusJournal of Biological Chemistry, 2000
- Gene-Delivery Systems Using Cationic PolymersCritical Reviews in Therapeutic Drug Carrier Systems, 1999
- Polylysine-based transfection systems utilizing receptor-mediated deliveryAdvanced Drug Delivery Reviews, 1998
- Interpolyelectrolyte and block ionomer complexes for gene delivery: physico-chemical aspectsAdvanced Drug Delivery Reviews, 1998
- Glycosylated Polylysine/DNA Complexes: Gene Transfer Efficiency in Relation with the Size and the Sugar Substitution Level of Glycosylated Polylysines and with the Plasmid SizeBioconjugate Chemistry, 1995
- Inhibition of leukaemia cell proliferation by folic acid–polylysine-mediated introduction of c-myb antisense oligodeoxynucleotides into HL-60 cellsBritish Journal of Cancer, 1994
- Muramyl dipeptide bound to poly-l-lysine substituted with mannose and gluconoyl residues as macrophage activatorsGlycoconjugate Journal, 1989