Detalhes do Documento

Human serum albumin enhances DNA transfection by lipoplexes and confers resista...

Autor(es): Simões, Sérgio cv logo 1 ; Slepushkin, Vladimir cv logo 2 ; Pires, Pedro cv logo 3 ; Gaspar, Rogério cv logo 4 ; Pedroso de Lima, Maria C. cv logo 5 ; Düzgünes, Nejat cv logo 6

Data: 2000

Identificador Persistente: http://hdl.handle.net/10316/5812

Origem: Estudo Geral - Universidade de Coimbra

Assunto(s): Gene therapy; Cationic liposome; Human serum albumin; Macrophage; In vivo; Gene delivery


Descrição
Cationic liposome-DNA complexes ([`]lipoplexes') are used as gene delivery vehicles and may overcome some of the limitations of viral vectors for gene therapy applications. The interaction of highly positively charged lipoplexes with biological macromolecules in blood and tissues is one of the drawbacks of this system. We examined whether coating cationic liposomes with human serum albumin (HSA) could generate complexes that maintained transfection activity. The association of HSA with liposomes composed of 1,2-dioleoyl-3-(trimethylammonium) propane and dioleoylphosphatidylethanolamine, and subsequent complexation with the plasmid pCMVluc greatly increased luciferase expression in epithelial and lymphocytic cell lines above that obtained with plain lipoplexes. The percentage of cells transfected also increased by an order of magnitude. The zeta potential of the ternary complexes was lower than that of the lipoplexes. Transfection activity by HSA-lipoplexes was not inhibited by up to 30% serum. The combined use of HSA and a pH-sensitive peptide resulted in significant gene expression in human primary macrophages. HSA-lipoplexes mediated significantly higher gene expression than plain lipoplexes or naked DNA in the lungs and spleen of mice. Our results indicate that negatively charged HSA-lipoplexes can facilitate efficient transfection of cultured cells, and that they may overcome some of the problems associated with the use of highly positively charged complexes for gene delivery in vivo. http://www.sciencedirect.com/science/article/B6T1T-3YJ9DWD-V/1/9ba1203dc49f64eb459d6785098bd10a
Tipo de Documento Artigo
Idioma Inglês
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