Efficient gene transfer into mammalian cells using fusogenic liposome

Biochem Biophys Res Commun. 1996 Jan 5;218(1):402-7. doi: 10.1006/bbrc.1996.0070.

Abstract

Fusogenic liposome (FL) based on Sendai virus constitutes a unique system that delivers the content efficiently into animal cells in vitro and in vivo. In this study we characterized unilamellar FL as a gene transfer vector in comparison with cationic lipid (CL)-DNA complex. FL transferred genes efficiently into cultured cells even when incubated for as little as 10 min, while CL-DNA complex required at least 30 min to reach the same level of gene expression. FL was also much less cytotoxic than CL-DNA complex under the conditions that resulted in the same level of gene expression. In addition, FL maintained 70% of the transfection activity even in the presence of 40% fetal calf serum (FCS), while CL-DNA complex almost completely lost their activity in the presence of 5% FCS. Furthermore, we found that FL could introduce and express luciferase gene into mouse ascites tumor cells in vivo, but CL-DNA complex could not even at higher concentrations of DNA. We conclude that unilamellar FL is a unique and efficient nonviral vector for gene transfer in vitro and in vivo.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / genetics
  • Animals
  • Base Sequence
  • Cell Survival
  • Cells, Cultured
  • Chickens
  • Gene Transfer Techniques*
  • Genes, Viral
  • Liposomes
  • Luciferases / analysis
  • Luciferases / biosynthesis
  • Male
  • Mammals
  • Membrane Fusion
  • Mice
  • Mice, Inbred Strains
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Oligodeoxyribonucleotides
  • Parainfluenza Virus 1, Human*
  • Recombinant Proteins / analysis
  • Recombinant Proteins / biosynthesis*
  • Restriction Mapping
  • Sarcoma, Experimental* / pathology
  • Transfection / methods*

Substances

  • Actins
  • Liposomes
  • Oligodeoxyribonucleotides
  • Recombinant Proteins
  • Luciferases