Evaluation of cationic liposomes composed of an amino acid-based lipid for neuronal transfection

Nanomedicine. 2010 Feb;6(1):70-7. doi: 10.1016/j.nano.2009.04.005. Epub 2009 May 15.

Abstract

We investigated the ability of cationic liposomes composed of 1,5-dihexadecyl N-arginyl-L-glutamate (Arg-Glu2C(16)) to carry nucleic acids into neuronal cells. Such liposomes have been shown to have a remarkable capacity for transfecting immortalized cell lines. Lipoplexes between the Arg-Glu2C(16) liposomes and plasmid DNA encoding green fluorescent protein (GFP) were analyzed in terms of lipoplex formation, intracellular DNA trafficking, transfection efficiency, and cytotoxicity in neuronal SH-SY5Y cells. A maximum number of cells expressing GFP was obtained with lipoplexes at a lipid-to-DNA ratio of 15. With these lipoplexes, 16% of the cells were GFP-positive, which was approximately fourfold higher than the level obtained with a commercially available transfection reagent, Lipofectamine 2000. Furthermore, as a result of the low cytotoxicity of the Arg-Glu2C(16) lipoplexes, the proportion of GFP-positive cells could be increased to 25% by increasing the concentration of lipoplexes that was applied to the cells. We have demonstrated that Arg-Glu2C(16), as a model cationic amino acid-based lipid, has a high capability as a gene carrier, even for neuronal transfection.

From the clinical editor: In this study, specific cationic liposomes were characterized as nucleic acid transfection agents for neuronal cells. A fourfold higher transfection rate with low cytotoxicity was reported compared to Lipofectamine 2000, a commercial reagent. The authors conclude that the studied cationic liposomes have a high capability as a gene carrier for neuronal transfection. This may become clinically significant in future gene therapy efforts of neuronal diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemistry*
  • Blood Proteins / metabolism
  • Cations
  • Cell Death / drug effects
  • Cell Line, Tumor
  • Chloroquine / pharmacology
  • DNA / metabolism
  • Electrophoretic Mobility Shift Assay
  • Gene Expression Regulation / drug effects
  • Humans
  • Lipids / chemistry*
  • Liposomes / chemistry*
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism*
  • Transfection / methods*

Substances

  • Amino Acids
  • Blood Proteins
  • Cations
  • Lipids
  • Liposomes
  • Chloroquine
  • DNA