Cationic and anionic lipoplexes inhibit gene transfection by electroporation in vivo

J Gene Med. 2010 Jun;12(6):491-500. doi: 10.1002/jgm.1460.

Abstract

Background: Nonviral gene therapy still suffers from low efficiency. Methods that would lead to higher gene expression level of longer duration would be a major advance in this field. Lipidic vectors and physical methods have been investigated separately, and both induced gene expression improvement.

Methods: We sought to combine both chemical and physical methods. Cationic or anionic lipids can potentially destabilize the cell membrane and could consequently enhance gene delivery by a physical method such as electrotransfer. A plasmid model encoding luciferase was used, either free or associated with differently-charged lipoplexes before electrotransfer.

Results: Electrotransfer alone strongly enhanced gene expression after intramuscular and intradermal injection of naked DNA. On the other hand, cationic and anionic lipoplex formulations decreased gene expression after electrotransfer, whereas poorly-charged thiourea-based complexes, brought no benefit. Pre-injection of the lipids, followed by administration of naked DNA, did not modified gene expression induced by electroporation in the skin.

Conclusions: The results obtained in the present study suggest that packing of DNA plasmid in lipoplexes strongly decreases the efficiency of gene electrotransfer, independently of the lipoplex charge. Non-aggregating complexes, such as poorly-charged thiourea-based complexes, should be preferred to increase DNA release.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Cations / chemistry*
  • Cations / metabolism
  • Cricetinae
  • Cricetulus
  • DNA / chemistry
  • Electroporation / methods*
  • Female
  • Gene Transfer Techniques*
  • Liposomes / chemistry*
  • Liposomes / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Muscle, Skeletal / cytology
  • Muscle, Skeletal / physiology
  • Plasmids / chemistry
  • Plasmids / genetics
  • Skin / cytology
  • Skin / metabolism
  • Transfection*

Substances

  • Cations
  • Liposomes
  • DNA