Effect of vinblastine on transfection: Influence of cell types, cationic lipids and promoters

Li Wang*, David A. Dean, Robert C. MacDonald

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

As previously shown, vinblastine, when incorporated into a cationic lipid prior to generation of lipoplexes, increases by ∼30-fold the extent of transfection of pβ-Gal with a cytomegalovirus promoter (pCMV-β-Gal) to vascular smooth muscle cells (VSMC) by 1,2-dioleoyl-sn-glycero-3- ethylphosphocholine (EDOPC)-pCMV-β-Gal complexes. To test if this increase is limited to VSMC and EDOPC, or is general, we examined three other cell types, human umbilical artery endothelial cells (HUAEC), baby hamster kidney (BHK) cells and 293 cells derived from human kidney, as well as a different cationic lipid, 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP). In addition, to determine the contribution of the NF-κB transcription factor to the vinblastine effect, pCMV was replaced with a smooth muscle γ-actin gene promoter, SMGA, which, unlike pCMV, does not respond to NF-κB. It was found that on all cell types we tested, the transfection efficiency increased with vinblastine incorporation; however, the magnitude depended greatly on the cell type, e.g. whereas the transfection of VSMC increased ∼30-fold, that of 293 cells increased only ∼2-fold. The cationic phospholipid could be replaced with DOTAP with no loss of effect. In contrast, the promoter was critical and the stimulation was lost if pCMV was replaced with pSMGA. It is concluded that the positive effect of vinblastine on transfection is general and the stimulation of the transcription factor NF-κB is involved in this action. The activation of NF-κB by anti-microtubule agents should thus allow for transfection of specific cell types by vinblastine lipoplexes.

Original languageEnglish (US)
Pages (from-to)93-96
Number of pages4
JournalCurrent Drug Delivery
Volume2
Issue number1
DOIs
StatePublished - Jan 2005

Keywords

  • Intracellular transport
  • NF-κB
  • Smooth muscle γ-actin gene promoter
  • Transfection
  • Vinblastine

ASJC Scopus subject areas

  • Pharmaceutical Science

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