The influence of alkyl pyridinium sponge toxins on membrane properties, cytotoxicity, transfection and protein expression in mammalian cells

Biochim Biophys Acta. 2003 Aug 7;1614(2):171-81. doi: 10.1016/s0005-2736(03)00175-5.

Abstract

The ability of two alkyl pyridinium sponge toxin preparations (poly-APS and halitoxin) to form transient pores/lesions in cell membranes and allow transfection of plasmid cDNA have been investigated using HEK 293 cells. Poly-APS and halitoxin preparations caused a collapse in membrane potential, reductions in input resistance and increased Ca2+ permeability. At least partial recovery was observed after poly-APS application but recovery was more rarely seen with halitoxin. The transfection with plasmid cDNAs for an enhanced green fluorescent protein (EGFP) and human tumour necrosis factor receptor 2 (TNFR2) was assessed for both toxin preparations and compared with lipofectamine. Stable transfection was achieved with poly-APS although it was less efficient than lipofectamine. These results show that viable cells transfected with alien cDNA can be obtained using novel transient pore-forming alkyl pyridinium sponge toxins and a simple pre-incubation protocol. This provides the first proof of principle that pore-forming alkyl pyridinium compounds can be used to deliver cDNA to the intracellular environment without permanently compromising the plasma membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / biosynthesis
  • Antigens, CD / genetics
  • Cell Line
  • Cell Membrane / drug effects*
  • Cell Membrane / metabolism
  • DNA, Complementary / metabolism
  • Endocytosis
  • Green Fluorescent Proteins
  • Humans
  • Lipids
  • Luminescent Proteins / biosynthesis
  • Luminescent Proteins / genetics
  • Marine Toxins / pharmacology*
  • Membrane Potentials / drug effects
  • Microscopy, Confocal
  • Plasmids
  • Polymers / pharmacology*
  • Porifera*
  • Protein Biosynthesis*
  • Proteins / genetics
  • Pyridinium Compounds / pharmacology*
  • Receptors, Tumor Necrosis Factor / biosynthesis
  • Receptors, Tumor Necrosis Factor / genetics
  • Receptors, Tumor Necrosis Factor, Type II
  • Transfection / methods

Substances

  • Antigens, CD
  • DNA, Complementary
  • Lipids
  • Lipofectamine
  • Luminescent Proteins
  • Marine Toxins
  • Polymers
  • Proteins
  • Pyridinium Compounds
  • Receptors, Tumor Necrosis Factor
  • Receptors, Tumor Necrosis Factor, Type II
  • halitoxin
  • poly-APS
  • Green Fluorescent Proteins