Background: Cationic polymers and liposomes are used to wrap DNA into complexes that promote its cellular uptake. The mechanisms of the uptake and the intracellular fate of these complexes are obscure, as are reasons for an unpredictable and sometimes poor efficiency of the transgene expression. Polyanionic glycosaminoglycans (GAGs) on the cell surface interact with the cationic DNA complexes and influence transfection.
Methods: The quantities of heparan sulfate (HS), chondroitin sulfate (CS) and hyaluronan (HA) on the cell surface of mutated Chinese hamster ovary (CHO) cells and manipulated (chlorate, xyloside, chondroitinase ABC or Streptomyces hyaluronidase) smooth muscle cells were correlated with the uptake of four different DNA complexes, and the expression of the transgene.
Results: Two CHO mutants, without cell-surface HS and CS, showed a 1.5-6-fold increase in cellular association of DNA, and 3-25-fold increase of transgene expression, as compared with the wild type. A CHO mutant with a 5.7-fold increase of cell-surface CS, but devoid of HS, showed enhanced DNA association, but 20-40% reduction in its expression. The removal of HS, CS, or HA from the cell surface of smooth muscle cells had a minor or insignificant effect on the cell association and transfection of the carriers and only polyethyleneimine showed increased association and expression of the transgene.
Conclusions: The uptake of DNA complexes varies depending on carrier, cell type and amounts of cell-surface HS, CS, and HA, whereas all GAGs inhibit the transgene expression. This implies that cell-surface GAGs probably direct complexes into intracellular compartments that do not support transcription.
Copyright 2004 John Wiley & Sons, Ltd.