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• W2063668324 abstract "Cell transfection requires cationic DNA complexes and heparan sulfate proteoglycans (HSPGs) at the cell surface. Syndecans are transmembrane HSPGs that are ubiquitously expressed on adherent cells. Their polyanionic heparan sulfate moieties are bound at the distal end of their ectodomain, thus facilitating interaction with large cationic particles.We propose a model for cell entry involving syndecans as receptors for the DNA complexes by comparing transfection with bacteria uptake and using drug inhibition experiments along with confocal microscopy.When combined with results from the literature, our data suggest the following sequence of events: after initial particle binding, gradual electrostatic zippering of the plasma membrane onto the particle is sustained by lateral diffusion of syndecan molecules that cluster into cholesterol-rich rafts. Clustering in turn triggers PKC activity and linker protein-mediated actin binding to the cytoplasmic tail of the syndecans. Resulting tension fibers and a growing network of cortical actin may then pull the particle into the cell.Diversion of integrin- and syndecan-mediated cell adhesion processes for particle engulfment appears to be widely exploited by animals (chylomicrons), by pathogens (bacteria, viruses) and, as suggested here, by non-viral vectors." @default.
• W2063668324 created "2016-06-24" @default.
• W2063668324 creator A5036662114 @default.
• W2063668324 creator A5056478667 @default.
• W2063668324 creator A5087483456 @default.
• W2063668324 date "2004-03-10" @default.
• W2063668324 modified "2023-10-18" @default.
• W2063668324 title "A model for non-viral gene delivery: through syndecan adhesion molecules and powered by actin" @default.
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• W2063668324 doi "https://doi.org/10.1002/jgm.558" @default.
• W2063668324 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15241784" @default.
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