Journalartikel

Effects of cell-penetrating peptides and pegylation on transfection efficiency of polyethylenimine in mouse lungs


AutorenlisteNguyen, Juliane; Xie, Xiulan; Neu, Michael; Dumitrascu, Rio; Reul, Regina; Sitterberg, Johannes; Bakowsky, Udo; Schermuly, Ralph; Fink, Ludger; Schmehl, Thomas; Gessler, Tobias; Seeger, Werner; Kissel, Thomas

Jahr der Veröffentlichung2008

Seiten1236-1246

ZeitschriftThe Journal of Gene Medicine

Bandnummer10

Heftnummer11

ISSN1099-498X

DOI Linkhttps://doi.org/10.1002/jgm.1255

VerlagWiley


Abstract

Background Cell-penetrating peptides (CPPs) could potentially be used as vectors for intracellular delivery of proteins, peptides and nucleic acids. The present study examined different CPPs, such as TAT-derived and arginine rich sequences, as well as model amphiphilic peptide, with respect to transfection efficiency of pegylated polyethylenimine (PEI) in A549, Calu-3 cells and in mice after intra-tracheal administration.

Methods The conjugates were prepared by the coupling of CPPs to PEI via a heterobifunctional polyethylene glycol (PEG) linker, resulting in the H-1-bioconjugates CPP-PEG-PEL Structures were successfully confirmed by d nuclear magnetic resonance and diffusion-ordered spectroscopy. Unmodifie PEI 25 kDa was compared with pegylated PEI, and aggregation tendency in cell culture medium, interaction with mucin and stability against heparin was assayed. After evaluating transfection efficiency of the polymers in two different lung cell lines, luciferase reporter gene expression was determined in mouse lungs.

Results All conjugates showed superior transfection efficiency compared to unmodified PEI 25 kDa. The conjugates sizes were generally <300 nm, thus enabling them to penetrate through the mucus lining of the lung and reach the target cells. Coupling of CPPs to PEG-PEI, however, did not significantly improve transfection efficiency in A549 cells, calu-3 cells and in mouse lungs.

Conclusions We show that small and stable polyplex size achieved by pegylation is favourable for successful pulmonary gene delivery. Compared to PEI 25 kDa, pegylated PEI and CPP-PEG-PEI displayed enhanced transfection efficiency both in vitro and in vivo. Copyright (C) 2008 John Wiley & Sons, Ltd.




Zitierstile

Harvard-ZitierstilNguyen, J., Xie, X., Neu, M., Dumitrascu, R., Reul, R., Sitterberg, J., et al. (2008) Effects of cell-penetrating peptides and pegylation on transfection efficiency of polyethylenimine in mouse lungs, The Journal of Gene Medicine, 10(11), pp. 1236-1246. https://doi.org/10.1002/jgm.1255

APA-ZitierstilNguyen, J., Xie, X., Neu, M., Dumitrascu, R., Reul, R., Sitterberg, J., Bakowsky, U., Schermuly, R., Fink, L., Schmehl, T., Gessler, T., Seeger, W., & Kissel, T. (2008). Effects of cell-penetrating peptides and pegylation on transfection efficiency of polyethylenimine in mouse lungs. The Journal of Gene Medicine. 10(11), 1236-1246. https://doi.org/10.1002/jgm.1255



Schlagwörter


cell-penetrating peptidesDOSYGENE DELIVERYHEPARAN-SULFATEHIV-1 TAT PROTEININTRACELLULAR DELIVERYplasmid DNAPOLYETHYLENIMINEpulmonary gene deliveryTRANSDUCTION DOMAIN


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