Self-Assembly of Ternary Insulin-Polyethylenimine (PEI)-DNA Nanoparticles for Enhanced Gene Delivery and Expression in Alveolar Epithelial Cells

被引:43
作者
Elfinger, Markus [1 ,2 ]
Pfeifer, Corinna [1 ,2 ]
Uezguen, Senta [1 ,2 ]
Golas, Monika M. [3 ]
Sander, Bjoern [3 ]
Maucksch, Christof [1 ,2 ]
Stark, Holger [3 ]
Aneja, Manish K. [1 ]
Rudolph, Carsten [1 ,2 ]
机构
[1] Univ Munich, Dept Pediat, D-80337 Munich, Germany
[2] Free Univ Berlin, Dept Pharm, D-14166 Berlin, Germany
[3] Max Planck Inst Biophys Chem, Dimens Electron Cryomicroscopy Grp 3, D-37077 Gottingen, Germany
关键词
ELECTRON-MICROSCOPY; IN-VIVO; OLIGONUCLEOTIDE; TRANSLOCATION; RECEPTORS; THERAPY; NUCLEI; VECTOR;
D O I
10.1021/bm900707j
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Enhancing gene delivery and expression in alveolar epithelial cells could offer the opportunity for the treatment of acquired and inherited lung diseases. Here, we show that particle adsorption of human insulin (INS) is capable of increasing plasmid DNA (pDNA) delivery from polyethylenimine (PEI) nanoparticles specifically in alveolar epithelial cells. INS receptors were predominantly detected on alveolar but not on bronchial epithelial cells. INS was adsorbed on the surface of PEI gene vectors by spontaneous self-assembly resulting in ternary PEI-pDNA-INS nanoparticles. Surface adsorption was confirmed by particle size, surface charge, and fluorescence resonance energy transfer (FRET) measurements. INS adsorption significantly increased gene expression of PEI-pDNA nanoparticles up to 16-fold on alveolar epithelial cells but not on bronchial epithelia] cells. This increased gene expression was INS receptor specific. Our results demonstrate that targeting INS receptor for gene delivery in alveolar epithelial cells represents a promising approach for enhanced gene delivery and expression.
引用
收藏
页码:2912 / 2920
页数:9
相关论文
共 24 条
[1]   CRYO-ELECTRON MICROSCOPY OF VIRUSES [J].
ADRIAN, M ;
DUBOCHET, J ;
LEPAULT, J ;
MCDOWALL, AW .
NATURE, 1984, 308 (5954) :32-36
[2]   Different strategies for formation of PEGylated EGF-conjugated PEI/DNA complexes for targeted gene delivery [J].
Blessing, T ;
Kursa, M ;
Holzhauser, R ;
Kircheis, R ;
Wagner, E .
BIOCONJUGATE CHEMISTRY, 2001, 12 (04) :529-537
[3]   A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE [J].
BOUSSIF, O ;
LEZOUALCH, F ;
ZANTA, MA ;
MERGNY, MD ;
SCHERMAN, D ;
DEMENEIX, B ;
BEHR, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7297-7301
[4]   Characterization of lactoferrin as a targeting ligand for nonviral gene delivery to airway epithelial cells [J].
Elfinger, Markus ;
Maucksch, Christof ;
Rudolph, Carsten .
BIOMATERIALS, 2007, 28 (23) :3448-3455
[5]  
Guo WJ, 1999, AAPS PHARMSCI, V1
[6]   Mechanisms of nuclear translocation of insulin [J].
Harada, S ;
Smith, RM ;
Jarett, L .
CELL BIOCHEMISTRY AND BIOPHYSICS, 1999, 31 (03) :307-319
[7]   Interaction of polycationic polymers with supported lipid bilayers and cells: Nanoscale hole formation and enhanced membrane permeability [J].
Hong, Seungpyo ;
Leroueil, Pascale R. ;
Janus, Elizabeth K. ;
Peters, Jennifer L. ;
Kober, Mary-Margaret ;
Islam, Mohammad T. ;
Orr, Bradford G. ;
Baker, James R., Jr. ;
Holl, Mark M. Banaszak .
BIOCONJUGATE CHEMISTRY, 2006, 17 (03) :728-734
[8]   Evaluation by fluorescence resonance energy transfer of the stability of nonviral gene delivery vectors under physiological conditions [J].
Itaka, K ;
Harada, A ;
Nakamura, K ;
Kawaguchi, H ;
Kataoka, K .
BIOMACROMOLECULES, 2002, 3 (04) :841-845
[9]   Coupling of cell-binding ligands to polyethylenimine for targeted gene delivery [J].
Kircheis, R ;
Kichler, A ;
Wallner, G ;
Kursa, M ;
Ogris, M ;
Felzmann, T ;
Buchberger, M ;
Wagner, E .
GENE THERAPY, 1997, 4 (05) :409-418
[10]   A model for non-viral gene delivery: through syndecan adhesion molecules and powered by actin [J].
Kopatz, I ;
Remy, JS ;
Behr, JP .
JOURNAL OF GENE MEDICINE, 2004, 6 (07) :769-776