Disassembly of polyethylenimine-DNA particles in vitro: Implications for polyethylenimine-mediated DNA delivery

被引:98
作者
Bertschinger, Martin [1 ]
Backliwal, Gaurav [1 ]
Schertenleib, Arnaud [1 ]
Jordan, Martin [1 ]
Hacker, David L. [1 ]
Wurm, Florian M. [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Lab Cellular Biotechnol, CH-1015 Lausanne, Switzerland
关键词
DNA transfection; polyethylenimine; plasmid DNA; nanoparticles; mammalian cells;
D O I
10.1016/j.jconrel.2006.09.006
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Here a simple in vitro assay was used to investigate the disassembly of nanoparticles of polyethylenimine (PEI) and DNA. Particles were formed with various PEN, allowed to mature for 10 min, and then exposed to different competitors (RNA, DNA, BSA or heparin) or to different conditions of pH or osmolarity. DNA release was determined by gel electrophoresis or spectroscopy. The presence of heparin or high salt yielded complete particle disassembly for all PEIs tested. The addition of RNA to particles formed with linear PEIs or branched 2 kDa PEI resulted in rapid DNA release, but RNA induced only partial disassembly of particles formed with large branched PEIs. In the presence of competitor DNA, slow disassembly was observed with particles made with linear PEIs or branched 2 kDa PEI but not for particles made with larger branched PEIs. The presence of BSA resulted in partial disassembly of PEI-DNA particles, but acidic pH did not affect particle stability. If particles were allowed to mature longer than 10 min in NaCl, subsequent heparin-mediated DNA release decreased as the incubation time and the PEI:DNA ratio increased. However, particles that matured in culture medium were disassembled by heparin independently of maturation time or PEI:DNA ratio. It was concluded that branched PEIs have a higher affinity for DNA than linear PEIs, that the intracellular disassembly of PEI-DNA particles may involve interactions between PEI and cellular RNA, and that extended maturation of PEI-DNA particles in NaCl prior to transfection may limit the intracellular release of plasmid DNA. (c) 2006 Published by Elsevier B.V.
引用
收藏
页码:96 / 104
页数:9
相关论文
共 32 条
[1]   A spectrophotometric assay for the quantification of polyethylenimine in DNA nanoparticles [J].
Bertschinger, M ;
Chaboche, S ;
Jordan, M ;
Wurm, FM .
ANALYTICAL BIOCHEMISTRY, 2004, 334 (01) :196-198
[2]   Intracellular route and transcriptional competence of polyethylenimine-DNA complexes [J].
Bieber, T ;
Meissner, W ;
Kostin, S ;
Niemann, A ;
Elsasser, HP .
JOURNAL OF CONTROLLED RELEASE, 2002, 82 (2-3) :441-454
[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]   Intracellular dynamics of the gene delivery vehicle polyethylenimine during transfection:: investigation by two-photon fluorescence correlation spectroscopy [J].
Clamme, JP ;
Krishnamoorthy, G ;
Mély, Y .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1617 (1-2) :52-61
[5]   In vivo delivery to tumors of DNA complexed with linear polyethylenimine [J].
Coll, JL ;
Chollet, P ;
Brambilla, E ;
Desplanques, D ;
Behr, JP ;
Favrot, M .
HUMAN GENE THERAPY, 1999, 10 (10) :1659-1666
[6]   Factors affecting blood clearance and in vivo distribution of polyelectrolyte complexes for gene delivery [J].
Dash, PR ;
Read, ML ;
Barrett, LB ;
Wolfert, M ;
Seymour, LW .
GENE THERAPY, 1999, 6 (04) :643-650
[7]   Serum-free large-scale transient transfection of CHO cells [J].
Derouazi, M ;
Girard, P ;
Van Tilborgh, F ;
Iglesias, K ;
Muller, N ;
Bertschinger, M ;
Wurm, FM .
BIOTECHNOLOGY AND BIOENGINEERING, 2004, 87 (04) :537-545
[8]   Nanoscopic structure of DNA condensed for gene delivery [J].
Dunlap, DD ;
Maggi, A ;
Soria, MR ;
Monaco, L .
NUCLEIC ACIDS RESEARCH, 1997, 25 (15) :3095-3101
[9]  
Godbey WT, 2000, J BIOMED MATER RES, V51, P321, DOI 10.1002/1097-4636(20000905)51:3<321::AID-JBM5>3.0.CO
[10]  
2-R