Effect of electric field vectoriality on electrically mediated gene delivery in mammalian cells

被引:70
作者
Faurie, C [1 ]
Phez, E [1 ]
Golzio, M [1 ]
Vossen, C [1 ]
Lesbordes, JC [1 ]
Delteil, C [1 ]
Teissié, J [1 ]
Rols, MP [1 ]
机构
[1] CNRS, UMR 5089, Inst Pharmacol & Biol Struct, F-31077 Toulouse, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2004年 / 1665卷 / 1-2期
关键词
electric field; electroporation; permeabilization; gene transfer; videomicroscopy;
D O I
10.1016/j.bbamem.2004.06.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Electropermeabilization is a nonviral method used to transfer genes into living cells. Up to now, the mechanism is still to be elucidated. Since cell permeabilization, a prerequired for gene transfection, is triggerred by electric field, its characteristics should depend on its vectorial properties. The present investigation addresses the effect of pulse polarity and orientation on membrane permeabilization and gene delivery by electric pulses applied to cultured mammalian cells. This has been directly observed at the single-cell level by using digitized fluorescence microscopy. While cell permeabilization is only slightly affected by reversing the polarity of the electric pulses or by changing the orientation of pulses, transfection level increases are observed. These last effects are due to an increase in the cell membrane area where DNA interacts. Fluorescently labelled plasmids only interact with the electropermeabilized side of the cell facing the cathode. The plasmid interaction with the electropermeabilized cell surface is stable and is not affected by pulses of reversed polarities. Under such conditions, DNA interacts with the two sites of the cell facing the two electrodes. When changing both the pulse polarity and their direction, DNA interacts with the whole membrane cell surface. This is associated with a huge increase in gene expression. This present study demonstrates the relationship between the DNA/membrane surface interaction and the gene transfer efficiency, and it allows to define the experimental conditions to optimize the yield of transfection of mammalian cells. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:92 / 100
页数:9
相关论文
共 43 条
[1]
Gene transfer into muscle by electroporation in vivo [J].
Aihara, H ;
Miyazaki, J .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :867-870
[2]
Passive entry of a DNA molecule into a small pore [J].
de Gennes, PG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (13) :7262-7264
[3]
Cell and animal imaging of electrically mediated gene transfer [J].
Faurie, C ;
Golzio, M ;
Moller, P ;
Teissié, J ;
Rols, MP .
DNA AND CELL BIOLOGY, 2003, 22 (12) :777-783
[4]
Time courses of mammalian cell electropermeabilization observed by millisecond imaging of membrane property changes during the pulse [J].
Gabriel, B ;
Teissié, J .
BIOPHYSICAL JOURNAL, 1999, 76 (04) :2158-2165
[5]
Direct observation in the millisecond time range of fluorescent molecule asymmetrical interaction with the electropermeabilized cell membrane [J].
Gabriel, B ;
Teissie, J .
BIOPHYSICAL JOURNAL, 1997, 73 (05) :2630-2637
[6]
GABRIEL B, 1995, EUR J BIOCHEM, V228, P708
[7]
Analytical description of the transmembrane voltage induced on arbitrarily oriented ellipsoidal and cylindrical cells [J].
Gimsa, J ;
Wachner, D .
BIOPHYSICAL JOURNAL, 2001, 81 (04) :1888-1896
[8]
Direct visualization at the single-cell level of electrically mediated gene delivery [J].
Golzio, M ;
Teissié, J ;
Rols, MP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (03) :1292-1297
[9]
In vivo gene electroinjection and expression in rat liver [J].
Heller, R ;
Jaroszeski, M ;
Atkin, A ;
Moradpour, D ;
Gilbert, R ;
Wands, J ;
Nicolau, C .
FEBS LETTERS, 1996, 389 (03) :225-228
[10]
TIME COURSES OF CELL ELECTROPORATION AS REVEALED BY SUBMICROSECOND IMAGING OF TRANSMEMBRANE POTENTIAL [J].
HIBINO, M ;
ITOH, H ;
KINOSITA, K .
BIOPHYSICAL JOURNAL, 1993, 64 (06) :1789-1800