Factors mediating lipofection potency of a series of cationic phosphonolipids in human cell lines

被引:14
作者
Koumbi, Daphne
Clement, Jean-Claude
Sideratou, Zili
Yaouanc, Jean-Jacques
Loukopoulos, Dimitris
Kollia, Panagoula [1 ]
机构
[1] Univ Thessaloniki, Lab Mol Genet & Cytogenet, Sch Med, Larisa, Greece
[2] Univ Athens, Dept Med 1, Sch Med, Athens, Greece
[3] UBO, Lab Chim Organ, CNRS, UMR 6521, Brest, France
[4] NCSR, DEMOKRITOS, Inst Phys Chem, Athens, Greece
[5] Acad Athens, Fdn Biomed Res, Athens, Greece
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2006年 / 1760卷 / 08期
关键词
cationic phosphonolipid; lipofection condition; gene transfer; transgene expression; nuclear DNA incorporation;
D O I
10.1016/j.bbagen.2006.03.005
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
A series of cationic liposomes known as cationic phosphonolipids (CPs) were evaluated as vehicles for in vitro gene transfer in K562 erythroleukemia cells and 5637 epithelial carcinoma cells. For each CP and target cell type examined, detailed analyses were performed to determine optimal transfection conditions (lipid/DNA (+/-) charge ratio, amount of complexed episomal DNA. liposomal and lipoplex size. complexation medium and duration of complex-cell exposure time). Lipofection conditions were determined to be both cell- and lipid-type specific. Complexation medium critically affected transfection competence. The initial size of the liposome was not always predictive of lipofection potency. The lipid chemical composition had a strong impact upon lipofection efficiency: DOPE inclusion in the liposome formulations was found to affect the levels of transgene expression in a cell-dependent way. Notably. effective transgene expression was characterized by prominent plasmid noclear incorporation. Human A gamma- and epsilon-globin transgene nuclear incorporation and expression in 5637 cells post GLB.391-mediated lipofection lends credence to its use as a vehicle of therapeutic transgene delivery. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1151 / 1159
页数:9
相关论文
共 47 条
[1]   INDUCTION OF ERYTHROID-DIFFERENTIATION IN THE HUMAN LEUKEMIA CELL-LINE K562 [J].
ANDERSSON, LC ;
JOKINEN, M ;
GAHMBERG, CG .
NATURE, 1979, 278 (5702) :364-365
[2]   EFFICIENT GENE-TRANSFER INTO MAMMALIAN PRIMARY ENDOCRINE-CELLS WITH LIPOPOLYAMINE-COATED DNA [J].
BEHR, JP ;
DEMENEIX, B ;
LOEFFLER, JP ;
MUTUL, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (18) :6982-6986
[3]  
CAPPECHI MR, 1980, CELL, V22, P479
[4]  
Castelli P, 2005, J ENDOVASC THER, V12, P8
[5]  
da Cruz MTG, 2001, BBA-BIOMEMBRANES, V1510, P136
[6]   Biodistribution study of phosphonolipids:: a class of non-viral vectors efficient in mice lung-directed gene transfer [J].
Delépine, P ;
Guillaume, C ;
Montier, T ;
Clément, JC ;
Yaouanc, JJ ;
Abbayes, HD ;
Berthou, F ;
Le Pape, A ;
Férec, C .
JOURNAL OF GENE MEDICINE, 2003, 5 (07) :600-608
[7]  
Delépine P, 2000, J PHARM SCI, V89, P629
[8]   Biophysical characterization of cationic lipid:DNA complexes [J].
Eastman, SJ ;
Siegel, C ;
Tousignant, J ;
Smith, AE ;
Cheng, SH ;
Scheule, RK .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1997, 1325 (01) :41-62
[9]  
FELGNER JH, 1994, J BIOL CHEM, V269, P2550
[10]   Improved cationic lipid formulations for in vivo gene therapy [J].
Felgner, PL ;
Tsai, YJ ;
Sukhu, L ;
Wheeler, CJ ;
Manthorpe, M ;
Marshall, J ;
Cheng, SH .
DNA VACCINES: A NEW ERA IN VACCINOLOGY, 1995, 772 :126-139