Transient gene expression in mammalian cells grown in serum-free suspension culture

被引:86
作者
Schlaeger, EJ [1 ]
Christensen, K [1 ]
机构
[1] F Hoffmann La Roche & Co Ltd, Res Labs, CH-4070 Basel, Switzerland
关键词
gene expression; HEK293(EBNA) cells; serum-free; transient transfection;
D O I
10.1023/A:1008000327766
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In order to establish a simple and scaleable transfection system we have used the cationic polymer polyethylenimine (PEI) to study transient transfection in HEK293 and 293 (EBNA) cells grown in serum-free suspension culture. The transfection complexes were made directly within the cell culture by consecutively adding plasmid and PEI (direct method). Alternatively, the DNA-PEI transfection complexes were prepared in fresh medium (1/10 culture volume) and then added to the cells (indirect method). The results of this study clearly show that the ratio of PEI nitrogen to DNA phosphate is very important for high expression levels. The precise ratio is dependent on the DNA concentration. For example, using 1 mu g/ml DNA by the indirect method, the ratio of optimal PEI:DNA was about 10-13:1. However, the ratio increases to 33:1 for 0.1-0.2 mu g/ ml DNA. By testing several different molecular weights of the polycationic polymer we could show that the highest transfection efficiency was obtained with the PEI 25 kDa. Using PEI 25 kDa the indirect method is superior to the direct addition because significantly lower DNA concentrations are needed. The expression levels of the soluble human TNF receptor p55 are even higher at low DNA compared to 1 mu g/ml plasmid. The EBV-based pREP vectors gave better transient gene expression when used in 293( EBNA) cells compared to HEK293 cells in suspension culture. No differences in expression levels in the two cell lines were observed when the pC1 (CMV)-TNFR was used. In conclusion, PEI is a low-toxic transfection agent which provides high levels of transient gene expression in 293(EBNA) cells grown in serum-free suspension culture. This system allows highly reproducible, cost-effective production of milligram amounts of recombinant proteins in 2-5 l spinner culture scale within 3-5 days. Fermentor scale experiments, however, are less efficient because the PEI-mediated transient tranfection is inhibited by conditioned medium.
引用
收藏
页码:71 / 83
页数:13
相关论文
共 27 条
[1]   Polyethylenimine (PEI) is a simple, inexpensive and effective reagent for condensing and linking plasmid DNA to adenovirus for gene delivery [J].
Baker, A ;
Saltik, M ;
Lehrmann, H ;
Killisch, I ;
Mautner, V ;
Lamm, G ;
Christofori, G ;
Cotten, M .
GENE THERAPY, 1997, 4 (08) :773-782
[2]   GENE-TRANSFER OPTIMIZATION WITH LIPOSPERMINE-COATED DNA [J].
BARTHEL, F ;
REMY, JS ;
LOEFFLER, JP ;
BEHR, JP .
DNA AND CELL BIOLOGY, 1993, 12 (06) :553-560
[3]  
BIRNBOIM HC, 1983, METHOD ENZYMOL, V100, P243
[4]   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
[5]  
Boussif O, 1996, GENE THER, V3, P1074
[6]  
BRASIER AR, 1989, BIOTECHNIQUES, V7, P1116
[7]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[8]  
Gao X, 1995, GENE THER, V2, P710
[9]   SCALE-UP OF THE ADENOVIRUS EXPRESSION SYSTEM FOR THE PRODUCTION OF RECOMBINANT PROTEIN IN HUMAN 293S CELLS [J].
GARNIER, A ;
COTE, J ;
NADEAU, I ;
KAMEN, A ;
MASSIE, B .
CYTOTECHNOLOGY, 1994, 15 (1-3) :145-155
[10]   SOLUBLE RECEPTORS FOR TUMOR-NECROSIS-FACTOR AS PREDICTORS OF PROGRESSION TO AIDS IN ASYMPTOMATIC HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION [J].
GODFRIED, MH ;
VANDERPOLL, T ;
WEVERLING, GJ ;
MULDER, JW ;
JANSEN, J ;
VANDEVENTER, SJH ;
SAUERWEIN, HP .
JOURNAL OF INFECTIOUS DISEASES, 1994, 169 (04) :739-745