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

被引:2
|
作者
Ernst-Jürgen Schlaeger
Klaus Christensen
机构
[1] F. Hoffmann La Roche Ltd.,Research Laboratories
来源
Cytotechnology | 1999年 / 30卷
关键词
gene expression; HEK293(EBNA) cells; serum-free; transient transfection;
D O I
暂无
中图分类号
学科分类号
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 μg/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 μg/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 μg/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
下载
收藏
页码:71 / 83
页数:12
相关论文
共 50 条
  • [21] Calcium phosphate transfection optimization for serum-free suspension culture
    Girard, P
    Porte, L
    Berta, T
    Jordan, M
    Wurm, FM
    CYTOTECHNOLOGY, 2001, 35 (03) : 175 - 180
  • [22] Adhesion of suspension cells on a coverslip in serum-free conditions
    Nakayama, Tomofumi
    Mihara, Keiko
    Kawata, Jin
    Kimura, Hiroshi
    Saitoh, Hisato
    ANALYTICAL BIOCHEMISTRY, 2014, 466 : 1 - 3
  • [23] Fetal calf serum-free suspension culture of Chinese hamster ovary cells employing fish serum
    Fujiwara, Masashi
    Aizu, Yu
    Shioya, Itaru
    Takagi, Mutsumi
    JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2010, 109 (03) : 307 - 309
  • [24] Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII
    Swiech, Kamilla
    Kamen, Amine
    Ansorge, Sven
    Durocher, Yves
    Picanco-Castro, Virginia
    Russo-Carbolante, Elisa M. S.
    Neto, Mario S. A.
    Covas, Dimas T.
    BMC BIOTECHNOLOGY, 2011, 11
  • [25] Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII
    Kamilla Swiech
    Amine Kamen
    Sven Ansorge
    Yves Durocher
    Virgínia Picanço-Castro
    Elisa MS Russo-Carbolante
    Mário SA Neto
    Dimas T Covas
    BMC Biotechnology, 11
  • [26] A serum-free and defined medium for the culture of mammalian postimplantation embryos
    Drakou, Katerina
    Georgiades, Pantelis
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2015, 468 (04) : 813 - 819
  • [27] Serum-free suspension large-scale transient transfection of CHO cells in WAVE bioreactors
    Haldankar, Raj
    Li, Danqing
    Saremi, Zane
    Baikalov, Claudia
    Deshpande, Rohini
    MOLECULAR BIOTECHNOLOGY, 2006, 34 (02) : 191 - 199
  • [28] CULTIVATION OF MAMMALIAN-CELLS IN SERUM-FREE MEDIUM
    CHANDLER, JP
    AMERICAN BIOTECHNOLOGY LABORATORY, 1990, 8 (01): : 18 - &
  • [29] Adaptation of mammalian cells to growth in serum-free media
    Sinacore, MS
    Drapeau, D
    Adamson, SR
    MOLECULAR BIOTECHNOLOGY, 2000, 15 (03) : 249 - 257
  • [30] Adaptation of mammalian cells to growth in serum-free media
    Martin S. Sinacore
    Denis Drapeau
    S. R. Adamson
    Molecular Biotechnology, 2000, 15 : 249 - 257