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
收藏
页码:71 / 83
页数:12
相关论文
共 50 条
  • [21] Production of Lentiviral Vectors Encoding Recombinant Factor VIII Expression in Serum-Free Suspension Cultures
    Caron, Angelo Luis
    Picanco-Castro, Virginia
    Ansorge, Sven
    Covas, Dimas Tadeu
    Kamen, Amine
    Swiech, Kamilla
    BRAZILIAN ARCHIVES OF BIOLOGY AND TECHNOLOGY, 2015, 58 (06) : 923 - 928
  • [22] Characterization of human dental pulp cells grown in chemically defined serum-free medium
    Fujii, Sakiko
    Fujimoto, Katsumi
    Goto, Noriko
    Abiko, Yoshimitsu
    Imaoka, Asayo
    Shao, Jinchang
    Kitayama, Kazuko
    Kanawa, Masami
    Sosiawan, Agung
    Suardita, Ketut
    Nishimura, Fusanori
    Kato, Yukio
    BIOMEDICAL REPORTS, 2018, 8 (04) : 350 - 358
  • [23] Harvesting and concentration of human influenza A virus produced in serum-free mammalian cell culture for the production of vaccines
    Kalbfuss, Bernd
    Genzel, Yvonne
    Wolff, Michael
    Zimmermann, Anke
    Morenweiser, Robert
    Reichl, Udo
    BIOTECHNOLOGY AND BIOENGINEERING, 2007, 97 (01) : 73 - 85
  • [24] SERUM-FREE CULTURE OF CARCINOMA CELL-LINES
    COLLODI, P
    RAWSON, C
    BARNES, D
    CYTOTECHNOLOGY, 1991, 5 (01) : 31 - 46
  • [25] High-titer, serum-free production of adeno-associated virus vectors by polyethyleneimine-mediated plasmid transfection in mammalian suspension cells
    Hildinger, Markus
    Baldi, Lucia
    Stettler, Matthieu
    Wurm, Florian M.
    BIOTECHNOLOGY LETTERS, 2007, 29 (11) : 1713 - 1721
  • [26] Derivation and characterization of human embryonic germ cells: serum-free culture and differentiation potential
    Hua, Jinlian
    Yu, Haisheng
    Liu, Sheng
    Dou, Zhongying
    Sun, Yadong
    Jing, Xiaoqi
    Yang, Chunrong
    Lei, Anmin
    Wang, Huayan
    Gao, Zhimin
    REPRODUCTIVE BIOMEDICINE ONLINE, 2009, 19 (02) : 238 - 249
  • [27] Feeder layer- and serum-free culture of rhesus monkey embryonic stem cells
    Zhang, Xiuzhen
    Wang, Shufen
    Yang, Shihua
    Li, Tianqing
    Ji, Shaohui
    Chen, Hongwei
    Li, Bin
    Jin, Lifang
    Xie, Yunhua
    Hu, Zhixing
    Chi, Jianxiang
    REPRODUCTIVE BIOMEDICINE ONLINE, 2006, 13 (03) : 412 - 420
  • [28] High-titer, serum-free production of adeno-associated virus vectors by polyethyleneimine-mediated plasmid transfection in mammalian suspension cells
    Markus Hildinger
    Lucia Baldi
    Matthieu Stettler
    Florian M. Wurm
    Biotechnology Letters, 2007, 29 : 1713 - 1721
  • [29] EXPANSION OF NATURAL KILLER CELLS USING A SERUM-FREE AND FEEDER CELL-FREE CULTURE PROTOCOL
    Frary, E.
    Johnson, C.
    Nazaire, C.
    Van-Etten, J.
    Faulkner, B.
    Hermanson, D.
    Flynn, K.
    Jesuraj, N. J.
    Lomakin, J.
    CYTOTHERAPY, 2021, 23 (05) : S107 - S107
  • [30] Culture of porcine hepatocytes or bile duct epithelial cells by inductive serum-free media
    Thomas J. Caperna
    Le Ann Blomberg
    Wesley M. Garrett
    Neil C. Talbot
    In Vitro Cellular & Developmental Biology - Animal, 2011, 47 : 218 - 233