Literature DB >> 19003357

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

E J Schlaeger1, K Christensen.   

Abstract

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 mug/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 mug/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 mug/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.

Entities:  

Year:  1999        PMID: 19003357      PMCID: PMC3449952          DOI: 10.1023/A:1008000327766

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  26 in total

1.  Coupling of cell-binding ligands to polyethylenimine for targeted gene delivery.

Authors:  R Kircheis; A Kichler; G Wallner; M Kursa; M Ogris; T Felzmann; M Buchberger; E Wagner
Journal:  Gene Ther       Date:  1997-05       Impact factor: 5.250

2.  Characteristics of a human cell line transformed by DNA from human adenovirus type 5.

Authors:  F L Graham; J Smiley; W C Russell; R Nairn
Journal:  J Gen Virol       Date:  1977-07       Impact factor: 3.891

3.  Soluble receptors for tumor necrosis factor as predictors of progression to AIDS in asymptomatic human immunodeficiency virus type 1 infection.

Authors:  M H Godfried; T van der Poll; G J Weverling; J W Mulder; J Jansen; S J van Deventer; H P Sauerwein
Journal:  J Infect Dis       Date:  1994-04       Impact factor: 5.226

4.  The protein hydrolysate, Primatone RL, is a cost-effective multiple growth promoter of mammalian cell culture in serum-containing and serum-free media and displays anti-apoptosis properties.

Authors:  E J Schlaeger
Journal:  J Immunol Methods       Date:  1996-08-14       Impact factor: 2.303

5.  Molecular cloning and expression of the human 55 kd tumor necrosis factor receptor.

Authors:  H Loetscher; Y C Pan; H W Lahm; R Gentz; M Brockhaus; H Tabuchi; W Lesslauer
Journal:  Cell       Date:  1990-04-20       Impact factor: 41.582

6.  Improved expression cloning using reporter genes and Epstein-Barr virus ori-containing vectors.

Authors:  E S Shen; G M Cooke; R A Horlick
Journal:  Gene       Date:  1995-04-24       Impact factor: 3.688

7.  Scale-up of the adenovirus expression system for the production of recombinant protein in human 293S cells.

Authors:  A Garnier; J Côté; I Nadeau; A Kamen; B Massie
Journal:  Cytotechnology       Date:  1994       Impact factor: 2.058

8.  Transfecting mammalian cells: optimization of critical parameters affecting calcium-phosphate precipitate formation.

Authors:  M Jordan; A Schallhorn; F M Wurm
Journal:  Nucleic Acids Res       Date:  1996-02-15       Impact factor: 16.971

9.  A versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo: polyethylenimine.

Authors:  O Boussif; F Lezoualc'h; M A Zanta; M D Mergny; D Scherman; B Demeneix; J P Behr
Journal:  Proc Natl Acad Sci U S A       Date:  1995-08-01       Impact factor: 11.205

10.  Optimization of culture conditions for high cell density proliferation of HL-60 human promyelocytic leukemia cells.

Authors:  B Schumpp; E J Schlaeger
Journal:  J Cell Sci       Date:  1990-12       Impact factor: 5.285

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  27 in total

1.  Non-GMP plasmid production for transient transfection in bioreactors.

Authors:  G Schmid; E J Schlaeger; B Wipf
Journal:  Cytotechnology       Date:  2001-05       Impact factor: 2.058

2.  Effect of addition of 'carrier' DNA during transient protein expression in suspension CHO culture.

Authors:  Ketaki Pradhan; Mugdha Gadgil
Journal:  Cytotechnology       Date:  2012-03-14       Impact factor: 2.058

3.  Serum-free suspension large-scale transient transfection of CHO cells in WAVE bioreactors.

Authors:  Raj Haldankar; Danqing Li; Zane Saremi; Claudia Baikalov; Rohini Deshpande
Journal:  Mol Biotechnol       Date:  2006-10       Impact factor: 2.695

4.  Development of a generic transient transfection process at 100 L scale.

Authors:  Ola Tuvesson; Christina Uhe; Aleksei Rozkov; Elke Lüllau
Journal:  Cytotechnology       Date:  2008-02-22       Impact factor: 2.058

5.  Evaluation of a Serum-free Medium for the Production of rAAV-2 using HeLa Derived Producer Cells.

Authors:  C Jenny; E Toublanc; O Danos; O-W Merten
Journal:  Cytotechnology       Date:  2005-09       Impact factor: 2.058

Review 6.  Large-scale transfection of mammalian cells for the fast production of recombinant protein.

Authors:  Phuong Lan Pham; Amine Kamen; Yves Durocher
Journal:  Mol Biotechnol       Date:  2006-10       Impact factor: 2.695

7.  The transient expression of CHIKV VLP in large stirred tank bioreactors.

Authors:  Peifeng Chen; Jacob Demirji; Vera B Ivleva; Joe Horwitz; Richard Schwartz; Frank Arnold
Journal:  Cytotechnology       Date:  2019-09-27       Impact factor: 2.058

8.  Large-scale transient transfection of mammalian cells: a newly emerging attractive option for recombinant protein production.

Authors:  Sabine Geisse; Mario Henke
Journal:  J Struct Funct Genomics       Date:  2005

9.  Optimizing the transient transfection process of HEK-293 suspension cells for protein production by nucleotide ratio monitoring.

Authors:  Maria de Los Milagros Bassani Molinas; Christiane Beer; Friedemann Hesse; Manfred Wirth; Roland Wagner
Journal:  Cytotechnology       Date:  2013-06-18       Impact factor: 2.058

10.  High Yield Expression of Recombinant Human Proteins with the Transient Transfection of HEK293 Cells in Suspension.

Authors:  Ganesh P Subedi; Roy W Johnson; Heather A Moniz; Kelley W Moremen; Adam Barb
Journal:  J Vis Exp       Date:  2015-12-28       Impact factor: 1.355

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