Literature DB >> 15981277

Optimization of tetracycline-responsive recombinant protein production and effect on cell growth and ER stress in mammalian cells.

Jullian Jones1, Tarangsri Nivitchanyong, Christina Giblin, Valentina Ciccarone, David Judd, Stephen Gorfien, Sharon S Krag, Michael J Betenbaugh.   

Abstract

The inducible T-REx system and other inducible expression systems have been developed in order to control the expression levels of recombinant protein in mammalian cells. In order to study the effects of heterologous protein expression on mammalian host behavior, the gene for recombinant Human transferrin (hTf) was integrated into HEK-293 cells and expressed under the control of the T-REx inducible technology (293-TetR-Hyg-hTf) or using a constitutive promoter (293-CMV-hTf). A number of inducible clones with variable expression levels were identified for the T-REx system with levels of hTf for the high expressing clones nearly double those obtained using the constitutive cytomegalovirus (CMV) promoter. The level of transferrin produced was found to increase proportionately with tetracycline concentration between 0 and 1 mug/mL with no significant increases in transferrin production above 1 mug/mL. As a result, the optimal induction time and tetracycline concentrations were determined to be the day of plating and 1 mug/mL, respectively. Interestingly, the cells induced to express transferrin, 293-TetR-Hyg-hTf, exhibited lower viable cell densities and percent viabilities than the uninduced cultures for multiple clonal isolates. In addition, the induction of transferrin expression was found to cause an increase in the expression of the ER-stress gene, BiP, that was not observed in the uninduced cells. However, both uninduced and induced cell lines containing the hTf gene exhibited longer survival in culture than the control cells, possibly as a result of the positive effects of hTf on cell survival. Taken together, these results suggest that the high level expression of complex proteins in mammalian cells can limit the viable cell densities of cells in culture as a result of cellular stresses caused by generating proteins that may be difficult to fold or are otherwise toxic to cells. The application of inducible systems such as the T-REx technology will allow us to optimize protein production while limiting the negative effects that result from these cellular stresses. (c) 2005 Wiley Periodicals, Inc.

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Year:  2005        PMID: 15981277     DOI: 10.1002/bit.20566

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  13 in total

1.  Blocking of melatonin synthesis and MT(1) receptor impairs the activation of Jurkat T cells.

Authors:  Patricia J Lardone; Amalia Rubio; Isabel Cerrillo; Araceli Gómez-Corvera; Antonio Carrillo-Vico; Marina Sanchez-Hidalgo; Juan M Guerrero; Patricia Fernandez-Riejos; Victor Sanchez-Margalet; Patrocinio Molinero
Journal:  Cell Mol Life Sci       Date:  2010-05-04       Impact factor: 9.261

2.  Controllable Ion Channel Expression through Inducible Transient Transfection.

Authors:  Matan Geron; Adina Hazan; Avi Priel
Journal:  J Vis Exp       Date:  2017-02-17       Impact factor: 1.355

3.  Transgenic mouse and cell culture models demonstrate a lack of mechanistic connection between endoplasmic reticulum stress and tau dysfunction.

Authors:  M L Spatara; A S Robinson
Journal:  J Neurosci Res       Date:  2010-07       Impact factor: 4.164

4.  Efficient CRISPR/Cas9 nickase-mediated genome editing in an in vitro model of mucopolysaccharidosis IVA.

Authors:  Andrés Felipe Leal; Carlos Javier Alméciga-Díaz
Journal:  Gene Ther       Date:  2022-05-18       Impact factor: 5.250

5.  Inducible, tightly regulated and non-leaky neuronal gene expression in mice.

Authors:  Fabien Delerue; Michael White; Lars M Ittner
Journal:  Transgenic Res       Date:  2013-11-09       Impact factor: 2.788

6.  The cumate gene-switch: a system for regulated expression in mammalian cells.

Authors:  Alaka Mullick; Yan Xu; René Warren; Maria Koutroumanis; Claire Guilbault; Sophie Broussau; Félix Malenfant; Lucie Bourget; Linda Lamoureux; Rita Lo; Antoine W Caron; Amelie Pilotte; Bernard Massie
Journal:  BMC Biotechnol       Date:  2006-11-03       Impact factor: 2.563

7.  Engineering of chaperone systems and of the unfolded protein response.

Authors:  Saeed U Khan; Martin Schröder
Journal:  Cytotechnology       Date:  2008-08-15       Impact factor: 2.058

8.  Decoupling Growth and Protein Production in CHO Cells: A Targeted Approach.

Authors:  James S Donaldson; Matthew P Dale; Susan J Rosser
Journal:  Front Bioeng Biotechnol       Date:  2021-06-02

9.  Transferring a synthetic gene circuit from yeast to mammalian cells.

Authors:  Dmitry Nevozhay; Tomasz Zal; Gábor Balázsi
Journal:  Nat Commun       Date:  2013       Impact factor: 14.919

10.  Optimization of heterologous protein production in Chinese hamster ovary cells under overexpression of spliced form of human X-box binding protein.

Authors:  Galina Gulis; Kelly Cristina Rodrigues Simi; Renata Rodrigues de Toledo; Andrea Queiroz Maranhao; Marcelo Macedo Brigido
Journal:  BMC Biotechnol       Date:  2014-04-11       Impact factor: 2.563

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