Enhancing Effect of Low Culture Temperature on Specific Antibody Productivity of Recombinant Chinese Hamster Ovary Cells: Clonal Variation

To understand the different responses of recombinant Chinese hamster ovary (rCHO) cells to low culture temperature regarding specific productivity ( q), 12 parental clones and their corresponding amplified clones producing a humanized antibody were cultivated at 32 and 37 °C. The specific growth rate of all clones, including both parental and amplified clones, decreased by 30–63% at 32 °C, compared to rates at 37°C. In contrast, their specific antibody productivity ( qAb) was significantly enhanced at 32 °C. Furthermore, the degree of qAb enhancement at 32 °C varied a lot from 4‐ to 25‐fold among the parental clones. At 32 °C, most of the amplified clones, regardless of methotrexate (MTX) levels, also showed enhanced qAb but to a lesser extent than their parental clones. However, clone 14 amplified at 0.32 μM MTX (clone 14–0.32) and clone 20 amplified at 1 μM MTX (clone 20–1.00), unlike their parental clones, did not show enhanced qAb at 32 °C. Thus, it was found that the enhancing effect of low culture temperature on q of rCHO cells depends on clones. Taken together, the results obtained here emphasize the importance of clonal selection for the successful application of low culture temperature to the enhanced foreign protein production in rCHO cells.

[1]  Michimasa Kishimoto,et al.  Evaluation of stable and highly productive gene amplified CHO cell line based on the location of amplified genes , 2000, Cytotechnology.

[2]  G. Kretzmer,et al.  Increased productivity of recombinant tissular plasminogen activator (t-PA) by butyrate and shift of temperature: a cell cycle phases analysis , 2001, Cytotechnology.

[3]  S. Bae,et al.  Decreased chimeric antibody productivity of KR12H‐1 transfectoma during long‐term culture results from decreased antibody gene copy number , 2000, Biotechnology and bioengineering.

[4]  K. Furukawa,et al.  Effect of culture temperature on a recombinant CHO cell line producing a C-terminal α-amidating enzyme , 1998, Cytotechnology.

[5]  J E Bailey,et al.  Influence of low temperature on productivity, proteome and protein phosphorylation of CHO cells. , 1999, Biotechnology and bioengineering.

[6]  T Etcheverry,et al.  Performance of small-scale CHO perfusion cultures using an acoustic cell filtration device for cell retention: characterization of separation efficiency and impact of perfusion on product quality. , 2000, Biotechnology and bioengineering.

[7]  C. Ryu,et al.  Characterization of chimeric antibody producing CHO cells in the course of dihydrofolate reductase-mediated gene amplification and their stability in the absence of selective pressure. , 1998, Biotechnology and bioengineering.

[8]  J. Davies,et al.  Chromosome localization and gene‐copy‐number quantification of three random integrations in Chinese‐hamster ovary cells and their amplified cell lines using fluorescence in situ hybridization , 2001, Biotechnology and applied biochemistry.

[9]  Sung Hyun Kim,et al.  Effect of Low Culture Temperature on Specific Productivity and Transcription Level of Anti‐4–1BB Antibody in Recombinant Chinese Hamster Ovary Cells , 2008, Biotechnology progress.

[10]  W. Flintoff,et al.  Moderate-level gene amplification in methotrexate-resistant Chinese hamster ovary cells is accompanied by chromosomal translocations at or near the site of the amplified DHFR gene , 1984, Molecular and cellular biology.

[11]  G. Lee,et al.  Osmoprotective Effect of Glycine Betaine on Thrombopoietin Production in Hyperosmotic Chinese Hamster Ovary Cell Culture: Clonal Variations , 2000, Biotechnology progress.

[12]  B. Howard,et al.  Expression of recombinant plasmids in mammalian cells is enhanced by sodium butyrate. , 1983, Nucleic acids research.

[13]  Kazuaki Furukawa,et al.  Enhancement of productivity of recombinant α-amidating enzyme by low temperature culture , 1999, Cytotechnology.

[14]  Katsuhiko Itoh,et al.  A Glycine-rich RNA-binding Protein Mediating Cold-inducible Suppression of Mammalian Cell Growth , 1997, The Journal of cell biology.

[15]  A. Dorner,et al.  Increased synthesis of secreted proteins induces expression of glucose-regulated proteins in butyrate-treated Chinese hamster ovary cells. , 1989, The Journal of biological chemistry.

[16]  Gyun Min Lee,et al.  Effect of low culture temperature on specific productivity, transcription level, and heterogeneity of erythropoietin in Chinese hamster ovary cells. , 2003, Biotechnology and bioengineering.

[17]  J E Bailey,et al.  Comparative analysis of two controlled proliferation strategies regarding product quality, influence on tetracycline-regulated gene expression, and productivity. , 2001, Biotechnology and bioengineering.

[18]  Y. Ahn,et al.  Influence of reducing agents on the secretion rate of recombinant erythropoietin from CHO cells , 1998, Biotechnology Letters.

[19]  D K Robinson,et al.  Industrial choices for protein production by large-scale cell culture. , 2001, Current opinion in biotechnology.