Skip to main content

Advertisement

Log in

pH Condition in temperature shift cultivation enhances cell longevity and specific hMab productivity in CHO culture

  • Special Issue JAACT
  • Published:
Cytotechnology Aims and scope Submit manuscript

Abstract

Controlling cell proliferation during cell culturing is an effective way to improve the production yield in mammalian cell culture. We examined the effect of temperature shifts (TS) under pH control conditions in Chinese hamster ovary cells. When we shifted the culture temperature from 37 °C to 31 °C before a stationary phase at pH 6.8 (TS/pH 6.8), cell viability remained high, and the final human monoclonal antibody (hMab) concentration increased to 2.3 times that in the culture remaining at 37 °C. However, there were no significant effects on the cell viability or production yield with the same TS at pH 7.0 (TS/pH 7.0). The average specific hMab productivity and mRNA level of TS/pH 7.0 were the same as that of TS/pH 6.8. The control of cell growth by the TS or the addition of rapamycin was effective in the maintenance of cell viability, but there was no significant increase of the average specific hMab productivity in the culture where cell proliferation was controlled with rapamycin. The hMab mRNA concentration decreased to 55%–65% at a 37 °C culture with the addition of actinomycin D. In contrast, actinomycin D did not affect the mRNA level in the TS culture. This result suggested that the increase in the mRNA level in the TS condition was caused by an increase in mRNA stability. In this study, we show that TS can produce two unrelated effects: a prolongation of cell longevity and an improvement in mRNA stability.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

Abbreviations

CHO cell:

Chinese hamster ovary cell

HC:

Heavy chain

hMab:

Human monoclonal antibody

IVCD:

Integral of viable cell density

LC:

Light chain

TS:

Temperature shift

TS/pH 6.8:

Temperature shift cultivation, pH 6.8

TS/pH 7.0:

Temperature shift cultivation, pH 7.0

VCD:

Viable cell density

37 °C/pH 6.8:

Culture at 37 °C, pH 6.8

37 °C/pH 7.0:

Culture at 37 °C, pH 7.0

References

  • Balcarcel RR, Stephanopoulos G (2001) Rapamycin reduces hybridoma cell death and enhances monoclonal antibody production. Biotechnol Bioeng 76:1–10

    Article  CAS  Google Scholar 

  • Bloemkolk J, Gray MR, Merchant F, Mosmann TR (1992) Effect of temperature on hybridoma cell cycle and Mab production. Biotechnol Bioeng 40:427–431

    Article  CAS  Google Scholar 

  • Ducommun P, Ruffieux P, Kadouri A, Stockar U, Marison I (2002) Monitoring of temperature effects on animal cell metabolism in a packed bed process. Biotechnol Bioeng 77:838–842

    Article  CAS  Google Scholar 

  • Fox SR, Patel UA, Yap MGS, Wang DC (2004) Maximizing interferon-γ production by chinese hamster ovary cells through temperature shift optimization: Experimental and modeling. Biotechnol Bioeng 85:177–184

    Article  CAS  Google Scholar 

  • Giard DJ, Fleischaker RJ, Fabricant M (1982) Effect of temperature on the production of human fibroblast interferon. Proc Soc Exp Biol Med 170:155–159

    CAS  Google Scholar 

  • Hendrick H, Winnepenninckx P, Abdelkafi C, Vandeputte O, Cherlet M, Marique T, Renemann G, Loa A, Kretzmer G, Werenne J (2001) Increased productivity of recombinant tissular plasminogen activator (t-PA) by butyrate and shift of temperature: a cell cycle phases analysis. Cytotechnology 36:71–83

    Article  CAS  Google Scholar 

  • Hung DT, Jamison TF, Schreiber SL (1996) Understanding and controlling the cell cycle with natural products. Chem Biol 3:623–639

    Article  CAS  Google Scholar 

  • Kaufmann H, Mazur X, Fussenegger M, Bailey JE (1999) Influence of low temperature on productivity, proteome and protein phosphorylation of CHO cells. Biotechnol Bioeng 63:573–582

    Article  CAS  Google Scholar 

  • Kaufmann H, Mazur X, Marone R, Bailey JE (2001) Comparative analysis of two controlled proliferation strategies regarding product quality, influence on tetracycline-regulated gene expression, and productivity. Biotechnol Bioeng 72:592–602

    Article  CAS  Google Scholar 

  • Nishiyama H, Itoh K, Kaneko Y, Kishishita M, Yoshida O, Fujita J (1997) A glycine-rich RNA-binding protein mediating cold-inducible suppression of mammalian cell growth. J Cell Biol 137:899–908

    Article  CAS  Google Scholar 

  • Paul A, Brune K (2002) Stabilization of gene expression profiles in blood after phlebotomy. Clin Chem 48:2251–2253

    Google Scholar 

  • Ryu JS, Kim TK, Chung JY, Lee GM (2000) Osmoprotective effect of glycine betaine on foreign protein production in hyperosmotic recombinant chinese hamster ovary cell cultures differs among cell lines. Biotechnol Bioeng 70:167–175

    Article  CAS  Google Scholar 

  • Reff ME (1997) Impaired dominant selectable marker sequence and intronic insertion strategies for enhancement of expression of gene product and expression vector systems comprising same. US Patent 5.648.267

  • Reuveny S, Kim YJ, Kemp CW, Shiloach J (1993) Effect of temperature and oxygen on cell growth and recombinant protein production in insect cell cultures. Applied Microbiol Biotechnol 38:619–623

    Article  CAS  Google Scholar 

  • Sauer PW, Burky JE, Wesson MC, Sternard HD, Qu L (2000) A high-yielding, generic-fed batch cell culture process for production of recombinant antibodies. Biotechnol Bioeng 67:585–597

    Article  CAS  Google Scholar 

  • Schatz SM, Kerschbaumer RJ, Gerstenbauer G, Kral M, Dorner F, Scheiflinger F (2003) Higher expression of Fab antibody fragments in a CHO cell line at reduced temperature. Biotechnol Bioeng 84:433–438

    Article  CAS  Google Scholar 

  • Sureshkumar GK, Mutharasan R (1991) The influence of temperature on a mouse–mouse hybridoma growth and monoclonal antibody production. Biotechnol Bioeng 37:292–295

    Article  CAS  Google Scholar 

  • Varley J, Birch J (1999) Reactor design for large scale suspension animal cell culture. Cytotechnology 29:177–205

    Article  CAS  Google Scholar 

  • Watanabe S, Shuttleworth J, Al-Rubeai M (2002) Regulation of cell cycle and productivity in NS0 cells by the over-expression of p21CIP1. Biotechnol Bioeng 77:1–7

    Article  CAS  Google Scholar 

  • Weidemann R, Ludwig A, Kretzmer G (1994) Low temperature cultivation – A step towards process optimisation. Cytotechnology 15:111–116

    Article  CAS  Google Scholar 

  • Yoon SK, Song JY, Lee GM (2003) Effect of low temperature on specific productivity, transcription level, and heterogeneity of erythropoietin in chinese hamster ovary cells. Biotechnol Bioeng 82:289–298

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Satoshi Oguchi.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Oguchi, S., Saito, H., Tsukahara, M. et al. pH Condition in temperature shift cultivation enhances cell longevity and specific hMab productivity in CHO culture. Cytotechnology 52, 199–207 (2006). https://doi.org/10.1007/s10616-007-9059-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10616-007-9059-2

Keywords

Navigation