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Transferrin recycling perfusion culture of hybridoma cells

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Abstract

A perfusion culture of hybridoma cells in serum-free medium recycling transferrin was carried out, which greatly reduced the level of transferrin that was needed. The culture was maintained even without supplying transferrin for nine days. IgG concentration reached 1.1 mg ml−1 in a month of recycling and its ratio to the total protein was 45.8%. The affinity of the antibody did not decrease and no degradation was observed after long recycling period. The cell density under recycling condition was 2≈3 times higher than that without recycling. It was indicated that there was autocrine growth promoting activity in the culture supernatant.

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References

  • Altshuler GL, Dziewulski DM, Sowek JA and Belfort G (1985) Continuous hybridoma growth and monoclonal antibody production in hollow fiber reactors-separators. Biotechnol. Bioeng. 28: 646–658.

    Article  Google Scholar 

  • Basset P, Quesneau Y and Zwiller J (1986) Iron-induced L1210 cell growth: evidence of a transferrin-independent iron transport Cancer Res. 46: 1644–1647.

    CAS  Google Scholar 

  • Duff RG (1985) Microencapsulation technology: a novel method for monoclonal antibody production. Trends Biotechnol. 3: 167–170.

    Article  Google Scholar 

  • Gilligan KJ, Littlefield S and Jarvis A Jr (1988) Production of rat monoclonal antibody from rat × mouse hybridoma cell lines using microencapsulation technology. In Vitro 24: 35–41.

    CAS  Google Scholar 

  • Glacken MW (1988) Catabolic control of mammalian cell culture. Bio/Technology 6:1041–1050.

    Article  CAS  Google Scholar 

  • Hamamoto K, Ishimaru K and Tokashiki M (1989) Perfusion culture of hybridoma cells using a centrifuge to separate cells from culture mixture, J. Ferment. Bioeng. 67: 190–194.

    Article  Google Scholar 

  • King GA, Daugulis AJ, Faulkner P and Goosen MFA (1987) Alginate-polylysine microcapsule of controlled membrane molecular weight cutoff for mammalian cell culture engineering. Biotechnol. Progr. 3: 231–240.

    Article  CAS  Google Scholar 

  • Klausner RD, Renswoude JV, Ashwell G, Kempf C, Schechter AN, Dean A and Bridges KR (1983) Receptor-mediated endocytosis of transferrin in K562 cells. J. Biol. Chem. 258: 4715–4724.

    CAS  Google Scholar 

  • Lauffenburger D and Cozens C (1989) Regulation of mammalian cell growth by autocrine growth factors: analysis of consequences for inoculum cell density effects. Biotechnol. Bioeng. 33: 1365–1378.

    Article  CAS  Google Scholar 

  • Lehmann J, Kempken R, Lutkemeyer D and Buntemeyer H (1989) Economic aspects of medium recycling. Proceedings of the Second Annual Meeting of the Japanese Association for Animal Cell Technology; pp. 55–59.

  • Murakami H, Masui H, Sato GH, Sueoka N, Chow TP and Kano-Sueoka T (1982) Growth of hybridoma cells in serumfree medium. Proc. Natl. Acad. Sci., USA 79: 1158–1162.

    Article  CAS  Google Scholar 

  • Murakami H, Shimomura T, Nakamura T, Ohashi H, Shinohara K and Omura H (1984) Development of a basal medium for serum-free cultivation of hybridoma cells in high density. Nippon Nougeikagaku Kaishi 58: 575–583.

    CAS  Google Scholar 

  • Rasmussen L and Toftlund H (1986) Phosphate compounds as iron chelators in animal cell cultures. In Vitro 22: 177–179.

    CAS  Google Scholar 

  • Takazawa Y, Tokashiki M, Hamamoto K and Murakami H (1988) High cell density perfusion culture of hybridoma cells recycling high molecular weight components. Cytotechnology 1: 171–178.

    Article  Google Scholar 

  • Tokashiki M, Takazawa Y and Hamamoto K (1987) High density culture of hybridoma cells using a perfusion culture vessel with filter. Hakko Kogaku Kaishi 65: 535–536.

    Google Scholar 

  • Tokashiki M, Hamamoto K, Takazawa Y and Ichikawa Y (1988) High-density culture of mouse-human hybridoma cells using a new perfusion culture vessel. Kagaku Kogaku Ronbunshu 14: 337–341.

    CAS  Google Scholar 

  • Yabe N (1987) Role of iron chelators in growth-promoting effect on mouse hybridoma cells in a chemically defined medium. Soshikibaiyou 13: 13–16.

    Google Scholar 

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Takazawa, Y., Tokashiki, M. Transferrin recycling perfusion culture of hybridoma cells. Cytotechnology 8, 189–194 (1992). https://doi.org/10.1007/BF02522035

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  • DOI: https://doi.org/10.1007/BF02522035

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