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Establishment of Novel Cell Line for Bioartificial Liver

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Animal Cell Technology: Basic & Applied Aspects

Part of the book series: Animal Cell Technology: Basic & Applied Aspects ((ANICELLTECH,volume 12))

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Abstract

Though livers from cadavers being transplanted, more patients are waiting the grafting. Because of this shortage of the donation, artificial liver is expected. But at present, artificial livers do not satisfy the patients yet. In this study, we attempted to establish novel hepatoma cell line for better artificial liver. We have ever introduced anti-apoptosis gene into hybridoma cells and this transfection delayed cell death. Because of this prolonging culture, the transfectants produce 2 times more antibodies than wild type. For the longer-term or permanent artificial liver, we introduced bd-2, anti-apoptosis gene, to HepG2 hepatoma cell.

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References

  1. Starzl TE et al., `Baboon-to-human liver transplantation.“ Surgery 71, 537 (1993)

    Google Scholar 

  2. Strom CS et al., “Hepatocyte transplantation as a bridge to orthotopic liver transplantation in terminal liver failure.” Transplantation, 63, 559–569 (1997)

    Article  PubMed  CAS  Google Scholar 

  3. Matsumura KN et al., “Hybrid bioartificial liver in hepatic failure: preliminary clinical report.” Surgery, 101, 99 (1987)

    PubMed  CAS  Google Scholar 

  4. Jauregui HO, et al. “Mammalian hepatocyte as a foundation for treatment in human liver failure.” J. Cell. Biochem. 43, 359 (1991)

    Article  Google Scholar 

  5. Nyberg SL et al., ‘Primary hepatocytes outperform hep G2 cells as the source of biotransformation functions in a bioartificial lover.“ Ann. Surg. 220, 59–67 (1994)

    PubMed  CAS  Google Scholar 

  6. Kelly JH et al., The hepatex extracorporeal liver assist device in the treatment of fullminant hepatic failure.“ ASAIO J. 40, 83–85 (1994)

    CAS  Google Scholar 

  7. Rozga J. et al., “A bioartificial liver to treat severe acute liver failure.” Ann. Surg., 219, 538546 (1994)

    Google Scholar 

  8. Pattersson M et.al. “Expression of the bcl-2 gene in human multiple myeloma cell lines and normal plasma cells”. Blood 79, 495–502 (1992)

    Google Scholar 

  9. Itoh Y et.al. ‘Over-expression of bel-2, apoptosis suppressing gene, prolonged viable culture period of hybridoma and enhanced antibody production“ Biotechnol. Bioeng. 48, 118–122 (1995)

    Article  Google Scholar 

  10. Terada S et.al. “Characterization and fed-batch culture of hybridoma overexpressing apoptosis suppressing gene bcl-2.’ Cytotechnology 24, 135–141 (1997)

    Article  Google Scholar 

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© 2002 Springer Science+Business Media Dordrecht

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Terada, S. et al. (2002). Establishment of Novel Cell Line for Bioartificial Liver. In: Shirahata, S., Teruya, K., Katakura, Y. (eds) Animal Cell Technology: Basic & Applied Aspects. Animal Cell Technology: Basic & Applied Aspects, vol 12. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-0728-2_36

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  • DOI: https://doi.org/10.1007/978-94-017-0728-2_36

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-90-481-5934-5

  • Online ISBN: 978-94-017-0728-2

  • eBook Packages: Springer Book Archive

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