Abstract
There is a genuine need in the biotechnology industry for the capability of growing, cheaply and efficiently, normal, untransformed, anchorage-dependent animal cells on a large scale. This need exists for the unique products that these cells may be capable of synthesizing, and in the case of esoteric cell types, such as chondrocytes, hepatocytes, etc., for the very cells themselves, as well as for the advantages inherent in the use of normal cells in biotechnology manufacturing. Unlike transformed cells, normal cells do not secrete large amounts of proteases nor produce truncated carbohydrate side chains; they do not harbor oncogenic viruses or activated oncogenes, which pose problems of regulatory and safety issues, and, at least theoretically, they should be able to continue to produce large amounts of protein while in the quiescent, noncycling state—the ideal condition for most efficient synthetic protein production. Unfortunately, unlike transformed cells, most normal animal cells are unable to grow in suspension, but require attachment to a solid substratum or extracellular matrix (anchorage-dependence). This makes their large-scale cultivation extremely costly and technically difficult.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Aebischer P, Tresco PA, Winn SR, Greene LA, Jaeger CB. 1991. Long-term cross-species brain transplantation of a polymer-encapsulated dopamine-secreting cell line. Exptl Neurol 111:269–275.
Bellamkonda R, Ranieri JP, Aebischer P. 1995. Laminin oligopeptide derivatized agarose gels allow threedimensional neurite extension in vitro. J Neurosci Res 41:501–509.
Croughan MS, Hamel J-F, Wang DIC. 1987. Hydrodynamic effects on animal cells grown in microcarrier cultures. Biotechnol Bioeng 29:130–141.
Croughan MS, Wang, DIC. 1989. Growth and death in overagitated microcarrier cell cultures. Biotechnol Bioeng 33:731–744.
Galletti PM, Aebischer P, Lysaght MJ. 1995. The dawn of biotechnology in artificial organs. ASAIO J. 41(1):49–57.
Gillies SD, Dorai H, Wesolowski J, Majeau G, Young D, Boyd J, Gardner J, James K. 1989. Expression of human anti-tetanus toxoid antibody in transfected murine myeloma cells. Biotechnol 7:799–804.
Jarvis Jr. AP, Grdina TA. 1983. Production of biologicals from microencapsulated living cells. Biotechniques 1:24–30.
Lim F, Moss RD. 1981. Microencapsulation of living cells and tissues. J Pharm Sei 70:351–354.
Matthew HWT, Basu S, Peterson WD, Salley SO, Klein MD. 1993a. Performance of plasma-perfused, microencapsulated hepatocytes: prospects for extracorporeal liver support. J Pediatr Surg 28(11):1423–1428.
Matthew HW, Salley SO, Peterson WD, Klein MD. 1993b. Complex coacervate microcapsules for mammalian cell culture and artificial organ development. Biotechnol Prog 9:510–519.
Posillico EG. 1986. Microencapsulation technology for large-scale antibody production. Bio/Technol 4:114–117.
Reuveny S. 1985. Microcarriers in cell culture: structure and applications. Adv Cell Cult 4:213–247.
Rupp RG. 1985. Use of cellular microencapsulation in large scale production of monoclonal antibodies. In: Feder J, Tolbert W, editors. Large scale mammalian cell culture. New York: Academic Press, p 19–38.
Rupp RG, Geyer SD. 1984. Preparation of medium for largescale hybridoma culture. J Tiss Cult Meth 8:141–146.
Sun Y-L, Ma X, Zhou D, Vacek I, Sun AM. 1993. Porcine pancreatic islets: isolation, microencapsulation, and xenotransplantation. Artif Organs 17(8):727–733.
Yoshioka T, Hirano R, Shioya T, Kako M. 1990. Encapsulation of mammalian cell with chitosan-CMC capsule. Biotechnol Bioeng 35:66–72.
Young DV, Dobbels S, King L, Deer F, Gillies SD. 1989. Inverted microcarriers: using microencapsulation to grow anchorage-dependent cells in suspension. BioPharm 2:34–46.
Young DV. 1992. Inverted microcarriers: Using microencapsulation to grow anchorage-dependent cells. In: Goosen MFA, editor. Fundamentals of animal cell encapsulation and immobilization. Boca Raton, Florida: CRC Press, p 243–265.
Zielinski BA, Aebischer P. 1994. Chitosan as a matrix for mammalian cell encapsulation. Biomaterials 15(13):1049–1056.
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1999 Springer Science+Business Media New York
About this chapter
Cite this chapter
Young, D.V. (1999). Culture of Anchorage-Dependent Cells. In: Kühtreiber, W.M., Lanza, R.P., Chick, W.L. (eds) Cell Encapsulation Technology and Therapeutics. Birkhäuser, Boston, MA. https://doi.org/10.1007/978-1-4612-1586-8_31
Download citation
DOI: https://doi.org/10.1007/978-1-4612-1586-8_31
Publisher Name: Birkhäuser, Boston, MA
Print ISBN: 978-1-4612-7205-2
Online ISBN: 978-1-4612-1586-8
eBook Packages: Springer Book Archive