Abstract
A replication deficient adenovirus containing the measles virus N gene (nucleoprotein) was propagated on a specially constructed mammalian helper cell line (293), and used to infect a target cell population (MRC5) where expression of the cloned gene only is obtained from the strong CMV IE promoter. Electron microscopy showed that the N protein accumulates in both the cytoplasm and nucleus of infected cells. The growth of 293 cells was compared in a variety of cell culture systems including static flasks, cell aggregates and a variety of microcarriers. The best results were achieved using the Fibra-cel carrier. Virus yields were comparable with the Fibra-cel carriers, cell aggregates and static flasks.
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© 1995 Springer Science+Business Media Dordrecht
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Fooks, A.R. et al. (1995). Preliminary Studies With Scaleable Systems for the Production of Replication-Deficient Recombinant Adenoviruses in Mammalian Cell Lines. In: Beuvery, E.C., Griffiths, J.B., Zeijlemaker, W.P. (eds) Animal Cell Technology: Developments Towards the 21st Century. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-0437-1_4
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DOI: https://doi.org/10.1007/978-94-011-0437-1_4
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