Summary
Studies conducted with virus-infected monolayer cell cultures have demonstrated the feasibility of producing several tumor-associated viruses in microcarrier (mc) cultures (Sephadex G50 beads treated with DEAE-chloride). The efficiency of cell adherence to mc varied with the cell type, the pH of the growth medium, and the stirring force applied to keep the mc in suspension. Most cells attached firmly to the mc and could not be removed easily with routine trypsinization procedures. Techniques using Enzar-T and Pronase were effective in detaching cells from mc in 10 to 15 min while retaining 95% cell viability. After detachment, Ficoll gradients were used for rapid and complete separation of viable cell suspensions from the mc. Retrovirus production in large volumes of mc cultures was investigated with periodic harvesting of growth fluids. Physical, biochemical, and biological properties of the Mason-Pfizer monkey virus and the RD114 virus recovered from the mc cultures were identical to those produced in conventional cultures. The utilization of mc has several applications in research and short-term cultures, but the as-yet-unsolved technical problems met were found to be serious limitations when attempting mass cell culturing on a long-term basis.
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For reprint requests address: Dr. Keith Jensen, Pfizer, Inc., Groton, CT 06340.
This work was supported in part under contract N01-CP-33234 within the Virus Cancer Program of the National Cancer Institute.
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Manousos, M., Ahmed, M., Torchio, C. et al. Feasibility studies of oncornavirus production in microcarrier cultures. In Vitro 16, 507–515 (1980). https://doi.org/10.1007/BF02626464
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DOI: https://doi.org/10.1007/BF02626464