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Factors to consider in performing survival studies with insect cells
Authors:Thomas M Koval
Institution:(1) George Washington University School of Medicine and Health Sciences, 20037 Washington, D. C.;(2) National Council on Radiation Protection and Measurements, 7910 Woodmont Avenue Suite 1016, 20814 Bethesda, Maryland
Abstract:Summary Insect cell lines are not well-suited to colony formation in liquid medium following low-density cell plating. The present studies demonstrate that the time of addition of fetal bovine serum to the culture medium and the number of γ-irradiated feeder cells added to each plate are important factors in developing a useful colony formation assay. TN-368 lepidopteran and WR69-DM-1 dipteran cell lines were used for these experiments. Both cell types display increased plating efficiencies if serum is added to the medium one or more days prior to plating as compared to adding serum immediately before plating. Growth curves obtained by seeding cells at higher densities also indicate that cell growth is slightly better if serum is added one or more days before seeding. These findings are especially important for survival and toxicity studies because the results demonstrate that even seemingly minor factors involved in cell survival assays may benefit treated cells to a greater degree than untreated control cells, thus providing an erroneous assessment of cell survival. This work was supported by USPHS grant R01-CA34158, awarded by the National Cancer Institute, DHHS, Bethesda, MD.
Keywords:insect cell culture  cell survival  colony formation  serum  feeder cells  toxicity studies
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