Alteration of Growth Rate and Nutritional Requirement of Hamster Brain Cells Transformed by Adenovirus Type 12 during Their Long-term Cultivation
HT-2 cells, one of the hamster brain cell lines transformed by adenovirus type 12 in vitro, were serially cultivated. During their long-term cultivation, the altera-tion of their growth rate and nutritional requirement were examined. The growth rate of the cells gradually increased with advancing tr...
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Published in | The Tohoku Journal of Experimental Medicine Vol. 92; no. 3; pp. 257 - 264 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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Japan
Tohoku University Medical Press
01.01.1967
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Abstract | HT-2 cells, one of the hamster brain cell lines transformed by adenovirus type 12 in vitro, were serially cultivated. During their long-term cultivation, the altera-tion of their growth rate and nutritional requirement were examined. The growth rate of the cells gradually increased with advancing transfer generations. The bovine serum requirement of those cells was extremely high at their early passages, but after the 50th passage, 3% of serum could support sufficient cell growth at an inoculation density of 104 cells per ml. The comparison of growth rates of HT-2 cells of two different passages at various inoculation densities revealed increasing growth potentials during serial cultivation. Their limited growth rate in a closed gaseous system which had been reported previously remained stable all over the passage and could not be improved by various nutritional conditions. Further, growth characteristics of the cells in an open gaseous system without using a CO2 incubator suggested that they might need certain gas-circulating open condition to grow well. |
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AbstractList | HT-2 cells, one of the hamster brain cell lines transformed by adenovirus type 12 in vitro, were serially cultivated. During their long-term cultivation, the altera-tion of their growth rate and nutritional requirement were examined. The growth rate of the cells gradually increased with advancing transfer generations. The bovine serum requirement of those cells was extremely high at their early passages, but after the 50th passage, 3% of serum could support sufficient cell growth at an inoculation density of 104 cells per ml. The comparison of growth rates of HT-2 cells of two different passages at various inoculation densities revealed increasing growth potentials during serial cultivation. Their limited growth rate in a closed gaseous system which had been reported previously remained stable all over the passage and could not be improved by various nutritional conditions. Further, growth characteristics of the cells in an open gaseous system without using a CO2 incubator suggested that they might need certain gas-circulating open condition to grow well. |
Author | Yamane, Isao Koyama, Hideki Kusano, Toshihisa |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/6064506$$D View this record in MEDLINE/PubMed |
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References | 12) Todaro, G. J. & Green, H. Quantitative studies of the growth of mouse embryo cells in culture and their development into established lines. J. Cell Biol., 1963, 17, 299-313. 14) Ham, R. G. & Puck, T. P. Quantitative clonal growth of isolated mammalian cells. Methods in Enzymolopy, Academic Press Inc., London, 1962, 5, p. 90. 3) Kusano, T. & Yamane, I. General characteristics of the cells transfomred in vitro by human adenovirus type 12. Tohoku J. exp. Med., 1967, 92, 151-160. 2) Kusano, T. & Yamane, I. Transformation in. vitro of the embryonal hamster brain cells by human adenovirus type 12. Tohoku J. exp. Med., 1967, 92, 141-150. 5) Swim, H. E. & Parker, R. F. The role of carbon dioxide as an essential nutrient for six permanent strains of fibroblasts. J. biophys. biorhem. Cytol., 1958, 4, 525-528. 1) Yamane, I. & Kusano, T. In vitro transformation of cells of hamster brain by adenovirus type 12. Nature (Lond.), 1967, 213, 187-188. 15) Ham, R. G. & Puck, T. T. A regulated incubator controlling CO2 concentration, humidity and temperature for use in animal cell culture. Proc. Soc. exp. Biol. Med., 1962, 111, 67-71. 6) Gyeer, R. P. & Chang, R. S. Bicarbonate as an essential for human cells in vitro. Arch. Biochem., 1958, 73, 500-506. 11) Freeman, A. E., Hollinger, S., Price, P. J. & Calisher, C. The effect of calcium on cell lines derived from adenovirus type 12 induced tumors. Exp. Cell Res., 1965, 39, 259-264. 4) Eagle, H. Amino acid metabolism in mammalian cell culture. Science, 1959, 130, 432-437. 9) Gwatkin, R. B. L. & Simonovitch, L. Multiplication of single mammalian cells in a nonbicarbonate medium. Proc. Soc. exp. Biol. Med., 1960, 103, 718-721. 8) Chang, R. S., Liepins, H. & Margolish, M. Carbon dioxide requirement and nucleic acid metabolism of HeLa and conjunctival cells. Proc. Soc. exp. Biol. Med., 1961, 106, 149-152. 10) Kitamura, I., Van Hoosier, G., Jr., Samper, L., Taylor, G. & Trentin, J. J. Characteristics of human adenovirus type 12 induced hamster tumor cells in tissue culture. Proc. Soc. exp. Biol. Med., 1964, 116, 563-568. 7) McCoy, T. A., Maxwell, M. D. & Kruse, P. F., Jr. Carbon dioxide metabolism in the Jensen and JA sarcomas in ritro. Cancer Res., 1961, 21, 997-1000. 13) Yamane, I. & Matsuya, Y. Culture of single mammalian cells. Nature (Lond.). 1963, 199, 296. |
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Title | Alteration of Growth Rate and Nutritional Requirement of Hamster Brain Cells Transformed by Adenovirus Type 12 during Their Long-term Cultivation |
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