Involvement of protein synthesis in the development of thermotolerance using a CHO temperature-sensitive mutant

References

• Anderson K. M., Baranowski J. Nuclear protein synthesis in a temperature-sensitive Chinese hamster ovary cell line at 40°C. Clinical Physiology and Biochemistry 1984; 2: 304–319
   PubMedGoogle Scholar
• Anderson K. M., Bass B., Riberstein M., Saclarides T. Nuclear protein synthesis at permissive and non-permissive temperature in CHO with a temperature sensitive defect in cytoplasmic non-mitochondrial protein synthesis. Experimental Cell Research 1979; 121: 191–207
   PubMedGoogle Scholar
• Elder P. K., Schmidt L. J., Ono T., Getz M. J. Specific stimulation of actin gene transcription by epidermal growth factor and cycloheximide. Proceedings of the National Academy of Sciences, U.S.A. 1984; 81: 7476–7480
   PubMed Web of Science ®Google Scholar
• Freeman M. L., Scidmore N. C., Meredith M. J. Inhibition of heat shock protein synthesis and thermotolerance by cycloheximide. Radiation Research 1987; 112: 564–574
   PubMed Web of Science ®Google Scholar
• Hallberg R. L. No heat shock protein synthesis is required for induced thermostabilization of translational machinery. Molecular and Cellular Biology 1986; 6: 1088–1094
   PubMedGoogle Scholar
• Harvey W. F., Bedford J. S. Isolation and characterization of heat sensitive, thermotolerant defective mutants of CHO cells. Radiation Research 1988; 113: 526–542
   PubMed Web of Science ®Google Scholar
• Henle K. J., Leeper D. B. Modification of heat response and thermotolerance by cycloheximide, hydroxyurea, lucanthone in CHO cells. Radiation Research 1982; 90: 339–347
   PubMed Web of Science ®Google Scholar
• Henle K. J., Karamuz J. E., Leeper D. B. Induction of thermotolerance in heat fractionation and Chinese hamster ovary cells by high (45°) and low (40°) hyperthermia. Cancer Research 1978; 38: 570–574
   PubMed Web of Science ®Google Scholar
• Henle K. J., Nagee W. A., Norris J. S., Moss J. A. Enhanced glycosylation of a 50 kd protein during development of thermotolerance in CHO cells. International Journal of Radiation Biology 1988; 53(5)839–847
   Web of Science ®Google Scholar
• Highfield D. P., Dewey W. C. Inhibition of DNA synthesis in synchronous Chinese Hamster cells treated in G1 and early S phase with cycloheximide or puromycin. Experimental Cell Research 1972; 74: 314–320
   Google Scholar
• Jomain-Baum M., Hanson R. W. The inhibition by cycloheximide of lipid metabolism by rat adipose tissue in vitro. Life Sciences, 16: 345–352
   PubMedGoogle Scholar
• Kalckar H. M., Ullrey D. B., Laursen R. A. Effects of combined glutamine and serum deprivation on glucose control of hexose transport in mammalian fibroblast cultures. Proceedings of the National Academy of Sciences, U.S.A. 1980; 77: 5958–5961
   PubMedGoogle Scholar
• Kraus K. W., Hallberg E. M., Hallberg R. Characterization of a Tetrahymena thermophila mutant strain unable to develop normal thermotolerance. Molecular and Cellular Biology 1986; 6: 3854–3861
   PubMedGoogle Scholar
• Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature (London) 1970; 227: 680–685
   PubMed Web of Science ®Google Scholar
• Laskey R. A., Mills A. D. Quantitative film detection of tritium and 14C in polyacrylamide gels by fluorography. European Journal of Biochemistry 1975; 56: 335–341
   PubMedGoogle Scholar
• Lee Y. J., Dewey W. C. Protection of Chinese hamster ovary cells from hyperthermic killing by cycloheximide or puromycin. Radiation Research 1986; 106: 98–110
   PubMed Web of Science ®Google Scholar
• Li G., Werb Z. Correlation between synthesis of heat shock proteins and development of thermotolerance in Chinese hamster fibroblasts. Proceedings of the National Academy of Sciences, U.S.A. 1982; 79: 3218–3222
   PubMed Web of Science ®Google Scholar
• Martin T. F. J. Paradoxical effects of protein synthesis inhibitors on uridine uptake in cultured cells: Possible role of uncharged tRNA in regulatory metabolism. Journal of Cell Physiology 1980; 103: 489–502
   PubMedGoogle Scholar
• McKenzie S. L., Henkoff S., Meselson M. Localization of RNA from heat induced polysomes at puff sites in D. melanogaster. Proceedings of the National Academy of Sciences, U.S.A. 1975; 72: 1117–1121
   PubMed Web of Science ®Google Scholar
• Mizuno S., Ohkawara A., Suzuki K. Defect in the development of thermotolerance and enhanced heat shock protein synthesis in the mouse temperature-sensitive mutant ts85 cells upon moderate hyperthermia. International Journal of Hyperthermia 1989; 5(1)105–113
   PubMed Web of Science ®Google Scholar
• Murnane J. P., Li G. C. Effects of heat shock on the intracellular distribution of proteins. Radiation Research 1985; 101: 480–490
   PubMed Web of Science ®Google Scholar
• Nover L. Heat Shock Response of Eukaryotic Cells. Springer-Verlag, Berlin 1984
   Google Scholar
• Petersen N., Mitchell H. K. Recovery of protein synthesis following heat shock; preheat treatment affects mRNA translation. Proceedings of the National Academy of Sciences, U.S.A. 1981; 78: 1708–1711
   PubMed Web of Science ®Google Scholar
• Przybytkowski E. J., Bates H. T., Bates D. A., MacKillop W. J. Thermal adaptation in CHO cells at 40°C: the influence of growth conditions and the role of heat shock proteins. Radiation Research 1986; 107: 317–331
   PubMedGoogle Scholar
• Reiter T., Penman S. ‘Prompt’ hsps: translationally regulated synthesis of new proteins associated with the nuclear matrix-intermediate filaments as an early response to heat shock. Proceedings of the National Academy of Sciences, U.S.A. 1983; 80: 4737–4741
   PubMed Web of Science ®Google Scholar
• Riabowol K. T., Mizzen L. A., Welch W. J. Heat shock is lethal to fibroblasts microinjected with antibodies against hsp70. Science 1988; 242: 433–436
   PubMed Web of Science ®Google Scholar
• Thompson L. H., Harkins J. L., Stanners C. P. A mammalian cell mutant with a temperature-sensitive leucyl transfer RNA synthetase. Proceedings of the National Academy of Sciences, U.S.A. 1973; 70: 3094–3098
   PubMedGoogle Scholar
• Yatvin M. B., Clark A. W., Siegel F. Major E. coli heat stress protein do not translocate: implications for cell survival. International Journal of Radiation Biology 1987; 52(4)603–613
   Google Scholar
• Yezzi M. J., Blakeley E. A., Tobias C. A. Split-dose recovery and protein synthesis in X-irradiated CHO cells. Radiation Research 1988; 114: 281–296
   PubMedGoogle Scholar