Possible involvement of ubiquitin function and ATP requirement in the development of thermotolerance in mammalian cells

References

• Arkinson B. G., Walden D. B. Changes in Eukaryotic Gene Expression in Response to Environmental Stress. Academic Press, London 1985
   Google Scholar
• Bond U., Schlesinger M. L. Ubiquitin is a heat shock protein in chicken embryo fibroblasts. Molecular and Cellular Biology 1985; 5: 949–956
   PubMed Web of Science ®Google Scholar
• Bond U., Schlesinger M. L. The chicken ubiquitin gene contains a heat shock promoter and express an unstable mRNA in heat-shocked cells. Molecular and Cellular Biology 1986; 12: 4601–4610
   Google Scholar
• Bond U., Agell N., Hass A. L., Redman K., Schlesinger M. J. Ubiquitin in stressed chicken embryo fibroblests. Journal of Biological Chemistry 1988; 263: 2384–2388
   PubMed Web of Science ®Google Scholar
• Boon-Niermeijer E. K., Tuyl M., van de Scheur H. Evidence for two states of thermotolerance. International Journal of Hyperthermia 1986; 2: 93–105
   PubMedGoogle Scholar
• Carlson N., Rogers S., Rechsteiner M. Microinjection of ubiquitin: changes in protein degradation in HeLa cells subjected to heat-shock. Journal of Cell Biology 1987; 104: 547–555
   PubMedGoogle Scholar
• Carlson N., Rechsteiner M. Microinjection of ubiquitin: intracellular distribution and metabolism in HeLa cells maintained under normal physiological conditions. Journal of Cell Biology 1987; 104: 537–546
   PubMedGoogle Scholar
• Ciechanover A., Heller H., Elias S., Haas A. L., Hershko A. ATP-dependent conjugation of reticulocyte proteins with the polypeptide required for protein degradation. Proceedings of the National Academy of Sciences, U.S.A. 1980; 77: 1365–1368
   PubMed Web of Science ®Google Scholar
• Ciechanover A., Finley D., Varshavsky A. Ubiquitin dependence of selective protein degradation in the mammalian cell cycle mutant ts85. Cell 1984; 37: 57–66
   PubMed Web of Science ®Google Scholar
• Finley D., Ciechanover A., Varshavsky A. Thermolability of ubiquitin-activating enzyme from mammalian cell cycle mutant ts85. Cell 1984; 37: 43–55
   PubMed Web of Science ®Google Scholar
• Finley D., Ozkaynak E., Varshavsky A. The yeast polyubiquitin gene is essential for resistance to high temperatures, starvation, and other stresses. Cell 1987; 48: 1035–1046
   PubMed Web of Science ®Google Scholar
• Gerweck L. E., Dahlberg W. K., Epstein L. F., Shimm D. S. Influence of nutrient and energy depravation on cellular response to single fractioned heat treatments. Radiation Research 1984; 99: 573–581
   PubMed Web of Science ®Google Scholar
• Haveman J., Hahn G. M. The role of energy in hypeithermia-induced mammalian cell inactivation; a study of the effects of glucose starvation and an uncoupler of oxidative phosphorylation. Journal of Cellular Physiology 1981; 197: 237–241
   Google Scholar
• Haveman J., Li G. C., Max J. Y., Kipp J. B. A. Chemically induced resistance to heat treatment and stress protein synthesis in cultured mammalian cells. International Journal of Radiation Biology 1986; 50: 51–64
   Web of Science ®Google Scholar
• Henle K. J. Thermotolerance in cultured mammalian cells. Thermotolerance Thermotolerance and Thermophily, K. J. Henle. CRC Press, Boca Raton 1987; Vol. I: 13–17
   Google Scholar
• Henle K. J., Nagle W. A., Moss A. J., Herman T. S. Cellular ATP control of heated Chinese hamster ovary cells. Radiation Research 1984; 97: 630–633
   PubMed Web of Science ®Google Scholar
• Hershko A., Eytan E., Ciechanorer A., Haas A. L. Immunochemical analysis of the turnover of ubiquitin-protein conjugates in intact cells. Relationship to the breakdown of abnormal proteins. Journal of Biological Chemistry 1982; 257: 13964–13970
   PubMedGoogle Scholar
• Landry J. Heat shock proteins and cell thermotolerance. Hyperthermia in Cancer Treatment, L. J. Anghileri, J. Robert. CRC Press, Boca Raton 1986; Vol. I: 37–58
   Google Scholar
• Landry J., Chretien P. Relationship between hyperthermia induced heat shock proteins and thermotolerance in Morris hepatoma cells. Canadian Journal of Biochemistry and Cell Biology 1983; 61: 428–437
   PubMedGoogle Scholar
• Laszlo A. Evidence of two states of thermotolerance in mammalian cells. International Journal of Hyperthermia 1988; 4: 513–526
   PubMed Web of Science ®Google Scholar
• Laval F., Michel S. Enhancement of hyperthermia-induced cytotoxicicity upon ATP deprivation. Cancer Letters 1982; 15: 61–65
   PubMed Web of Science ®Google Scholar
• Li G. C. Induction of thermotolerance and enhanced heat shock protein synthesis in Chinese hamster fibroblasts by sodium arsenite and ethanol. Journal of Cellular Physiology 1983; 122: 91–97
   Google Scholar
• Li G. C. Elevated levels of 70,000 heat shock protein in transiently thermotolerant Chinese hamster fibrodlasts and in their stable heat resistant varients. International Journal of Radiation Oncology, Biology and Physics 1985; 11: 165–177
   PubMed Web of Science ®Google Scholar
• Li G. C., Laszlo A. Thermotolerance in mammalian cells: a possible role for heat shock proteins. Changes in Eukaryotic Gene Expression in Response to Environmental Stress, B. G. Atkinson, D. B. Walden. Academic Press, New York 1985; 227–254
   Google Scholar
• Lindquist S. The heat shock response. Annual Reviews of Biochemistry 1986; 55: 1151–1191
   PubMed Web of Science ®Google Scholar
• Matsumoto Y., Yasuda H., Marunouchi T., Yamada M. Decrease in uH2A (protein A24) of a mouse temperature-sensitive mutant. FEBS Letters 1983; 151: 139–142
   PubMed Web of Science ®Google Scholar
• Mita S., Yasuda H., Marunouchi T., Ishiko S., Yamada M. A temperature-sensitive mutant of cultured mouse cells defective in chromosomal condensation. Experimental Cell Research 1980; 126: 407–416
   PubMed Web of Science ®Google Scholar
• Mizuno S., Ohkawara A., Suzuki K. Defect in the development of thermotolerance in the mouse temperature-sensitive mutant ts85 lacking ubiquitin-activating enzyme. Japanesse Journal of Cancer Research, (Gann) 1988; 79: 17–20
   PubMedGoogle 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: 105–113
   PubMed Web of Science ®Google Scholar
• Parag H., Raboy B., Kulka R. G. Effect of heat shock on protein degradation in mammalian cells: involvement of the ubiquitin system. EMBO Journal 1987; 6: 55–61
   PubMed Web of Science ®Google Scholar
• Pryzybytkowski E., Bates J. 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
• Raboy B., Parag H. A., Kulka R. G. Conjugation of [125I] ubiquitin to cellular proteins in permeabilized mammalian cells: comparison of mitotic and interphase cells. EMBO Journal 1986; 5: 863–869
   PubMedGoogle Scholar
• Rechsteiner M. Ubiquitin-mediated pathway for intracellular proteolysis. Annual Reviews of Cell Biology 1987; 3: 1–30
   PubMedGoogle Scholar
• Schlesinger M. J. Heat shock proteins; the search for functions. Journal of Cell Biology 1986; 103: 321–325
   PubMed Web of Science ®Google Scholar
• Shinohara K., Kawakami N., Kugotani M., Nakano H. Gallium citrate, a new sensitizer of cells to hyperthermia. Japanese Journal of Cancer Research (Gann) 1988; 79: 21–23
   PubMedGoogle Scholar
• Tanaka K., Yoshioka A S., Tanaka S., Wataya Y. An improved method for the quantitative determination of deoxyribonucleoside triphosphates in cell extract. Analytical Biochemistry 1984; 139: 35–41
   PubMed Web of Science ®Google Scholar
• Tomasovic S. P., Steck P. A., Heitzman D. Heat-stress proteins and thermal resistance in rat mammary tumor cells. Radiation Research 1983; 95: 399–413
   PubMed Web of Science ®Google Scholar
• Tsai Y-J., Hanaoka F., Nakano M. M., Yasmada M. A mammalian DNA—mutant decreasing nuclear DNA polymerase α activity at nonpermissive temperature. Biochemical and Biophysical Research Communications 1979; 91: 1190–1195
   PubMedGoogle Scholar
• Watson K., Dunlop G., Cavicchiou R. R. Mitochondrial and cytoplasmic protein syntheses are not required for heat shock acquisition of ethanol and thermotolerance in yeast. FEBS Letters 1984; 172: 299–302
   PubMed Web of Science ®Google Scholar
• Widelitz R. B., Magun B. E., Gerner E. W. Effects of cycloheximide on thermotolerance expression, heat shock protein synthesis and heat shock protein mRNA accumulation in rat fibroblasts. Molecular and Cellular Biology 1986; 6: 1088–1094
   PubMed Web of Science ®Google Scholar
• Yasuda H., Matsumoto Y., Mita S., Marunouchi T., Yamada M. A mouse temperature-sensitive mutant defective in HI histone phosphorylation is defective in deoxyribonucleic acid synthesis and chromosome condensation. Biochemistry 1981; 20: 4414–4419
   PubMed Web of Science ®Google Scholar
• Yasumitsu H., Hanaoka F., Yasuda H., Murakami Y., Enomoto T., Yamada M. Isolation and initial characterization of a temperature-sensitive mutant of mouse FM3A cells defective in cytokinesis. Cell Structure and Function 1985; 10: 79–88
   PubMedGoogle Scholar