Characterization of oxygen-tolerant Chinese hamster ovary cells: II. Energy metabolism and antioxidant status

作者: P. van der Valk , J.J.P. Gille , L.H.W. van der Plas , J.F. Jongkind , A. Verkerk

DOI: 10.1016/0891-5849(88)90086-X

关键词: GlutathioneBiochemistryOxidative phosphorylationChinese hamster ovary cellAdenylate kinasePentose phosphate pathwayMetabolismGlutathione peroxidaseBiologyEnergy charge

摘要: Abstract Further characteristics of an oxygen-tolerant variant Chinese hamster ovary cells (CHO-99) capable stable proliferation at 99% O 2 /1% CO , level that is lethal to the parental line (CHO-20), are described. Previous work has revealed CHO-99 have 2- 4-fold increased activities superoxide dismutases, catalase and glutathione peroxidase, substantially relative volumes mitochondria peroxisomes. To document possible additional mechanisms tolerance we compared CHO-20 growing 20% (normoxia) (normobaric hyperoxia). We show following: (1) estimated total (oxidative glycolytic) ATP production in was 36% decreased. through oxidative phosphorylation 52% lower cells, while contribution from glycolysis 6% 30%. The content 29% adenylate energy charge being also significantly decreased, indicating compromised cells. Cyanide-resistant respiration higher probably reflecting, least partly, peroxisomal activity these (2) reduced several fold oxidized unaltered; (NADPH + NADP ) levels were elevated 2.7-fold, ratio NADPH almost two-fold. These changes associated with a 50% metabolism glucose hexose monophosphate pathway. (3) No evidence obtained for steady-state endogenous lipid peroxidation spite polyunsaturated fatty acids phospholipid fraction.

参考文章(45)
L.J. Reitzer, B.M. Wice, D. Kennell, The pentose cycle. Control and essential function in HeLa cell nucleic acid synthesis. Journal of Biological Chemistry. ,vol. 255, pp. 5616- 5626 ,(1980) , 10.1016/S0021-9258(19)70674-7
Gyula B. Kovachich, Niels Haugaard, Biochemical Aspects of Oxygen Toxicity in the Metazoa Springer, New York, NY. pp. 210- 234 ,(1981) , 10.1007/978-1-4612-5890-2_11
B M Wice, L J Reitzer, D Kennell, Evidence that glutamine, not sugar, is the major energy source for cultured HeLa cells. Journal of Biological Chemistry. ,vol. 254, pp. 2669- 2676 ,(1979) , 10.1016/S0021-9258(17)30124-2
J D Crapo, B A Freeman, Biology of disease: free radicals and tissue injury. Laboratory Investigation. ,vol. 47, pp. 412- 426 ,(1982)
Roland R. Rueckert, Gerald C. Mueller, Effect of oxygen tension on HeLa cell growth. Cancer Research. ,vol. 20, pp. 944- 949 ,(1960)
B.A. Freeman, J.D. Crapo, Hyperoxia increases oxygen radical production in rat lungs and lung mitochondria. Journal of Biological Chemistry. ,vol. 256, pp. 10986- 10992 ,(1981) , 10.1016/S0021-9258(19)68544-3
John A. Buege, Steven D. Aust, Microsomal lipid peroxidation. Methods in Enzymology. ,vol. 52, pp. 302- 310 ,(1978) , 10.1016/S0076-6879(78)52032-6
L C McDonald, C R Hackney, B Ray, Enhanced recovery of injured Escherichia coli by compounds that degrade hydrogen peroxide or block its formation. Applied and Environmental Microbiology. ,vol. 45, pp. 360- 365 ,(1983) , 10.1128/AEM.45.2.360-365.1983
Donald F. Tierney, Mohammad G. Mustafa, Biochemical and Metabolic Changes in the Lung with Oxygen, Ozone, and Nitrogen Dioxide Toxicity1, 2 The American review of respiratory disease. ,vol. 118, pp. 1061- ,(2015) , 10.1164/ARRD.1978.118.6.1061
R. E. Kimura, G. E. Thulin, D. Wender, J. B. Warshaw, Decreased oxidative metabolism in neonatal rat lung exposed to hyperoxia Journal of Applied Physiology. ,vol. 55, pp. 1501- 1505 ,(1983) , 10.1152/JAPPL.1983.55.5.1501