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

Free Radic Biol Med. 1988;4(6):345-56. doi: 10.1016/0891-5849(88)90086-x.

Abstract

Further characteristics of an oxygen-tolerant variant of Chinese hamster ovary cells (CHO-99) capable of stable proliferation at 99% O2/1% CO2, and O2 level that is lethal to the parental line (CHO-20), are described. Previous work has revealed that CHO-99 cells have 2- to 4-fold increased activities of superoxide dismutases, catalase and glutathione peroxidase, and substantially increased relative volumes of mitochondria and peroxisomes. To document possible additional mechanisms of O2 tolerance we compared CHO-20 cells growing at 20% O2 (normoxia) and CHO-99 cells at 99% O2 (normobaric hyperoxia). We show the following: (1) the estimated total (oxidative and glycolytic) ATP production in CHO-99 cells was 36% decreased. ATP production through oxidative phosphorylation was 52% lower in CHO-99 cells, while the relative contribution from glycolysis was increased from 6% to 30%. The ATP content was 29% lower in CHO-99 cells, the adenylate energy charge being also significantly decreased, indicating that energy production through oxidative phosphorylation is compromised in CHO-99 cells. Cyanide-resistant respiration was 4-fold higher in CHO-99 cells, probably reflecting, at least partly, the increased peroxisomal activity in these cells. (2) The level of reduced glutathione was several fold increased in CHO-99 cells, oxidized glutathione being unaltered; (NADPH + NADP+) levels were elevated 2.7-fold, while the ratio of NADPH to NADP+ was increased almost two-fold. These changes were associated with a 50% increased metabolism of glucose through the hexose monophosphate pathway. (3) No evidence was obtained for an increased steady-state level of endogenous lipid peroxidation in CHO-99 cells, in spite of a 50% increased content of polyunsaturated fatty acids in the phospholipid fraction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology*
  • Cell Line
  • Cricetinae
  • Cricetulus
  • Cyanides / pharmacology
  • Drug Resistance
  • Energy Metabolism / drug effects*
  • Fatty Acids / analysis
  • Female
  • Glucosephosphate Dehydrogenase / metabolism
  • Glutathione / metabolism
  • Intracellular Fluid / metabolism
  • Lipid Peroxides / metabolism
  • NADP / metabolism
  • Ovary / cytology*
  • Oxygen Consumption / drug effects*
  • Pentose Phosphate Pathway / drug effects

Substances

  • Antioxidants
  • Cyanides
  • Fatty Acids
  • Lipid Peroxides
  • NADP
  • Glucosephosphate Dehydrogenase
  • Glutathione