Induction of the glucose-6-phosphate dehydrogenase gene expression by chronic hypoxia in PC12 cells

FEBS Lett. 2004 Jul 2;569(1-3):256-60. doi: 10.1016/j.febslet.2004.06.004.

Abstract

We studied the regulation of glucose-6-phosphate dehydrogenase (G6PD) gene expression by chronic hypoxia. G6PD mRNA level and activity were increased in PC12 cells by hypoxia in a dose- and time-dependent manner. Cobalt chloride and dimethyloxalylglycine, which can mimic hypoxia, also activated G6PD gene expression. Interestingly, hypoxia-induced G6PD expression followed a time course much slower than that of phosphoglycerate kinase 1 (PGK1), a hypoxia-inducible factor (HIF)-dependent glycolytic enzyme. Hypoxic-G6PD induction was almost negligible in non-excitable Buffalo rat liver cells, although in these cells PGK1 was strongly upregulated by low PO(2). Furthermore, G6PD but not PGK1 induction was blocked by the antioxidants glutathione and N-acetylcysteine. These results suggest the dependence of G6PD gene expression on HIF and intracellular redox status and the differential hypoxic regulation of glucose-metabolizing enzymes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cell Hypoxia / physiology*
  • Cobalt / pharmacology
  • DNA Primers
  • Gene Expression Regulation, Enzymologic / genetics*
  • Gene Expression Regulation, Neoplastic / genetics*
  • Glucosephosphate Dehydrogenase / genetics*
  • Kinetics
  • PC12 Cells
  • Polymerase Chain Reaction
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / isolation & purification
  • Rats

Substances

  • DNA Primers
  • RNA, Neoplasm
  • Cobalt
  • Glucosephosphate Dehydrogenase
  • cobaltous chloride