Variation in mitochondrial function in hypoxia-sensitive and hypoxia-tolerant human glioma cells

Br J Cancer. 2002 Feb 12;86(4):619-24. doi: 10.1038/sj.bjc.6600087.

Abstract

We have shown previously that human glioblastoma multiforme cells vary in their ability to survive under hypoxic conditions. Under oxygen limiting conditions, hypoxia-tolerant cells decrease their oxygen consumption rate whereas hypoxia-sensitive cells continue to consume oxygen at a relatively steady rate until the oxygen supply becomes exhausted. We now show that hypoxia-tolerant and hypoxia-sensitive cells exhibit distinct patterns of mitochondrial function in response to hypoxic challenge. Hypoxia-tolerant cell lines retain stable mitochondrial membrane potential and ATP concentration when incubated under oxygen limiting conditions. In addition, hypoxia-tolerant cell lines are consistently more sensitive to a wide spectrum of inhibitors of mitochondrial function than are hypoxia-sensitive cells. In contrast, the hypoxia-sensitive cells are unable to maintain stable mitochondrial membrane potential and ATP levels when incubated at reduced oxygen tension. These results demonstrate significant differences in the mitochondrial function between these two phenotypes and reinforce previous data that suggest a regulatory role for mitochondria in the development of hypoxia tolerance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Brain Neoplasms / metabolism*
  • Cell Hypoxia
  • Cell Membrane / metabolism
  • Cell Survival
  • Flow Cytometry
  • Formazans
  • Gene Expression Regulation
  • Glioma / metabolism*
  • Humans
  • Hypoxia / metabolism*
  • Ion Channels
  • Membrane Potentials
  • Mitochondria / metabolism*
  • Oxygen / metabolism
  • Sensitivity and Specificity
  • Tetrazolium Salts
  • Tumor Cells, Cultured
  • Uncoupling Agents / metabolism

Substances

  • Formazans
  • Ion Channels
  • Tetrazolium Salts
  • Uncoupling Agents
  • MTT formazan
  • Adenosine Triphosphate
  • Oxygen