Long-term heat exposure prevents hypoxia-induced apoptosis in mouse fibroblast cells

Cell Biochem Biophys. 2014 Sep;70(1):301-7. doi: 10.1007/s12013-014-9912-9.

Abstract

Long-term continuous exposure to high ambient temperatures induces complete heat acclimation in humans and animals. However, to date, the effects of long-term exposure to heat stress on cells have not been fully evaluated. In this study, we investigated an adaptive physiological process induced in culture cells by continuous exposure to mild heat stress for 60 days. The results of this investigation provide evidence that after long-term heat acclimation in cells, (1) heat shock protein levels are increased, (2) hypoxia inducible factor-1α (HIF-1α) expression is upregulated, and (3) heat shock-induced and hypoxia-induced apoptoses are attenuated. These results suggest that the hypoxia response pathway is an intrinsic part of the heat acclimation repertoire and that the HIF-1 pathway following long-term heat acclimation induces cells with cross tolerance against hypoxia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acclimatization
  • Animals
  • Apoptosis*
  • Cell Hypoxia
  • DNA-Binding Proteins / metabolism
  • Enzyme Activation
  • Fibroblasts / cytology*
  • Fibroblasts / metabolism
  • Heat Shock Transcription Factors
  • Heat-Shock Proteins / metabolism
  • Heat-Shock Response*
  • Mice
  • NIH 3T3 Cells
  • Time Factors
  • Transcription Factors / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • DNA-Binding Proteins
  • Heat Shock Transcription Factors
  • Heat-Shock Proteins
  • Hsf1 protein, mouse
  • Transcription Factors
  • p38 Mitogen-Activated Protein Kinases