Growth kinetics rather than stress accelerate telomere shortening in cultures of human diploid fibroblasts in oxidative stress-induced premature senescence

FEBS Lett. 2001 Aug 3;502(3):109-12. doi: 10.1016/s0014-5793(01)02679-5.

Abstract

WI-38 human diploid fibroblasts underwent accelerated telomere shortening (490 bp/stress) and growth arrest after exposure to four subcytotoxic 100 microM tert-butylhydroperoxide (t-BHP) stresses, with a stress at every two population doublings (PD). After subcytotoxic 160 microM H2O2 stress or five repeated 30 microM t-BHP stresses along the same PD, respectively a 322 +/- 55 and 380 +/- 129 bp telomere shortening was observed only during the first PD after stress. The percentage of cells resuming proliferation after stress suggests this telomere shortening is due to the number of cell divisions accomplished to reach confluence during the first PD after stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Division / drug effects
  • Cell Division / physiology*
  • Cellular Senescence / physiology*
  • Diploidy
  • Fibroblasts / cytology*
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Kinetics
  • Oxidative Stress*
  • Telomere / metabolism*
  • Thymidine / chemistry
  • beta-Galactosidase / metabolism
  • tert-Butylhydroperoxide / pharmacology

Substances

  • tert-Butylhydroperoxide
  • Hydrogen Peroxide
  • beta-Galactosidase
  • Thymidine