DNA double-strand breaks induced by very low X-ray doses are largely due to bystander effects

Radiat Res. 2008 Sep;170(3):365-71. doi: 10.1667/RR1255.1.

Abstract

Phosphorylated ATM immunofluorescence staining was used to investigate the dose-response relationship for the number of DNA double-strand breaks (DSBs) induced in primary normal human fibroblasts irradiated with doses from 1.2 to 200 mGy. The induction of DSBs showed a supralinear dose-response relationship. Radiation-induced bystander effects may explain these findings. To test this hypothesis, the number of DSBs in cells treated with lindane, an inhibitor of radiation-induced bystander effects, prior to X irradiation was assessed; a supralinear dose-response relationship was not observed. Moreover, the number of DSBs obtained by subtracting the number of phosphorylated ATM foci in lindane-treated cells from the number of phosphorylated ATM foci in untreated cells was proportional to the dose at low doses (1.2-5 mGy) and was saturated at doses from 10-200 mGy. Thus the increase in the number of DSBs in the range of 1.2-5 mGy was largely due to radiation-induced bystander effects, while at doses >10 mGy, the DSBs may be induced mainly by dose-dependent direct radiation effects and partly by dose-independent radiation-induced bystander effects. The findings in our present study provide direct evidence of the dose-response relationship for radiation-induced bystander effects from broad-beam X rays.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ataxia Telangiectasia Mutated Proteins
  • Bystander Effect / physiology*
  • Bystander Effect / radiation effects*
  • Cell Cycle Proteins / metabolism*
  • Cell Line
  • DNA / genetics*
  • DNA / radiation effects*
  • DNA Damage*
  • DNA-Binding Proteins / metabolism*
  • Dose-Response Relationship, Radiation
  • Fibroblasts / physiology*
  • Fibroblasts / radiation effects
  • Humans
  • Protein Serine-Threonine Kinases / metabolism*
  • Radiation Dosage
  • Tumor Suppressor Proteins / metabolism*
  • X-Rays

Substances

  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Tumor Suppressor Proteins
  • DNA
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • Protein Serine-Threonine Kinases