The relative biological effectiveness of densely ionizing heavy-ion radiation for inducing ocular cataracts in wild type versus mice heterozygous for the ATM gene

Radiat Environ Biophys. 2006 Jul;45(2):99-104. doi: 10.1007/s00411-006-0052-5. Epub 2006 Jun 24.

Abstract

The accelerated appearance of ocular cataracts at younger ages has been recorded in both astronauts and airline pilots, and is usually attributed to high-energy heavy ions in galactic cosmic ray radiation. We have previously shown that high-LET 1-GeV/nucleon (56)Fe ions are significantly more effective than X-rays in producing cataracts in mice. We have also shown that mice haploinsufficient for ATM develop cataracts earlier than wild-type animals, when exposed to either low-LET X-rays or high-LET (56)Fe ions. In this paper we derive quantitative estimates for the relative biological effectiveness (RBE) of high energy (56)Fe ions compared with X-rays, both for wild type and for mice haploinsufficient for ATM. There is a clear trend toward higher RBE's in haploinsufficient animals, both for low- and high-grade cataracts. Haploinsufficiency for ATM results in an enhanced sensitivity to X-rays compared with the wild type, and this enhancement appears even larger after exposure to high-LET heavy ions.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Ataxia Telangiectasia Mutated Proteins
  • Cataract / etiology
  • Cataract / genetics*
  • Cell Cycle Proteins / genetics*
  • DNA-Binding Proteins / genetics*
  • Heavy Ions*
  • Heterozygote
  • Iron*
  • Linear Energy Transfer
  • Mice
  • Mice, Knockout
  • Protein Serine-Threonine Kinases / genetics*
  • Radiation Dosage
  • Radiation Injuries, Experimental / etiology
  • Radiation Injuries, Experimental / genetics*
  • Relative Biological Effectiveness
  • Time Factors
  • Tumor Suppressor Proteins / genetics*
  • X-Rays*

Substances

  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Tumor Suppressor Proteins
  • Iron
  • Ataxia Telangiectasia Mutated Proteins
  • Atm protein, mouse
  • Protein Serine-Threonine Kinases