Diverse delayed effects in human lymphoblastoid cells surviving exposure to high-LET (56)Fe particles or low-LET (137)Cs gamma radiation

• Published in: Radiation research 2001-09, Vol.156 (3), p.259-271
• Main Authors: Evans, H. H., Horng, M. F., Ricanati, M., Diaz-Insua, M., Jordan, R., Schwartz, J. L.
• Format: Article
• Language: English
• Subjects: Apoptosis; Cesium Radioisotopes; Chromosome Aberrations; Clone Cells; Humans; Iron Isotopes; Life Sciences (General); Linear Energy Transfer; Lymphocytes - enzymology; Lymphocytes - radiation effects; Mutation; Sodium-Potassium-Exchanging ATPase - genetics; Space life sciences; Thymidine Kinase - genetics
• ISSN: 0033-7587
• DOI: 10.1667/0033-7587(2001)156[0259:DDEIHL]2.0.CO;2

To obtain information on the origin of radiation-induced genomic instability, we characterized a total of 166 clones that survived exposure to (56)Fe particles or (137)Cs gamma radiation, isolated approximately 36 generations after exposure, along with their respective control clones. Cytogenetic aberrations, growth alterations, responses to a second irradiation, and mutant frequencies at the Na(+)/K(+) ATPase and thymidine kinase loci were determined. A greater percentage of clones that survived exposure to (56)Fe particles exhibited instability (defined as clones showing one or more outlying characteristics) than in the case of those that survived gamma irradiation. The phenotypes of the unstable clones that survived exposure to (56)Fe particles were also qualitatively different from those of the clones that survived gamma irradiation. A greater percentage (20%) of the unstable clones that survived gamma irradiation than those that survived exposure to (56)Fe particles (4%) showed an altered response to the second irradiation, while an increase in the percentage of clones that had an outlying frequency of ouabain-resistant and thymidine kinase mutants was more evident in the clones exposed to (56)Fe particles than in those exposed to gamma rays. Growth alterations and increases in dicentric chromosomes were found only in clones with more than one alteration. These results underscore the complex nature of genomic instability and the likelihood that radiation-induced genomic instability arises from different original events.