Literature DB >> 15447047

Persistence of chromatid aberrations in the cells of solid mouse tissues exposed to 137Cs gamma radiation.

Mitchell S Turker1, Jeffrey L Schwartz, Robert Jordan, Olga N Ponomareva, Lanelle Connolly, Elizabeth Kasameyer, Michael Lasarev, Lisa Clepper.   

Abstract

Primary mouse ear and kidney cultures were established for determination of cytogenetic aberrations at short (3 days to 1 month) and long (12-23 months) times after exposure of their right sides to 7.5 Gy of (137)Cs gamma radiation. In every case, higher levels of aberrations were observed in primary cultures established from the irradiated tissues than in those established from the contralateral tissues. The most common aberrations in the contralateral tissues and those from nonirradiated mice were chromatid and isochromatid breaks and small chromatid fragments. Primary cells from irradiated tissues removed from animals within a month of exposure displayed a variety of unstable chromosome-type aberrations characteristic of recent exposure to ionizing radiation including rings, dicentrics, double minutes, and large acentric fragments. The percentages of cells exhibiting chromatid breaks and small chromatid fragments were also markedly elevated. Although the levels of chromosome-type aberrations found in primary cells from irradiated tissues dropped to near background levels a year or more after exposure, chromatid-type aberrations remained elevated. These results are consistent with long-term persistence of damage in the genomes of ionizing radiation-exposed cells in solid tissues and the induction of genomic instability in vivo.

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Year:  2004        PMID: 15447047     DOI: 10.1667/rr3240

Source DB:  PubMed          Journal:  Radiat Res        ISSN: 0033-7587            Impact factor:   2.841


  2 in total

1.  Cytogenetic effects of low-dose radiation with different LET in human peripheral blood lymphocytes.

Authors:  E A Nasonova; N L Shmakova; O V Komova; L A Mel'nikova; T A Fadeeva; E A Krasavin; S Ritter
Journal:  Radiat Environ Biophys       Date:  2006-10-10       Impact factor: 1.925

2.  Marked aneuploidy and loss of multiple chromosomes are common in autosomal mutants isolated from normal mouse kidney epithelium.

Authors:  Cristian Dan; Dmytro Grygoryev; Kelly Sandfort; Marissa Connolly; Brittany Cross; Michael Lasarev; Amy Kronenberg; Mitchell S Turker
Journal:  Genes Chromosomes Cancer       Date:  2011-01-19       Impact factor: 5.006

  2 in total

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