Cytotoxic and Mutagenic Effects of Chronic Low-Dose-Rate Irradiation on TERT-Immortalized Human Cells

Nakamura, H., Fukami, H., Hayashi, Y., Tachibana, A., Nakatsugawa, S., Hamaguchi, M. and Ishizaki, K. Cytotoxic and Mutagenic Effects of Chronic Low-Dose-Rate Irradiation on TERT-Immortalized Human Cells. Radiat. Res. 163, 283– 288 (2005). To analyze the genetic effects of low-dose-rate radiation on...

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Veröffentlicht in:Radiation research 2005-03, Vol.163 (3), p.283-288
Hauptverfasser: Nakamura, Hideaki, Fukami, Hiroko, Hayashi, Yuko, Tachibana, Akira, Nakatsugawa, Shigekazu, Hamaguchi, Michinari, Ishizaki, Kanji
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container_end_page 288
container_issue 3
container_start_page 283
container_title Radiation research
container_volume 163
creator Nakamura, Hideaki
Fukami, Hiroko
Hayashi, Yuko
Tachibana, Akira
Nakatsugawa, Shigekazu
Hamaguchi, Michinari
Ishizaki, Kanji
description Nakamura, H., Fukami, H., Hayashi, Y., Tachibana, A., Nakatsugawa, S., Hamaguchi, M. and Ishizaki, K. Cytotoxic and Mutagenic Effects of Chronic Low-Dose-Rate Irradiation on TERT-Immortalized Human Cells. Radiat. Res. 163, 283– 288 (2005). To analyze the genetic effects of low-dose-rate radiation on human cells, we used human telomere reverse transcriptase (TERT)-immortalized fibroblast cells obtained from normal individuals. We studied the effect of low-dose-rate (0.3 mGy/ min) and high-dose-rate (2 Gy/min) radiation on cells in a confluent state. Survival and micronucleus induction frequency showed higher resistance after irradiation at low dose rate than at high dose rate. The survival after 5 Gy of high-dose-rate radiation was 0.01 compared to 0.3 after low-dose-rate irradiation at the same dose. In accordance with this, the level of HPRT mutation induction by low-dose-rate radiation decreased to approximately one-eighth that for high-dose-rate radiation. We then characterized the mutants by multiplex PCR analysis, which showed that the fraction of deletion mutations was lower in the mutant cells induced at low dose rate than at high dose rate. Furthermore, the size of the deletions in mutant cells induced by low-dose-rate radiation appeared to be smaller than those in mutant cells irradiated at high dose rate. Only a few exons were deleted in the former mutants while all exons were deleted in most of the latter mutants. The present study indicates that the genetic effects of low-dose-rate radiation on nonproliferating normal human cells are quantitatively and qualitatively less severe than the effect of high-dose-rate radiation.
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Cytotoxic and Mutagenic Effects of Chronic Low-Dose-Rate Irradiation on TERT-Immortalized Human Cells. Radiat. Res. 163, 283– 288 (2005). To analyze the genetic effects of low-dose-rate radiation on human cells, we used human telomere reverse transcriptase (TERT)-immortalized fibroblast cells obtained from normal individuals. We studied the effect of low-dose-rate (0.3 mGy/ min) and high-dose-rate (2 Gy/min) radiation on cells in a confluent state. Survival and micronucleus induction frequency showed higher resistance after irradiation at low dose rate than at high dose rate. The survival after 5 Gy of high-dose-rate radiation was 0.01 compared to 0.3 after low-dose-rate irradiation at the same dose. In accordance with this, the level of HPRT mutation induction by low-dose-rate radiation decreased to approximately one-eighth that for high-dose-rate radiation. We then characterized the mutants by multiplex PCR analysis, which showed that the fraction of deletion mutations was lower in the mutant cells induced at low dose rate than at high dose rate. Furthermore, the size of the deletions in mutant cells induced by low-dose-rate radiation appeared to be smaller than those in mutant cells irradiated at high dose rate. Only a few exons were deleted in the former mutants while all exons were deleted in most of the latter mutants. 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Cytotoxic and Mutagenic Effects of Chronic Low-Dose-Rate Irradiation on TERT-Immortalized Human Cells. Radiat. Res. 163, 283– 288 (2005). To analyze the genetic effects of low-dose-rate radiation on human cells, we used human telomere reverse transcriptase (TERT)-immortalized fibroblast cells obtained from normal individuals. We studied the effect of low-dose-rate (0.3 mGy/ min) and high-dose-rate (2 Gy/min) radiation on cells in a confluent state. Survival and micronucleus induction frequency showed higher resistance after irradiation at low dose rate than at high dose rate. The survival after 5 Gy of high-dose-rate radiation was 0.01 compared to 0.3 after low-dose-rate irradiation at the same dose. In accordance with this, the level of HPRT mutation induction by low-dose-rate radiation decreased to approximately one-eighth that for high-dose-rate radiation. We then characterized the mutants by multiplex PCR analysis, which showed that the fraction of deletion mutations was lower in the mutant cells induced at low dose rate than at high dose rate. Furthermore, the size of the deletions in mutant cells induced by low-dose-rate radiation appeared to be smaller than those in mutant cells irradiated at high dose rate. Only a few exons were deleted in the former mutants while all exons were deleted in most of the latter mutants. 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Cytotoxic and Mutagenic Effects of Chronic Low-Dose-Rate Irradiation on TERT-Immortalized Human Cells. Radiat. Res. 163, 283– 288 (2005). To analyze the genetic effects of low-dose-rate radiation on human cells, we used human telomere reverse transcriptase (TERT)-immortalized fibroblast cells obtained from normal individuals. We studied the effect of low-dose-rate (0.3 mGy/ min) and high-dose-rate (2 Gy/min) radiation on cells in a confluent state. Survival and micronucleus induction frequency showed higher resistance after irradiation at low dose rate than at high dose rate. The survival after 5 Gy of high-dose-rate radiation was 0.01 compared to 0.3 after low-dose-rate irradiation at the same dose. In accordance with this, the level of HPRT mutation induction by low-dose-rate radiation decreased to approximately one-eighth that for high-dose-rate radiation. We then characterized the mutants by multiplex PCR analysis, which showed that the fraction of deletion mutations was lower in the mutant cells induced at low dose rate than at high dose rate. Furthermore, the size of the deletions in mutant cells induced by low-dose-rate radiation appeared to be smaller than those in mutant cells irradiated at high dose rate. Only a few exons were deleted in the former mutants while all exons were deleted in most of the latter mutants. The present study indicates that the genetic effects of low-dose-rate radiation on nonproliferating normal human cells are quantitatively and qualitatively less severe than the effect of high-dose-rate radiation.</abstract><cop>United States</cop><pub>Radiation Research Society</pub><pmid>15733035</pmid><doi>10.1667/RR3310</doi><tpages>6</tpages></addata></record>
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subjects Cell lines
Cell Survival - radiation effects
Chromosome Aberrations
Cultured cells
DNA damage
DNA-Binding Proteins
Dose-Response Relationship, Radiation
Exons
Fibroblasts
Fibroblasts - metabolism
Gene Deletion
Genetic mutation
Humans
Hypoxanthine Phosphoribosyltransferase - genetics
Irradiation
Male
Micronucleus Tests
Mutagens
Mutation
Polymerase Chain Reaction
Radiation damage
Radiation dosage
Regression Analysis
REGULAR ARTICLES
Somatic cells
Telomerase - metabolism
title Cytotoxic and Mutagenic Effects of Chronic Low-Dose-Rate Irradiation on TERT-Immortalized Human Cells
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