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The in vivo Pig-a gene mutation assay is useful for evaluating the genotoxicity of ionizing radiation in mice
The in vivo Pig‐a mutation assay has been adapted for measuring mutation in rats, mice, monkeys, and humans. To date, the assay has been used mainly to assess the mutagenicity of chemicals that are known to be powerful point mutagens. The assay has not been used to measure the biological effects ass...
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Published in: | Environmental and molecular mutagenesis 2012-10, Vol.53 (8), p.579-588 |
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description | The in vivo Pig‐a mutation assay has been adapted for measuring mutation in rats, mice, monkeys, and humans. To date, the assay has been used mainly to assess the mutagenicity of chemicals that are known to be powerful point mutagens. The assay has not been used to measure the biological effects associated with ionizing radiation. In this study, we modified the Pig‐a gene mutation assay (Kimoto et al. [2011b]: Mutat Res 723:36‐42) and used 3‐color staining with fluorescently labeled anti‐CD24, anti‐TER‐119, and anti‐CD71 to detect the Pig‐a mutant frequencies in total red blood cells (RBCs) and in reticulocytes (RETs) from X‐irradiated mice. Single exposures to X‐irradiation resulted in dose‐ and time‐dependent increases in Pig‐a mutant frequencies, and these subsequently declined over time returning to background frequencies. The same total amount of radiation, delivered either as a single dose or as four repeat doses at weekly intervals, increased Pig‐a mutant frequencies to comparable levels, reaching maxima 2–3 weeks after the single dose or 2–3 weeks after the last of the repeat doses. These increased frequencies subsequently returned to background levels. Our results indicated that the 3‐color Pig‐a assay was useful for evaluating the in vivo genotoxicity of radiation. Environ. Mol. Mutagen., 2012. © 2012 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/em.21724 |
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To date, the assay has been used mainly to assess the mutagenicity of chemicals that are known to be powerful point mutagens. The assay has not been used to measure the biological effects associated with ionizing radiation. In this study, we modified the Pig‐a gene mutation assay (Kimoto et al. [2011b]: Mutat Res 723:36‐42) and used 3‐color staining with fluorescently labeled anti‐CD24, anti‐TER‐119, and anti‐CD71 to detect the Pig‐a mutant frequencies in total red blood cells (RBCs) and in reticulocytes (RETs) from X‐irradiated mice. Single exposures to X‐irradiation resulted in dose‐ and time‐dependent increases in Pig‐a mutant frequencies, and these subsequently declined over time returning to background frequencies. The same total amount of radiation, delivered either as a single dose or as four repeat doses at weekly intervals, increased Pig‐a mutant frequencies to comparable levels, reaching maxima 2–3 weeks after the single dose or 2–3 weeks after the last of the repeat doses. These increased frequencies subsequently returned to background levels. Our results indicated that the 3‐color Pig‐a assay was useful for evaluating the in vivo genotoxicity of radiation. Environ. Mol. Mutagen., 2012. © 2012 Wiley Periodicals, Inc.</description><identifier>ISSN: 0893-6692</identifier><identifier>EISSN: 1098-2280</identifier><identifier>DOI: 10.1002/em.21724</identifier><identifier>PMID: 22911630</identifier><identifier>CODEN: EMMUEG</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Biological and medical sciences ; Cells, Cultured ; Erythrocytes - metabolism ; Erythrocytes - radiation effects ; Flow Cytometry ; Fundamental and applied biological sciences. Psychology ; Genetics of eukaryotes. Biological and molecular evolution ; genotoxicity ; Male ; Medical sciences ; Mice ; Mice, Inbred C57BL ; Mutagenicity Tests ; Mutation - genetics ; Pig-a mutant frequency ; Radiation, Ionizing ; red blood cells ; reticulocytes ; Reticulocytes - metabolism ; Reticulocytes - radiation effects ; Toxicology ; X-irradiation</subject><ispartof>Environmental and molecular mutagenesis, 2012-10, Vol.53 (8), p.579-588</ispartof><rights>Copyright © 2012 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4554-d706e98912fee5abdcb1705b19913a2c65675d2e36725995742a3765663603623</citedby><cites>FETCH-LOGICAL-c4554-d706e98912fee5abdcb1705b19913a2c65675d2e36725995742a3765663603623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26568782$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22911630$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ohtani, Shin</creatorcontrib><creatorcontrib>Unno, Aiko</creatorcontrib><creatorcontrib>Ushiyama, Akira</creatorcontrib><creatorcontrib>Kimoto, Takafumi</creatorcontrib><creatorcontrib>Miura, Daishiro</creatorcontrib><creatorcontrib>Kunugita, Naoki</creatorcontrib><title>The in vivo Pig-a gene mutation assay is useful for evaluating the genotoxicity of ionizing radiation in mice</title><title>Environmental and molecular mutagenesis</title><addtitle>Environ. Mol. Mutagen</addtitle><description>The in vivo Pig‐a mutation assay has been adapted for measuring mutation in rats, mice, monkeys, and humans. To date, the assay has been used mainly to assess the mutagenicity of chemicals that are known to be powerful point mutagens. The assay has not been used to measure the biological effects associated with ionizing radiation. In this study, we modified the Pig‐a gene mutation assay (Kimoto et al. [2011b]: Mutat Res 723:36‐42) and used 3‐color staining with fluorescently labeled anti‐CD24, anti‐TER‐119, and anti‐CD71 to detect the Pig‐a mutant frequencies in total red blood cells (RBCs) and in reticulocytes (RETs) from X‐irradiated mice. Single exposures to X‐irradiation resulted in dose‐ and time‐dependent increases in Pig‐a mutant frequencies, and these subsequently declined over time returning to background frequencies. The same total amount of radiation, delivered either as a single dose or as four repeat doses at weekly intervals, increased Pig‐a mutant frequencies to comparable levels, reaching maxima 2–3 weeks after the single dose or 2–3 weeks after the last of the repeat doses. These increased frequencies subsequently returned to background levels. Our results indicated that the 3‐color Pig‐a assay was useful for evaluating the in vivo genotoxicity of radiation. Environ. Mol. Mutagen., 2012. © 2012 Wiley Periodicals, Inc.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>Erythrocytes - metabolism</subject><subject>Erythrocytes - radiation effects</subject><subject>Flow Cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>genotoxicity</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mutagenicity Tests</subject><subject>Mutation - genetics</subject><subject>Pig-a mutant frequency</subject><subject>Radiation, Ionizing</subject><subject>red blood cells</subject><subject>reticulocytes</subject><subject>Reticulocytes - metabolism</subject><subject>Reticulocytes - radiation effects</subject><subject>Toxicology</subject><subject>X-irradiation</subject><issn>0893-6692</issn><issn>1098-2280</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LAzEQhoMoWqvgL5BcBC9b87FJNkeRWoVWPSiCl5Duztbofshmt7r-elNb9eRpYOZ554EXoSNKRpQQdgbliFHF4i00oEQnEWMJ2UYDkmgeSanZHtr3_oUQSmPNdtEeY5pSyckAlffPgF2Fl25Z4zu3iCxeQAW47FrburrC1nvbY-dx5yHvCpzXDYalLbpwrha4DfEQqNv6w6Wu7XGd4xBzn6tjYzO3_hIMpUvhAO3ktvBwuJlD9HA5vr-4iqa3k-uL82mUxkLEUaaIBJ1oynIAYedZOqeKiDnVmnLLUimkEhkDLhUTWgsVM8tV2EouCZeMD9Hp-m_a1N43kJu3xpW26Q0lZtWYgdJ8NxbQ4zX61s1LyH7Bn4oCcLIBrE9tkTe2Sp3_44I2UcnKGa25d1dA_6_QjGc_4g3vfAsfv7xtXo1UXAnzeDMxV4TPnu4ENTH_Alftjz4</recordid><startdate>201210</startdate><enddate>201210</enddate><creator>Ohtani, Shin</creator><creator>Unno, Aiko</creator><creator>Ushiyama, Akira</creator><creator>Kimoto, Takafumi</creator><creator>Miura, Daishiro</creator><creator>Kunugita, Naoki</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201210</creationdate><title>The in vivo Pig-a gene mutation assay is useful for evaluating the genotoxicity of ionizing radiation in mice</title><author>Ohtani, Shin ; Unno, Aiko ; Ushiyama, Akira ; Kimoto, Takafumi ; Miura, Daishiro ; Kunugita, Naoki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4554-d706e98912fee5abdcb1705b19913a2c65675d2e36725995742a3765663603623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Erythrocytes - metabolism</topic><topic>Erythrocytes - radiation effects</topic><topic>Flow Cytometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>genotoxicity</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mutagenicity Tests</topic><topic>Mutation - genetics</topic><topic>Pig-a mutant frequency</topic><topic>Radiation, Ionizing</topic><topic>red blood cells</topic><topic>reticulocytes</topic><topic>Reticulocytes - metabolism</topic><topic>Reticulocytes - radiation effects</topic><topic>Toxicology</topic><topic>X-irradiation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ohtani, Shin</creatorcontrib><creatorcontrib>Unno, Aiko</creatorcontrib><creatorcontrib>Ushiyama, Akira</creatorcontrib><creatorcontrib>Kimoto, Takafumi</creatorcontrib><creatorcontrib>Miura, Daishiro</creatorcontrib><creatorcontrib>Kunugita, Naoki</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Environmental and molecular mutagenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ohtani, Shin</au><au>Unno, Aiko</au><au>Ushiyama, Akira</au><au>Kimoto, Takafumi</au><au>Miura, Daishiro</au><au>Kunugita, Naoki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The in vivo Pig-a gene mutation assay is useful for evaluating the genotoxicity of ionizing radiation in mice</atitle><jtitle>Environmental and molecular mutagenesis</jtitle><addtitle>Environ. Mol. Mutagen</addtitle><date>2012-10</date><risdate>2012</risdate><volume>53</volume><issue>8</issue><spage>579</spage><epage>588</epage><pages>579-588</pages><issn>0893-6692</issn><eissn>1098-2280</eissn><coden>EMMUEG</coden><abstract>The in vivo Pig‐a mutation assay has been adapted for measuring mutation in rats, mice, monkeys, and humans. To date, the assay has been used mainly to assess the mutagenicity of chemicals that are known to be powerful point mutagens. The assay has not been used to measure the biological effects associated with ionizing radiation. In this study, we modified the Pig‐a gene mutation assay (Kimoto et al. [2011b]: Mutat Res 723:36‐42) and used 3‐color staining with fluorescently labeled anti‐CD24, anti‐TER‐119, and anti‐CD71 to detect the Pig‐a mutant frequencies in total red blood cells (RBCs) and in reticulocytes (RETs) from X‐irradiated mice. Single exposures to X‐irradiation resulted in dose‐ and time‐dependent increases in Pig‐a mutant frequencies, and these subsequently declined over time returning to background frequencies. The same total amount of radiation, delivered either as a single dose or as four repeat doses at weekly intervals, increased Pig‐a mutant frequencies to comparable levels, reaching maxima 2–3 weeks after the single dose or 2–3 weeks after the last of the repeat doses. These increased frequencies subsequently returned to background levels. Our results indicated that the 3‐color Pig‐a assay was useful for evaluating the in vivo genotoxicity of radiation. Environ. Mol. Mutagen., 2012. © 2012 Wiley Periodicals, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22911630</pmid><doi>10.1002/em.21724</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cells, Cultured Erythrocytes - metabolism Erythrocytes - radiation effects Flow Cytometry Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution genotoxicity Male Medical sciences Mice Mice, Inbred C57BL Mutagenicity Tests Mutation - genetics Pig-a mutant frequency Radiation, Ionizing red blood cells reticulocytes Reticulocytes - metabolism Reticulocytes - radiation effects Toxicology X-irradiation |
title | The in vivo Pig-a gene mutation assay is useful for evaluating the genotoxicity of ionizing radiation in mice |
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