The response of human mesenchymal stem cells to internal exposure to tritium β-rays
There is no doubt that estimating the exposure risk of external and internal low-dose radiation is an imperative issue in radiobiological study. Human mesenchymal stem cells (hMSCs) are multipotent and self-renewing, supporting the regeneration of damaged tissue, including tissue damaged by radiatio...
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Veröffentlicht in: | Journal of radiation research 2019-07, Vol.60 (4), p.476-482 |
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description | There is no doubt that estimating the exposure risk of external and internal low-dose radiation is an imperative issue in radiobiological study. Human mesenchymal stem cells (hMSCs) are multipotent and self-renewing, supporting the regeneration of damaged tissue, including tissue damaged by radiation. However, the responses of hMSCs to internal exposure to radionuclides are still insufficiently understood. In order to evaluate the adverse effects produced by internal exposure to tritiated water (HTO) at a low dose, hMSCs were exposed to 2 × 107 Bq/ml HTO, and the biological effects after the exposure were examined. Apoptosis and DNA double-strand breaks (DSBs) were assayed to analyze the cellular response to the damage induced by HTO. Slight enhancement of apoptosis was found after treatment, except at the dose of 9 mGy. The number of DSBs at 24 h post-irradiation showed that the DNA damage was able to be efficiently repaired by the hMSCs. Moreover, the increasing proportion of the cell population in S phase proved that the persistence of residual γH2AX foci at lower concentrations of HTO was attributable to the secondary production of DSBs in DNA replication. Our work adds to the available data, helping us understand the risk of stem cell transformation due to internal exposure and its correlation with low-dose radiation-induced carcinogenesis. |
doi_str_mv | 10.1093/jrr/rrz037 |
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Human mesenchymal stem cells (hMSCs) are multipotent and self-renewing, supporting the regeneration of damaged tissue, including tissue damaged by radiation. However, the responses of hMSCs to internal exposure to radionuclides are still insufficiently understood. In order to evaluate the adverse effects produced by internal exposure to tritiated water (HTO) at a low dose, hMSCs were exposed to 2 × 107 Bq/ml HTO, and the biological effects after the exposure were examined. Apoptosis and DNA double-strand breaks (DSBs) were assayed to analyze the cellular response to the damage induced by HTO. Slight enhancement of apoptosis was found after treatment, except at the dose of 9 mGy. The number of DSBs at 24 h post-irradiation showed that the DNA damage was able to be efficiently repaired by the hMSCs. Moreover, the increasing proportion of the cell population in S phase proved that the persistence of residual γH2AX foci at lower concentrations of HTO was attributable to the secondary production of DSBs in DNA replication. Our work adds to the available data, helping us understand the risk of stem cell transformation due to internal exposure and its correlation with low-dose radiation-induced carcinogenesis.</description><identifier>ISSN: 0449-3060</identifier><identifier>EISSN: 1349-9157</identifier><identifier>DOI: 10.1093/jrr/rrz037</identifier><identifier>PMID: 31165153</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Apoptosis - radiation effects ; Beta Particles ; Cell Cycle - radiation effects ; Cells, Cultured ; DNA Breaks, Double-Stranded - radiation effects ; DNA Replication - radiation effects ; Histones - metabolism ; Humans ; Mesenchymal Stem Cells - radiation effects ; Radioisotopes ; Short Communication ; Tritium - chemistry ; Water</subject><ispartof>Journal of radiation research, 2019-07, Vol.60 (4), p.476-482</ispartof><rights>The Author(s) 2019. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology.</rights><rights>The Author(s) 2019. 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Human mesenchymal stem cells (hMSCs) are multipotent and self-renewing, supporting the regeneration of damaged tissue, including tissue damaged by radiation. However, the responses of hMSCs to internal exposure to radionuclides are still insufficiently understood. In order to evaluate the adverse effects produced by internal exposure to tritiated water (HTO) at a low dose, hMSCs were exposed to 2 × 107 Bq/ml HTO, and the biological effects after the exposure were examined. Apoptosis and DNA double-strand breaks (DSBs) were assayed to analyze the cellular response to the damage induced by HTO. Slight enhancement of apoptosis was found after treatment, except at the dose of 9 mGy. The number of DSBs at 24 h post-irradiation showed that the DNA damage was able to be efficiently repaired by the hMSCs. Moreover, the increasing proportion of the cell population in S phase proved that the persistence of residual γH2AX foci at lower concentrations of HTO was attributable to the secondary production of DSBs in DNA replication. Our work adds to the available data, helping us understand the risk of stem cell transformation due to internal exposure and its correlation with low-dose radiation-induced carcinogenesis.</description><subject>Apoptosis - radiation effects</subject><subject>Beta Particles</subject><subject>Cell Cycle - radiation effects</subject><subject>Cells, Cultured</subject><subject>DNA Breaks, Double-Stranded - radiation effects</subject><subject>DNA Replication - radiation effects</subject><subject>Histones - metabolism</subject><subject>Humans</subject><subject>Mesenchymal Stem Cells - radiation effects</subject><subject>Radioisotopes</subject><subject>Short Communication</subject><subject>Tritium - chemistry</subject><subject>Water</subject><issn>0449-3060</issn><issn>1349-9157</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkNtKw0AQhhdRbK3e-ACy10Ls7CnJ3gginqDgTb1eNpuJScmJ3VSsj-WD-EymVItezfDPP_8MHyHnDK4YaDFfeT_3_gNEckCmTEgdaaaSQzIFOfYCYpiQkxBWADwBBcdkIhiLFVNiSpbLEqnH0HdtQNoVtFw3tqUNBmxduWlsTcOADXVY14EOHa3aAX07yvjed2HtcSsOvhqqdUO_PiNvN-GUHBW2Dnj2U2fk5f5uefsYLZ4fnm5vFpGTwIfIqjyHIi0UH_9hWQFW5lIWoHOZaeTKpYlW3MUchUryFDVPEhtbrqzDlGW5mJHrXW6_zhrMHbaDt7XpfdVYvzGdrcz_SVuV5rV7M3EsQTMYAy53Ac53IXgs9rsMzJatGdmaHdvRfPH32t76C1N8AzALea8</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Quan, Yi</creator><creator>Lin, Jinxian</creator><creator>Deng, Bing</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1759-8518</orcidid></search><sort><creationdate>20190701</creationdate><title>The response of human mesenchymal stem cells to internal exposure to tritium β-rays</title><author>Quan, Yi ; Lin, Jinxian ; Deng, Bing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-a5dd0f8f523111bf0a4d44f09d4b9e25c87952c62e357d8e9277a6a25ace81bd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Apoptosis - radiation effects</topic><topic>Beta Particles</topic><topic>Cell Cycle - radiation effects</topic><topic>Cells, Cultured</topic><topic>DNA Breaks, Double-Stranded - radiation effects</topic><topic>DNA Replication - radiation effects</topic><topic>Histones - metabolism</topic><topic>Humans</topic><topic>Mesenchymal Stem Cells - radiation effects</topic><topic>Radioisotopes</topic><topic>Short Communication</topic><topic>Tritium - chemistry</topic><topic>Water</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quan, Yi</creatorcontrib><creatorcontrib>Lin, Jinxian</creatorcontrib><creatorcontrib>Deng, Bing</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of radiation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quan, Yi</au><au>Lin, Jinxian</au><au>Deng, Bing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The response of human mesenchymal stem cells to internal exposure to tritium β-rays</atitle><jtitle>Journal of radiation research</jtitle><addtitle>J Radiat Res</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>60</volume><issue>4</issue><spage>476</spage><epage>482</epage><pages>476-482</pages><issn>0449-3060</issn><eissn>1349-9157</eissn><abstract>There is no doubt that estimating the exposure risk of external and internal low-dose radiation is an imperative issue in radiobiological study. Human mesenchymal stem cells (hMSCs) are multipotent and self-renewing, supporting the regeneration of damaged tissue, including tissue damaged by radiation. However, the responses of hMSCs to internal exposure to radionuclides are still insufficiently understood. In order to evaluate the adverse effects produced by internal exposure to tritiated water (HTO) at a low dose, hMSCs were exposed to 2 × 107 Bq/ml HTO, and the biological effects after the exposure were examined. Apoptosis and DNA double-strand breaks (DSBs) were assayed to analyze the cellular response to the damage induced by HTO. Slight enhancement of apoptosis was found after treatment, except at the dose of 9 mGy. The number of DSBs at 24 h post-irradiation showed that the DNA damage was able to be efficiently repaired by the hMSCs. Moreover, the increasing proportion of the cell population in S phase proved that the persistence of residual γH2AX foci at lower concentrations of HTO was attributable to the secondary production of DSBs in DNA replication. Our work adds to the available data, helping us understand the risk of stem cell transformation due to internal exposure and its correlation with low-dose radiation-induced carcinogenesis.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>31165153</pmid><doi>10.1093/jrr/rrz037</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-1759-8518</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis - radiation effects Beta Particles Cell Cycle - radiation effects Cells, Cultured DNA Breaks, Double-Stranded - radiation effects DNA Replication - radiation effects Histones - metabolism Humans Mesenchymal Stem Cells - radiation effects Radioisotopes Short Communication Tritium - chemistry Water |
title | The response of human mesenchymal stem cells to internal exposure to tritium β-rays |
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