Sex-specific differences in fetal germ cell apoptosis induced by ionizing radiation
BACKGROUND We have previously shown that male human fetal germ cells are highly radiosensitive and that their death depends on p53 activation. Male germ cell apoptosis was initiated with doses as low as 0.1 Gy and was prevented by pifithrin α, a p53 inhibitor. In this study, we investigated the radi...
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Veröffentlicht in: | Human reproduction (Oxford) 2009-03, Vol.24 (3), p.670-678 |
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creator | Guerquin, Marie-Justine Duquenne, Clotilde Coffigny, Hervé Rouiller-Fabre, Virginie Lambrot, Romain Bakalska, Mariana Frydman, René Habert, René Livera, Gabriel |
description | BACKGROUND We have previously shown that male human fetal germ cells are highly radiosensitive and that their death depends on p53 activation. Male germ cell apoptosis was initiated with doses as low as 0.1 Gy and was prevented by pifithrin α, a p53 inhibitor. In this study, we investigated the radiosensitivity of early female and male fetal proliferating germ cells. METHODS AND RESULTS Both male and female fetal germ cells displayed a similar number of γH2AX foci in response to ionizing radiation (IR). In organ culture of human fetal ovaries, the germ cells underwent apoptosis only when exposed to high doses of IR (1.5 Gy and above). Accumulation of p53 was detected in irradiated male human fetal germ cells but not in female ones. Inhibition of p53 with pifithrin α did not affect oogonia apoptosis following irradiation. IR induced apoptosis similarly in mouse fetal ovaries in organ culture and in vivo during oogonial proliferation. Germ cell survival in testes from p53 knockout or p63 knockout mice exposed to IR was better than wild-type, whereas female germ cell survival was unaffected by p53 or p63 knockout. CONCLUSIONS These findings show that pre-meiotic male and female fetal germ cells behave differently in response to a genotoxic stress—irradiation—with oogonia being less sensitive and undergoing p53-independent apoptosis. |
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Male germ cell apoptosis was initiated with doses as low as 0.1 Gy and was prevented by pifithrin α, a p53 inhibitor. In this study, we investigated the radiosensitivity of early female and male fetal proliferating germ cells. METHODS AND RESULTS Both male and female fetal germ cells displayed a similar number of γH2AX foci in response to ionizing radiation (IR). In organ culture of human fetal ovaries, the germ cells underwent apoptosis only when exposed to high doses of IR (1.5 Gy and above). Accumulation of p53 was detected in irradiated male human fetal germ cells but not in female ones. Inhibition of p53 with pifithrin α did not affect oogonia apoptosis following irradiation. IR induced apoptosis similarly in mouse fetal ovaries in organ culture and in vivo during oogonial proliferation. Germ cell survival in testes from p53 knockout or p63 knockout mice exposed to IR was better than wild-type, whereas female germ cell survival was unaffected by p53 or p63 knockout. CONCLUSIONS These findings show that pre-meiotic male and female fetal germ cells behave differently in response to a genotoxic stress—irradiation—with oogonia being less sensitive and undergoing p53-independent apoptosis.</description><identifier>ISSN: 0268-1161</identifier><identifier>EISSN: 1460-2350</identifier><identifier>DOI: 10.1093/humrep/den410</identifier><identifier>PMID: 19088112</identifier><identifier>CODEN: HUREEE</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Animals ; Apoptosis ; Benzothiazoles - pharmacology ; Biological and medical sciences ; Dose-Response Relationship, Radiation ; Female ; Genes, p53 ; Germ Cells - cytology ; Germ Cells - radiation effects ; gonocyte ; Gynecology. Andrology. Obstetrics ; Histones - metabolism ; Humans ; ionizing radiation ; Male ; Medical sciences ; Mice ; Mice, Transgenic ; oogonia ; Organ Culture Techniques - methods ; p53 ; Radiation, Ionizing ; Sex Factors ; Toluene - analogs & derivatives ; Toluene - pharmacology</subject><ispartof>Human reproduction (Oxford), 2009-03, Vol.24 (3), p.670-678</ispartof><rights>The Author 2008. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2009</rights><rights>2009 INIST-CNRS</rights><rights>The Author 2008. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-64f4ca854fec80e6e17efe840ec4daaf331294926999294a148e0b0ef6cd8e213</citedby><cites>FETCH-LOGICAL-c458t-64f4ca854fec80e6e17efe840ec4daaf331294926999294a148e0b0ef6cd8e213</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21148334$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19088112$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guerquin, Marie-Justine</creatorcontrib><creatorcontrib>Duquenne, Clotilde</creatorcontrib><creatorcontrib>Coffigny, Hervé</creatorcontrib><creatorcontrib>Rouiller-Fabre, Virginie</creatorcontrib><creatorcontrib>Lambrot, Romain</creatorcontrib><creatorcontrib>Bakalska, Mariana</creatorcontrib><creatorcontrib>Frydman, René</creatorcontrib><creatorcontrib>Habert, René</creatorcontrib><creatorcontrib>Livera, Gabriel</creatorcontrib><title>Sex-specific differences in fetal germ cell apoptosis induced by ionizing radiation</title><title>Human reproduction (Oxford)</title><addtitle>Hum Reprod</addtitle><description>BACKGROUND We have previously shown that male human fetal germ cells are highly radiosensitive and that their death depends on p53 activation. Male germ cell apoptosis was initiated with doses as low as 0.1 Gy and was prevented by pifithrin α, a p53 inhibitor. In this study, we investigated the radiosensitivity of early female and male fetal proliferating germ cells. METHODS AND RESULTS Both male and female fetal germ cells displayed a similar number of γH2AX foci in response to ionizing radiation (IR). In organ culture of human fetal ovaries, the germ cells underwent apoptosis only when exposed to high doses of IR (1.5 Gy and above). Accumulation of p53 was detected in irradiated male human fetal germ cells but not in female ones. Inhibition of p53 with pifithrin α did not affect oogonia apoptosis following irradiation. IR induced apoptosis similarly in mouse fetal ovaries in organ culture and in vivo during oogonial proliferation. Germ cell survival in testes from p53 knockout or p63 knockout mice exposed to IR was better than wild-type, whereas female germ cell survival was unaffected by p53 or p63 knockout. CONCLUSIONS These findings show that pre-meiotic male and female fetal germ cells behave differently in response to a genotoxic stress—irradiation—with oogonia being less sensitive and undergoing p53-independent apoptosis.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Benzothiazoles - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Dose-Response Relationship, Radiation</subject><subject>Female</subject><subject>Genes, p53</subject><subject>Germ Cells - cytology</subject><subject>Germ Cells - radiation effects</subject><subject>gonocyte</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Histones - metabolism</subject><subject>Humans</subject><subject>ionizing radiation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>oogonia</subject><subject>Organ Culture Techniques - methods</subject><subject>p53</subject><subject>Radiation, Ionizing</subject><subject>Sex Factors</subject><subject>Toluene - analogs & derivatives</subject><subject>Toluene - pharmacology</subject><issn>0268-1161</issn><issn>1460-2350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0MFLHDEUBvBQlLraHnstQSh4Gc1LstnMsSxdV1A82Jall5DNvNjY2ZkxmYHVv97IDPboKS_kx_vCR8gXYOfASnHxd9hF7C4qbCSwD2QGUrGCizk7IDPGlS4AFByR45QeGMujVh_JEZRMawA-I3d3uC9Shy744GgVvMeIjcNEQ0M99ram9xh31GFdU9u1Xd-m8PpYDQ4run2ioW3Cc2juabRVsH2-fiKH3tYJP0_nCfm1-vFzuS6uby-vlt-vCyfnui-U9NJZPZcenWaoEBboUUuGTlbWeiGAl7LkqizLPFiQGtmWoVeu0shBnJDTcW8X28cBU28e2iE2OdJwAC0WwHhGxYhcbFOK6E0Xw87GJwPMvDZoxgbN2GD2X6elw3aH1X89VZbBtwnY5Gzto21cSG8uJ0sthMzubHTt0L2bOf0xpB73b9jGf0YtxGJu1ps_pmQ3q9-wuTRcvACThphj</recordid><startdate>20090301</startdate><enddate>20090301</enddate><creator>Guerquin, Marie-Justine</creator><creator>Duquenne, Clotilde</creator><creator>Coffigny, Hervé</creator><creator>Rouiller-Fabre, Virginie</creator><creator>Lambrot, Romain</creator><creator>Bakalska, Mariana</creator><creator>Frydman, René</creator><creator>Habert, René</creator><creator>Livera, Gabriel</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</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><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20090301</creationdate><title>Sex-specific differences in fetal germ cell apoptosis induced by ionizing radiation</title><author>Guerquin, Marie-Justine ; Duquenne, Clotilde ; Coffigny, Hervé ; Rouiller-Fabre, Virginie ; Lambrot, Romain ; Bakalska, Mariana ; Frydman, René ; Habert, René ; Livera, Gabriel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-64f4ca854fec80e6e17efe840ec4daaf331294926999294a148e0b0ef6cd8e213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Benzothiazoles - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Dose-Response Relationship, Radiation</topic><topic>Female</topic><topic>Genes, p53</topic><topic>Germ Cells - cytology</topic><topic>Germ Cells - radiation effects</topic><topic>gonocyte</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Histones - metabolism</topic><topic>Humans</topic><topic>ionizing radiation</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>oogonia</topic><topic>Organ Culture Techniques - methods</topic><topic>p53</topic><topic>Radiation, Ionizing</topic><topic>Sex Factors</topic><topic>Toluene - analogs & derivatives</topic><topic>Toluene - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guerquin, Marie-Justine</creatorcontrib><creatorcontrib>Duquenne, Clotilde</creatorcontrib><creatorcontrib>Coffigny, Hervé</creatorcontrib><creatorcontrib>Rouiller-Fabre, Virginie</creatorcontrib><creatorcontrib>Lambrot, Romain</creatorcontrib><creatorcontrib>Bakalska, Mariana</creatorcontrib><creatorcontrib>Frydman, René</creatorcontrib><creatorcontrib>Habert, René</creatorcontrib><creatorcontrib>Livera, Gabriel</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><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guerquin, Marie-Justine</au><au>Duquenne, Clotilde</au><au>Coffigny, Hervé</au><au>Rouiller-Fabre, Virginie</au><au>Lambrot, Romain</au><au>Bakalska, Mariana</au><au>Frydman, René</au><au>Habert, René</au><au>Livera, Gabriel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sex-specific differences in fetal germ cell apoptosis induced by ionizing radiation</atitle><jtitle>Human reproduction (Oxford)</jtitle><addtitle>Hum Reprod</addtitle><date>2009-03-01</date><risdate>2009</risdate><volume>24</volume><issue>3</issue><spage>670</spage><epage>678</epage><pages>670-678</pages><issn>0268-1161</issn><eissn>1460-2350</eissn><coden>HUREEE</coden><abstract>BACKGROUND We have previously shown that male human fetal germ cells are highly radiosensitive and that their death depends on p53 activation. Male germ cell apoptosis was initiated with doses as low as 0.1 Gy and was prevented by pifithrin α, a p53 inhibitor. In this study, we investigated the radiosensitivity of early female and male fetal proliferating germ cells. METHODS AND RESULTS Both male and female fetal germ cells displayed a similar number of γH2AX foci in response to ionizing radiation (IR). In organ culture of human fetal ovaries, the germ cells underwent apoptosis only when exposed to high doses of IR (1.5 Gy and above). Accumulation of p53 was detected in irradiated male human fetal germ cells but not in female ones. Inhibition of p53 with pifithrin α did not affect oogonia apoptosis following irradiation. IR induced apoptosis similarly in mouse fetal ovaries in organ culture and in vivo during oogonial proliferation. Germ cell survival in testes from p53 knockout or p63 knockout mice exposed to IR was better than wild-type, whereas female germ cell survival was unaffected by p53 or p63 knockout. CONCLUSIONS These findings show that pre-meiotic male and female fetal germ cells behave differently in response to a genotoxic stress—irradiation—with oogonia being less sensitive and undergoing p53-independent apoptosis.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>19088112</pmid><doi>10.1093/humrep/den410</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis Benzothiazoles - pharmacology Biological and medical sciences Dose-Response Relationship, Radiation Female Genes, p53 Germ Cells - cytology Germ Cells - radiation effects gonocyte Gynecology. Andrology. Obstetrics Histones - metabolism Humans ionizing radiation Male Medical sciences Mice Mice, Transgenic oogonia Organ Culture Techniques - methods p53 Radiation, Ionizing Sex Factors Toluene - analogs & derivatives Toluene - pharmacology |
title | Sex-specific differences in fetal germ cell apoptosis induced by ionizing radiation |
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