Paternal Exposure to Bisphenol-A Transgenerationally Impairs Testis Morphology, Germ Cell Associations, and Stemness Properties of Mouse Spermatogonial Stem Cells

Bisphenol-A (BPA) exposure in an adult male can affect the reproductive system, which may also adversely affect the next generation. However, there is a lack of comprehensive data on the BPA-induced disruption of the association and functional characteristics of the testicular germ cells, which the...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of molecular sciences 2020-07, Vol.21 (15), p.5408
Hauptverfasser: Karmakar, Polash Chandra, Ahn, Jin Seop, Kim, Yong-Hee, Jung, Sang-Eun, Kim, Bang-Jin, Lee, Hee-Seok, Kim, Sun-Uk, Rahman, Md Saidur, Pang, Myung-Geol, Ryu, Buom-Yong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 15
container_start_page 5408
container_title International journal of molecular sciences
container_volume 21
creator Karmakar, Polash Chandra
Ahn, Jin Seop
Kim, Yong-Hee
Jung, Sang-Eun
Kim, Bang-Jin
Lee, Hee-Seok
Kim, Sun-Uk
Rahman, Md Saidur
Pang, Myung-Geol
Ryu, Buom-Yong
description Bisphenol-A (BPA) exposure in an adult male can affect the reproductive system, which may also adversely affect the next generation. However, there is a lack of comprehensive data on the BPA-induced disruption of the association and functional characteristics of the testicular germ cells, which the present study sought to investigate. Adult male mice were administered BPA doses by gavage for six consecutive weeks and allowed to breed, producing generations F1-F4. Testis samples from each generation were evaluated for several parameters, including abnormal structure, alterations in germ cell proportions, apoptosis, and loss of functional properties of spermatogonial stem cells (SSCs). We observed that at the lowest-observed-adverse-effect level (LOAEL) dose, the testicular abnormalities and alterations in seminiferous epithelium staging persisted in F0-F2 generations, although a reduced total spermatogonia count was found only in F0. However, abnormalities in the proportions of germ cells were observed until F2. Exposure of the male mice (F0) to BPA alters the morphology of the testis along with the association of germ cells and stemness properties of SSCs, with the effects persisting up to F2. Therefore, we conclude that BPA induces physiological and functional disruption in male germ cells, which may lead to reproductive health issues in the next generation.
doi_str_mv 10.3390/ijms21155408
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7432732</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2430110095</sourcerecordid><originalsourceid>FETCH-LOGICAL-c478t-5110a58d91036f276ef6daa28c9d81b29417432ca6af809a95fea56ebf7027173</originalsourceid><addsrcrecordid>eNpVkU9v1DAQxS0EoqVw44wscd2A_8RxckFaVqVUKqJSl7PlTSa7XiV28DiI_Tp8UrxtqZbTWOPfvHmaR8hbzj5I2bCPbj-i4FypktXPyDkvhSgYq_Tzk_cZeYW4Z0xIoZqX5EwKrbisxTn5c2sTRG8Hevl7CjhHoCnQzw6nHfgwFEu6jtbjFjxEm1zI5HCg1-NkXUS6BkwO6bcQp10YwvawoFcQR7qCYaBLxNC6-yFcUOs7epdg9IBIb2OYICYHSEOfx2cEepc7o01hG7zLdo7svQ6-Ji96OyC8eawX5MeXy_Xqa3Hz_ep6tbwp2lLXqVCcM6vqruFMVr3QFfRVZ62o26ar-UY0JdelFK2tbF-zxjaqB6sq2PSaCc21vCCfHnSneTNC14JP0Q5mim608WCCdeb_H-92Zht-maOsliILvH8UiOHnnE9j9mE-3haNKCXL_lijMrV4oNoYECP0Txs4M8dEzWmiGX936uoJ_heh_Asw9qCO</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2430110095</pqid></control><display><type>article</type><title>Paternal Exposure to Bisphenol-A Transgenerationally Impairs Testis Morphology, Germ Cell Associations, and Stemness Properties of Mouse Spermatogonial Stem Cells</title><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Karmakar, Polash Chandra ; Ahn, Jin Seop ; Kim, Yong-Hee ; Jung, Sang-Eun ; Kim, Bang-Jin ; Lee, Hee-Seok ; Kim, Sun-Uk ; Rahman, Md Saidur ; Pang, Myung-Geol ; Ryu, Buom-Yong</creator><creatorcontrib>Karmakar, Polash Chandra ; Ahn, Jin Seop ; Kim, Yong-Hee ; Jung, Sang-Eun ; Kim, Bang-Jin ; Lee, Hee-Seok ; Kim, Sun-Uk ; Rahman, Md Saidur ; Pang, Myung-Geol ; Ryu, Buom-Yong</creatorcontrib><description>Bisphenol-A (BPA) exposure in an adult male can affect the reproductive system, which may also adversely affect the next generation. However, there is a lack of comprehensive data on the BPA-induced disruption of the association and functional characteristics of the testicular germ cells, which the present study sought to investigate. Adult male mice were administered BPA doses by gavage for six consecutive weeks and allowed to breed, producing generations F1-F4. Testis samples from each generation were evaluated for several parameters, including abnormal structure, alterations in germ cell proportions, apoptosis, and loss of functional properties of spermatogonial stem cells (SSCs). We observed that at the lowest-observed-adverse-effect level (LOAEL) dose, the testicular abnormalities and alterations in seminiferous epithelium staging persisted in F0-F2 generations, although a reduced total spermatogonia count was found only in F0. However, abnormalities in the proportions of germ cells were observed until F2. Exposure of the male mice (F0) to BPA alters the morphology of the testis along with the association of germ cells and stemness properties of SSCs, with the effects persisting up to F2. Therefore, we conclude that BPA induces physiological and functional disruption in male germ cells, which may lead to reproductive health issues in the next generation.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms21155408</identifier><identifier>PMID: 32751382</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Abnormalities ; Animals ; Apoptosis ; Apoptosis - drug effects ; Benzhydryl Compounds - toxicity ; Bisphenol A ; Cell Count ; Cytology ; Deoxyribonucleic acid ; Disruption ; DNA ; DNA damage ; DNA methylation ; Endocrine Disruptors - toxicity ; Epithelium ; Exposure ; Female ; Germ cells ; Humans ; Male ; Mice ; Mice, Inbred ICR ; Morphology ; Paternal Exposure ; Phenols - toxicity ; Physiological effects ; Pregnancy ; Prenatal Exposure Delayed Effects - chemically induced ; Prenatal Exposure Delayed Effects - metabolism ; Prenatal Exposure Delayed Effects - pathology ; Reproductive system ; Sperm ; Spermatogenesis ; Spermatogonia ; Spermatogonia - drug effects ; Spermatogonia - metabolism ; Spermatogonia - pathology ; Stem cell transplantation ; Stem cells ; Stem Cells - drug effects ; Stem Cells - metabolism ; Stem Cells - pathology ; Testes ; Testis - drug effects ; Testis - metabolism ; Testis - pathology</subject><ispartof>International journal of molecular sciences, 2020-07, Vol.21 (15), p.5408</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-5110a58d91036f276ef6daa28c9d81b29417432ca6af809a95fea56ebf7027173</citedby><cites>FETCH-LOGICAL-c478t-5110a58d91036f276ef6daa28c9d81b29417432ca6af809a95fea56ebf7027173</cites><orcidid>0000-0001-9244-0561 ; 0000-0003-2019-3789 ; 0000-0003-4583-8731</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432732/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432732/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32751382$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karmakar, Polash Chandra</creatorcontrib><creatorcontrib>Ahn, Jin Seop</creatorcontrib><creatorcontrib>Kim, Yong-Hee</creatorcontrib><creatorcontrib>Jung, Sang-Eun</creatorcontrib><creatorcontrib>Kim, Bang-Jin</creatorcontrib><creatorcontrib>Lee, Hee-Seok</creatorcontrib><creatorcontrib>Kim, Sun-Uk</creatorcontrib><creatorcontrib>Rahman, Md Saidur</creatorcontrib><creatorcontrib>Pang, Myung-Geol</creatorcontrib><creatorcontrib>Ryu, Buom-Yong</creatorcontrib><title>Paternal Exposure to Bisphenol-A Transgenerationally Impairs Testis Morphology, Germ Cell Associations, and Stemness Properties of Mouse Spermatogonial Stem Cells</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Bisphenol-A (BPA) exposure in an adult male can affect the reproductive system, which may also adversely affect the next generation. However, there is a lack of comprehensive data on the BPA-induced disruption of the association and functional characteristics of the testicular germ cells, which the present study sought to investigate. Adult male mice were administered BPA doses by gavage for six consecutive weeks and allowed to breed, producing generations F1-F4. Testis samples from each generation were evaluated for several parameters, including abnormal structure, alterations in germ cell proportions, apoptosis, and loss of functional properties of spermatogonial stem cells (SSCs). We observed that at the lowest-observed-adverse-effect level (LOAEL) dose, the testicular abnormalities and alterations in seminiferous epithelium staging persisted in F0-F2 generations, although a reduced total spermatogonia count was found only in F0. However, abnormalities in the proportions of germ cells were observed until F2. Exposure of the male mice (F0) to BPA alters the morphology of the testis along with the association of germ cells and stemness properties of SSCs, with the effects persisting up to F2. Therefore, we conclude that BPA induces physiological and functional disruption in male germ cells, which may lead to reproductive health issues in the next generation.</description><subject>Abnormalities</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Benzhydryl Compounds - toxicity</subject><subject>Bisphenol A</subject><subject>Cell Count</subject><subject>Cytology</subject><subject>Deoxyribonucleic acid</subject><subject>Disruption</subject><subject>DNA</subject><subject>DNA damage</subject><subject>DNA methylation</subject><subject>Endocrine Disruptors - toxicity</subject><subject>Epithelium</subject><subject>Exposure</subject><subject>Female</subject><subject>Germ cells</subject><subject>Humans</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Morphology</subject><subject>Paternal Exposure</subject><subject>Phenols - toxicity</subject><subject>Physiological effects</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects - chemically induced</subject><subject>Prenatal Exposure Delayed Effects - metabolism</subject><subject>Prenatal Exposure Delayed Effects - pathology</subject><subject>Reproductive system</subject><subject>Sperm</subject><subject>Spermatogenesis</subject><subject>Spermatogonia</subject><subject>Spermatogonia - drug effects</subject><subject>Spermatogonia - metabolism</subject><subject>Spermatogonia - pathology</subject><subject>Stem cell transplantation</subject><subject>Stem cells</subject><subject>Stem Cells - drug effects</subject><subject>Stem Cells - metabolism</subject><subject>Stem Cells - pathology</subject><subject>Testes</subject><subject>Testis - drug effects</subject><subject>Testis - metabolism</subject><subject>Testis - pathology</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpVkU9v1DAQxS0EoqVw44wscd2A_8RxckFaVqVUKqJSl7PlTSa7XiV28DiI_Tp8UrxtqZbTWOPfvHmaR8hbzj5I2bCPbj-i4FypktXPyDkvhSgYq_Tzk_cZeYW4Z0xIoZqX5EwKrbisxTn5c2sTRG8Hevl7CjhHoCnQzw6nHfgwFEu6jtbjFjxEm1zI5HCg1-NkXUS6BkwO6bcQp10YwvawoFcQR7qCYaBLxNC6-yFcUOs7epdg9IBIb2OYICYHSEOfx2cEepc7o01hG7zLdo7svQ6-Ji96OyC8eawX5MeXy_Xqa3Hz_ep6tbwp2lLXqVCcM6vqruFMVr3QFfRVZ62o26ar-UY0JdelFK2tbF-zxjaqB6sq2PSaCc21vCCfHnSneTNC14JP0Q5mim608WCCdeb_H-92Zht-maOsliILvH8UiOHnnE9j9mE-3haNKCXL_lijMrV4oNoYECP0Txs4M8dEzWmiGX936uoJ_heh_Asw9qCO</recordid><startdate>20200729</startdate><enddate>20200729</enddate><creator>Karmakar, Polash Chandra</creator><creator>Ahn, Jin Seop</creator><creator>Kim, Yong-Hee</creator><creator>Jung, Sang-Eun</creator><creator>Kim, Bang-Jin</creator><creator>Lee, Hee-Seok</creator><creator>Kim, Sun-Uk</creator><creator>Rahman, Md Saidur</creator><creator>Pang, Myung-Geol</creator><creator>Ryu, Buom-Yong</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9244-0561</orcidid><orcidid>https://orcid.org/0000-0003-2019-3789</orcidid><orcidid>https://orcid.org/0000-0003-4583-8731</orcidid></search><sort><creationdate>20200729</creationdate><title>Paternal Exposure to Bisphenol-A Transgenerationally Impairs Testis Morphology, Germ Cell Associations, and Stemness Properties of Mouse Spermatogonial Stem Cells</title><author>Karmakar, Polash Chandra ; Ahn, Jin Seop ; Kim, Yong-Hee ; Jung, Sang-Eun ; Kim, Bang-Jin ; Lee, Hee-Seok ; Kim, Sun-Uk ; Rahman, Md Saidur ; Pang, Myung-Geol ; Ryu, Buom-Yong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-5110a58d91036f276ef6daa28c9d81b29417432ca6af809a95fea56ebf7027173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Abnormalities</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Benzhydryl Compounds - toxicity</topic><topic>Bisphenol A</topic><topic>Cell Count</topic><topic>Cytology</topic><topic>Deoxyribonucleic acid</topic><topic>Disruption</topic><topic>DNA</topic><topic>DNA damage</topic><topic>DNA methylation</topic><topic>Endocrine Disruptors - toxicity</topic><topic>Epithelium</topic><topic>Exposure</topic><topic>Female</topic><topic>Germ cells</topic><topic>Humans</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Morphology</topic><topic>Paternal Exposure</topic><topic>Phenols - toxicity</topic><topic>Physiological effects</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects - chemically induced</topic><topic>Prenatal Exposure Delayed Effects - metabolism</topic><topic>Prenatal Exposure Delayed Effects - pathology</topic><topic>Reproductive system</topic><topic>Sperm</topic><topic>Spermatogenesis</topic><topic>Spermatogonia</topic><topic>Spermatogonia - drug effects</topic><topic>Spermatogonia - metabolism</topic><topic>Spermatogonia - pathology</topic><topic>Stem cell transplantation</topic><topic>Stem cells</topic><topic>Stem Cells - drug effects</topic><topic>Stem Cells - metabolism</topic><topic>Stem Cells - pathology</topic><topic>Testes</topic><topic>Testis - drug effects</topic><topic>Testis - metabolism</topic><topic>Testis - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karmakar, Polash Chandra</creatorcontrib><creatorcontrib>Ahn, Jin Seop</creatorcontrib><creatorcontrib>Kim, Yong-Hee</creatorcontrib><creatorcontrib>Jung, Sang-Eun</creatorcontrib><creatorcontrib>Kim, Bang-Jin</creatorcontrib><creatorcontrib>Lee, Hee-Seok</creatorcontrib><creatorcontrib>Kim, Sun-Uk</creatorcontrib><creatorcontrib>Rahman, Md Saidur</creatorcontrib><creatorcontrib>Pang, Myung-Geol</creatorcontrib><creatorcontrib>Ryu, Buom-Yong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karmakar, Polash Chandra</au><au>Ahn, Jin Seop</au><au>Kim, Yong-Hee</au><au>Jung, Sang-Eun</au><au>Kim, Bang-Jin</au><au>Lee, Hee-Seok</au><au>Kim, Sun-Uk</au><au>Rahman, Md Saidur</au><au>Pang, Myung-Geol</au><au>Ryu, Buom-Yong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Paternal Exposure to Bisphenol-A Transgenerationally Impairs Testis Morphology, Germ Cell Associations, and Stemness Properties of Mouse Spermatogonial Stem Cells</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2020-07-29</date><risdate>2020</risdate><volume>21</volume><issue>15</issue><spage>5408</spage><pages>5408-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Bisphenol-A (BPA) exposure in an adult male can affect the reproductive system, which may also adversely affect the next generation. However, there is a lack of comprehensive data on the BPA-induced disruption of the association and functional characteristics of the testicular germ cells, which the present study sought to investigate. Adult male mice were administered BPA doses by gavage for six consecutive weeks and allowed to breed, producing generations F1-F4. Testis samples from each generation were evaluated for several parameters, including abnormal structure, alterations in germ cell proportions, apoptosis, and loss of functional properties of spermatogonial stem cells (SSCs). We observed that at the lowest-observed-adverse-effect level (LOAEL) dose, the testicular abnormalities and alterations in seminiferous epithelium staging persisted in F0-F2 generations, although a reduced total spermatogonia count was found only in F0. However, abnormalities in the proportions of germ cells were observed until F2. Exposure of the male mice (F0) to BPA alters the morphology of the testis along with the association of germ cells and stemness properties of SSCs, with the effects persisting up to F2. Therefore, we conclude that BPA induces physiological and functional disruption in male germ cells, which may lead to reproductive health issues in the next generation.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>32751382</pmid><doi>10.3390/ijms21155408</doi><orcidid>https://orcid.org/0000-0001-9244-0561</orcidid><orcidid>https://orcid.org/0000-0003-2019-3789</orcidid><orcidid>https://orcid.org/0000-0003-4583-8731</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1422-0067
ispartof International journal of molecular sciences, 2020-07, Vol.21 (15), p.5408
issn 1422-0067
1661-6596
1422-0067
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7432732
source MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Abnormalities
Animals
Apoptosis
Apoptosis - drug effects
Benzhydryl Compounds - toxicity
Bisphenol A
Cell Count
Cytology
Deoxyribonucleic acid
Disruption
DNA
DNA damage
DNA methylation
Endocrine Disruptors - toxicity
Epithelium
Exposure
Female
Germ cells
Humans
Male
Mice
Mice, Inbred ICR
Morphology
Paternal Exposure
Phenols - toxicity
Physiological effects
Pregnancy
Prenatal Exposure Delayed Effects - chemically induced
Prenatal Exposure Delayed Effects - metabolism
Prenatal Exposure Delayed Effects - pathology
Reproductive system
Sperm
Spermatogenesis
Spermatogonia
Spermatogonia - drug effects
Spermatogonia - metabolism
Spermatogonia - pathology
Stem cell transplantation
Stem cells
Stem Cells - drug effects
Stem Cells - metabolism
Stem Cells - pathology
Testes
Testis - drug effects
Testis - metabolism
Testis - pathology
title Paternal Exposure to Bisphenol-A Transgenerationally Impairs Testis Morphology, Germ Cell Associations, and Stemness Properties of Mouse Spermatogonial Stem Cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T22%3A17%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Paternal%20Exposure%20to%20Bisphenol-A%20Transgenerationally%20Impairs%20Testis%20Morphology,%20Germ%20Cell%20Associations,%20and%20Stemness%20Properties%20of%20Mouse%20Spermatogonial%20Stem%20Cells&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Karmakar,%20Polash%20Chandra&rft.date=2020-07-29&rft.volume=21&rft.issue=15&rft.spage=5408&rft.pages=5408-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms21155408&rft_dat=%3Cproquest_pubme%3E2430110095%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2430110095&rft_id=info:pmid/32751382&rfr_iscdi=true