Loading…

High-content imaging analyses of the effects of bisphenols and organophosphate esters on TM4 mouse Sertoli cells

The endocrine disruptive effects of bisphenol A (BPA) and brominated flame retardants (BDE-47) have led to restrictions on their use and increased the pressure to identify safe replacements for these chemicals. Although there is evidence that some of these alternatives may be toxic to spermatogonial...

Full description

Saved in:
Bibliographic Details
Published in:Biology of reproduction 2022-09, Vol.107 (3), p.858-868
Main Authors: Rajkumar, Abishankari, Luu, Trang, Hales, Barbara F., Robaire, Bernard
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-b489t-931012ad0f319ed9adcbd55e9f40b4cc4d9780ee243b2695ab5d0d4044fb702a3
cites cdi_FETCH-LOGICAL-b489t-931012ad0f319ed9adcbd55e9f40b4cc4d9780ee243b2695ab5d0d4044fb702a3
container_end_page 868
container_issue 3
container_start_page 858
container_title Biology of reproduction
container_volume 107
creator Rajkumar, Abishankari
Luu, Trang
Hales, Barbara F.
Robaire, Bernard
description The endocrine disruptive effects of bisphenol A (BPA) and brominated flame retardants (BDE-47) have led to restrictions on their use and increased the pressure to identify safe replacements for these chemicals. Although there is evidence that some of these alternatives may be toxic to spermatogonial and Leydig cells, little is known about the toxicity of emerging replacements on Sertoli cells. We used high-content imaging to compare the effects of legacy chemicals, BPA and BDE-47, to their corresponding replacements. TM4 Sertoli cells were exposed for 48 h to each chemical (0.001–100 µM) followed by cytotoxicity and phenotypic endpoint assessment. The benchmark concentration potency ranking for bisphenols based on cytotoxicity was BPTMC > bisphenol M > BPAF>BPF > BPS > BPA. Human administered equivalent dose (AED) determination ranked BPS as the most potent alternative replacement. The benchmark concentration potency ranking of BDE-47 and organophosphate esters based on cytotoxicity was TDtBPP>BDMPP>TBOEP>TDCPP>TMPP>TPHP>BDE47>IPPP=BPDP=TCPP. Additionally, TM4 cell exposure to BDE-47 increased Calcein intensity (57.9 µM) and affected lysosomes (21.6 µM), while exposure to TPHP and TMPP resulted in cellular oxidative stress changes at benchmark concentration values as low as 0.01 and 0.4 µM, respectively. Overall bioactivity considerations of the chemicals on TM4 via ToxPi analyses and AED modeling further validated emerging replacements as highly potent chemicals in comparison to BPA and BDE-47. These findings demonstrate that many bisphenol and flame retardant replacements are more potent in Sertoli cells than the legacy chemical they are replacing and that phenotypic parameter assessment is an effective tool in chemical toxicity assessment. Summary Sentence In TM4 Sertoli cells, many of the chemicals that are emerging as replacements for BPA and brominated flame retardants show greater toxicity than the chemicals that they are replacing.
doi_str_mv 10.1093/biolre/ioac101
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9476221</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/biolre/ioac101</oup_id><sourcerecordid>2823840484</sourcerecordid><originalsourceid>FETCH-LOGICAL-b489t-931012ad0f319ed9adcbd55e9f40b4cc4d9780ee243b2695ab5d0d4044fb702a3</originalsourceid><addsrcrecordid>eNqFkUtP3TAQha2qVbnQblkiS11VIuBXcuMNUoUKVKLqonRt-TFJjHLtYCeV-Pe4zQW1K1bWjD-f8ZmD0DElZ5RIfm58HBOc-6gtJfQN2tCayWrLmvYt2hBCmorzhh-gw5zvCaGCM_4eHfC6lg0TfIOmG98PlY1hhjBjv9O9Dz3WQY-PGTKOHZ4HwNB1YOe_pfF5GiDEMRfK4Zh6HeI0xNLVcyHzDKmAAd99F3gXlwz4J6Q5jh5bGMf8Ab3r9Jjh4_48Qr-uvt5d3lS3P66_XX65rYxo5VxJXuww7UjHqQQntbPG1TXIThAjrBVOblsCUEwY1sham9oRJ4gQndkSpvkRulh1p8XswNliL-lRTal4TI8qaq_-vwl-UH38raTYNozRIvBpL5Diw1J8qfu4pLKYrFjLeFtmtaJQZytlU8w5QfcygRL1JyG1JqT2CZUHJ__-6wV_jqQAn1cgLtPrYqcrW_oxwGv4EwJvrwQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2823840484</pqid></control><display><type>article</type><title>High-content imaging analyses of the effects of bisphenols and organophosphate esters on TM4 mouse Sertoli cells</title><source>Oxford Journals Online</source><creator>Rajkumar, Abishankari ; Luu, Trang ; Hales, Barbara F. ; Robaire, Bernard</creator><creatorcontrib>Rajkumar, Abishankari ; Luu, Trang ; Hales, Barbara F. ; Robaire, Bernard</creatorcontrib><description>The endocrine disruptive effects of bisphenol A (BPA) and brominated flame retardants (BDE-47) have led to restrictions on their use and increased the pressure to identify safe replacements for these chemicals. Although there is evidence that some of these alternatives may be toxic to spermatogonial and Leydig cells, little is known about the toxicity of emerging replacements on Sertoli cells. We used high-content imaging to compare the effects of legacy chemicals, BPA and BDE-47, to their corresponding replacements. TM4 Sertoli cells were exposed for 48 h to each chemical (0.001–100 µM) followed by cytotoxicity and phenotypic endpoint assessment. The benchmark concentration potency ranking for bisphenols based on cytotoxicity was BPTMC &gt; bisphenol M &gt; BPAF&gt;BPF &gt; BPS &gt; BPA. Human administered equivalent dose (AED) determination ranked BPS as the most potent alternative replacement. The benchmark concentration potency ranking of BDE-47 and organophosphate esters based on cytotoxicity was TDtBPP&gt;BDMPP&gt;TBOEP&gt;TDCPP&gt;TMPP&gt;TPHP&gt;BDE47&gt;IPPP=BPDP=TCPP. Additionally, TM4 cell exposure to BDE-47 increased Calcein intensity (57.9 µM) and affected lysosomes (21.6 µM), while exposure to TPHP and TMPP resulted in cellular oxidative stress changes at benchmark concentration values as low as 0.01 and 0.4 µM, respectively. Overall bioactivity considerations of the chemicals on TM4 via ToxPi analyses and AED modeling further validated emerging replacements as highly potent chemicals in comparison to BPA and BDE-47. These findings demonstrate that many bisphenol and flame retardant replacements are more potent in Sertoli cells than the legacy chemical they are replacing and that phenotypic parameter assessment is an effective tool in chemical toxicity assessment. Summary Sentence In TM4 Sertoli cells, many of the chemicals that are emerging as replacements for BPA and brominated flame retardants show greater toxicity than the chemicals that they are replacing.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1093/biolre/ioac101</identifier><identifier>PMID: 35596243</identifier><language>eng</language><publisher>United States: Society for the Study of Reproduction</publisher><subject>Animals ; benchmark concentrations ; Benzhydryl Compounds - toxicity ; Biological activity ; Bisphenol A ; bisphenols ; Calcein ; Chemicals ; Cytotoxicity ; endocrine-disrupting chemicals ; Esters ; Flame retardants ; Flame Retardants - toxicity ; Halogenated Diphenyl Ethers ; high-content imaging ; Humans ; Leydig cells ; Lysosomes ; Male ; Mice ; organophosphate esters ; Organophosphates ; Organophosphates - chemistry ; Organophosphates - toxicity ; Oxidative stress ; Phenols ; polybrominated diphenyl ethers ; RESEARCH ARTICLE ; Sertoli Cells</subject><ispartof>Biology of reproduction, 2022-09, Vol.107 (3), p.858-868</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com journals.permissions@oup.com</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2022</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b489t-931012ad0f319ed9adcbd55e9f40b4cc4d9780ee243b2695ab5d0d4044fb702a3</citedby><cites>FETCH-LOGICAL-b489t-931012ad0f319ed9adcbd55e9f40b4cc4d9780ee243b2695ab5d0d4044fb702a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35596243$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rajkumar, Abishankari</creatorcontrib><creatorcontrib>Luu, Trang</creatorcontrib><creatorcontrib>Hales, Barbara F.</creatorcontrib><creatorcontrib>Robaire, Bernard</creatorcontrib><title>High-content imaging analyses of the effects of bisphenols and organophosphate esters on TM4 mouse Sertoli cells</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description>The endocrine disruptive effects of bisphenol A (BPA) and brominated flame retardants (BDE-47) have led to restrictions on their use and increased the pressure to identify safe replacements for these chemicals. Although there is evidence that some of these alternatives may be toxic to spermatogonial and Leydig cells, little is known about the toxicity of emerging replacements on Sertoli cells. We used high-content imaging to compare the effects of legacy chemicals, BPA and BDE-47, to their corresponding replacements. TM4 Sertoli cells were exposed for 48 h to each chemical (0.001–100 µM) followed by cytotoxicity and phenotypic endpoint assessment. The benchmark concentration potency ranking for bisphenols based on cytotoxicity was BPTMC &gt; bisphenol M &gt; BPAF&gt;BPF &gt; BPS &gt; BPA. Human administered equivalent dose (AED) determination ranked BPS as the most potent alternative replacement. The benchmark concentration potency ranking of BDE-47 and organophosphate esters based on cytotoxicity was TDtBPP&gt;BDMPP&gt;TBOEP&gt;TDCPP&gt;TMPP&gt;TPHP&gt;BDE47&gt;IPPP=BPDP=TCPP. Additionally, TM4 cell exposure to BDE-47 increased Calcein intensity (57.9 µM) and affected lysosomes (21.6 µM), while exposure to TPHP and TMPP resulted in cellular oxidative stress changes at benchmark concentration values as low as 0.01 and 0.4 µM, respectively. Overall bioactivity considerations of the chemicals on TM4 via ToxPi analyses and AED modeling further validated emerging replacements as highly potent chemicals in comparison to BPA and BDE-47. These findings demonstrate that many bisphenol and flame retardant replacements are more potent in Sertoli cells than the legacy chemical they are replacing and that phenotypic parameter assessment is an effective tool in chemical toxicity assessment. Summary Sentence In TM4 Sertoli cells, many of the chemicals that are emerging as replacements for BPA and brominated flame retardants show greater toxicity than the chemicals that they are replacing.</description><subject>Animals</subject><subject>benchmark concentrations</subject><subject>Benzhydryl Compounds - toxicity</subject><subject>Biological activity</subject><subject>Bisphenol A</subject><subject>bisphenols</subject><subject>Calcein</subject><subject>Chemicals</subject><subject>Cytotoxicity</subject><subject>endocrine-disrupting chemicals</subject><subject>Esters</subject><subject>Flame retardants</subject><subject>Flame Retardants - toxicity</subject><subject>Halogenated Diphenyl Ethers</subject><subject>high-content imaging</subject><subject>Humans</subject><subject>Leydig cells</subject><subject>Lysosomes</subject><subject>Male</subject><subject>Mice</subject><subject>organophosphate esters</subject><subject>Organophosphates</subject><subject>Organophosphates - chemistry</subject><subject>Organophosphates - toxicity</subject><subject>Oxidative stress</subject><subject>Phenols</subject><subject>polybrominated diphenyl ethers</subject><subject>RESEARCH ARTICLE</subject><subject>Sertoli Cells</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkUtP3TAQha2qVbnQblkiS11VIuBXcuMNUoUKVKLqonRt-TFJjHLtYCeV-Pe4zQW1K1bWjD-f8ZmD0DElZ5RIfm58HBOc-6gtJfQN2tCayWrLmvYt2hBCmorzhh-gw5zvCaGCM_4eHfC6lg0TfIOmG98PlY1hhjBjv9O9Dz3WQY-PGTKOHZ4HwNB1YOe_pfF5GiDEMRfK4Zh6HeI0xNLVcyHzDKmAAd99F3gXlwz4J6Q5jh5bGMf8Ab3r9Jjh4_48Qr-uvt5d3lS3P66_XX65rYxo5VxJXuww7UjHqQQntbPG1TXIThAjrBVOblsCUEwY1sham9oRJ4gQndkSpvkRulh1p8XswNliL-lRTal4TI8qaq_-vwl-UH38raTYNozRIvBpL5Diw1J8qfu4pLKYrFjLeFtmtaJQZytlU8w5QfcygRL1JyG1JqT2CZUHJ__-6wV_jqQAn1cgLtPrYqcrW_oxwGv4EwJvrwQ</recordid><startdate>20220912</startdate><enddate>20220912</enddate><creator>Rajkumar, Abishankari</creator><creator>Luu, Trang</creator><creator>Hales, Barbara F.</creator><creator>Robaire, Bernard</creator><general>Society for the Study of Reproduction</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20220912</creationdate><title>High-content imaging analyses of the effects of bisphenols and organophosphate esters on TM4 mouse Sertoli cells</title><author>Rajkumar, Abishankari ; Luu, Trang ; Hales, Barbara F. ; Robaire, Bernard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b489t-931012ad0f319ed9adcbd55e9f40b4cc4d9780ee243b2695ab5d0d4044fb702a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>benchmark concentrations</topic><topic>Benzhydryl Compounds - toxicity</topic><topic>Biological activity</topic><topic>Bisphenol A</topic><topic>bisphenols</topic><topic>Calcein</topic><topic>Chemicals</topic><topic>Cytotoxicity</topic><topic>endocrine-disrupting chemicals</topic><topic>Esters</topic><topic>Flame retardants</topic><topic>Flame Retardants - toxicity</topic><topic>Halogenated Diphenyl Ethers</topic><topic>high-content imaging</topic><topic>Humans</topic><topic>Leydig cells</topic><topic>Lysosomes</topic><topic>Male</topic><topic>Mice</topic><topic>organophosphate esters</topic><topic>Organophosphates</topic><topic>Organophosphates - chemistry</topic><topic>Organophosphates - toxicity</topic><topic>Oxidative stress</topic><topic>Phenols</topic><topic>polybrominated diphenyl ethers</topic><topic>RESEARCH ARTICLE</topic><topic>Sertoli Cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rajkumar, Abishankari</creatorcontrib><creatorcontrib>Luu, Trang</creatorcontrib><creatorcontrib>Hales, Barbara F.</creatorcontrib><creatorcontrib>Robaire, Bernard</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 Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rajkumar, Abishankari</au><au>Luu, Trang</au><au>Hales, Barbara F.</au><au>Robaire, Bernard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-content imaging analyses of the effects of bisphenols and organophosphate esters on TM4 mouse Sertoli cells</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>2022-09-12</date><risdate>2022</risdate><volume>107</volume><issue>3</issue><spage>858</spage><epage>868</epage><pages>858-868</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><abstract>The endocrine disruptive effects of bisphenol A (BPA) and brominated flame retardants (BDE-47) have led to restrictions on their use and increased the pressure to identify safe replacements for these chemicals. Although there is evidence that some of these alternatives may be toxic to spermatogonial and Leydig cells, little is known about the toxicity of emerging replacements on Sertoli cells. We used high-content imaging to compare the effects of legacy chemicals, BPA and BDE-47, to their corresponding replacements. TM4 Sertoli cells were exposed for 48 h to each chemical (0.001–100 µM) followed by cytotoxicity and phenotypic endpoint assessment. The benchmark concentration potency ranking for bisphenols based on cytotoxicity was BPTMC &gt; bisphenol M &gt; BPAF&gt;BPF &gt; BPS &gt; BPA. Human administered equivalent dose (AED) determination ranked BPS as the most potent alternative replacement. The benchmark concentration potency ranking of BDE-47 and organophosphate esters based on cytotoxicity was TDtBPP&gt;BDMPP&gt;TBOEP&gt;TDCPP&gt;TMPP&gt;TPHP&gt;BDE47&gt;IPPP=BPDP=TCPP. Additionally, TM4 cell exposure to BDE-47 increased Calcein intensity (57.9 µM) and affected lysosomes (21.6 µM), while exposure to TPHP and TMPP resulted in cellular oxidative stress changes at benchmark concentration values as low as 0.01 and 0.4 µM, respectively. Overall bioactivity considerations of the chemicals on TM4 via ToxPi analyses and AED modeling further validated emerging replacements as highly potent chemicals in comparison to BPA and BDE-47. These findings demonstrate that many bisphenol and flame retardant replacements are more potent in Sertoli cells than the legacy chemical they are replacing and that phenotypic parameter assessment is an effective tool in chemical toxicity assessment. Summary Sentence In TM4 Sertoli cells, many of the chemicals that are emerging as replacements for BPA and brominated flame retardants show greater toxicity than the chemicals that they are replacing.</abstract><cop>United States</cop><pub>Society for the Study of Reproduction</pub><pmid>35596243</pmid><doi>10.1093/biolre/ioac101</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0006-3363
ispartof Biology of reproduction, 2022-09, Vol.107 (3), p.858-868
issn 0006-3363
1529-7268
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9476221
source Oxford Journals Online
subjects Animals
benchmark concentrations
Benzhydryl Compounds - toxicity
Biological activity
Bisphenol A
bisphenols
Calcein
Chemicals
Cytotoxicity
endocrine-disrupting chemicals
Esters
Flame retardants
Flame Retardants - toxicity
Halogenated Diphenyl Ethers
high-content imaging
Humans
Leydig cells
Lysosomes
Male
Mice
organophosphate esters
Organophosphates
Organophosphates - chemistry
Organophosphates - toxicity
Oxidative stress
Phenols
polybrominated diphenyl ethers
RESEARCH ARTICLE
Sertoli Cells
title High-content imaging analyses of the effects of bisphenols and organophosphate esters on TM4 mouse Sertoli cells
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T18%3A21%3A59IST&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=High-content%20imaging%20analyses%20of%20the%20effects%20of%20bisphenols%20and%20organophosphate%20esters%20on%20TM4%20mouse%20Sertoli%20cells&rft.jtitle=Biology%20of%20reproduction&rft.au=Rajkumar,%20Abishankari&rft.date=2022-09-12&rft.volume=107&rft.issue=3&rft.spage=858&rft.epage=868&rft.pages=858-868&rft.issn=0006-3363&rft.eissn=1529-7268&rft_id=info:doi/10.1093/biolre/ioac101&rft_dat=%3Cproquest_pubme%3E2823840484%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-b489t-931012ad0f319ed9adcbd55e9f40b4cc4d9780ee243b2695ab5d0d4044fb702a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2823840484&rft_id=info:pmid/35596243&rft_oup_id=10.1093/biolre/ioac101&rfr_iscdi=true