Modeling Environmentally-Induced Motor Neuron Degeneration in Zebrafish

Zebrafish have been used to investigate motor neuron degeneration, including as a model system to examine the pathogenesis of amyotrophic lateral sclerosis (ALS). The use of zebrafish for this purpose has some advantages over other in vivo model systems. In the current paper, we show that bisphenol...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Scientific reports 2018-03, Vol.8 (1), p.4890-11, Article 4890
Hauptverfasser: Morrice, Jessica R., Gregory-Evans, Cheryl Y., Shaw, Christopher A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 11
container_issue 1
container_start_page 4890
container_title Scientific reports
container_volume 8
creator Morrice, Jessica R.
Gregory-Evans, Cheryl Y.
Shaw, Christopher A.
description Zebrafish have been used to investigate motor neuron degeneration, including as a model system to examine the pathogenesis of amyotrophic lateral sclerosis (ALS). The use of zebrafish for this purpose has some advantages over other in vivo model systems. In the current paper, we show that bisphenol A (BPA) exposure in zebrafish embryos results in motor neuron degeneration with affected motor function, reduced motor axon length and branching, reduced neuromuscular junction integrity, motor neuron cell death and the presence of activated microglia. In zebrafish, motor axon length is the conventional method for estimating motor neuron degeneration, yet this measurement has not been confirmed as a valid surrogate marker. We also show that reduced motor axon length as measured from the sagittal plane is correlated with increased motor neuron cell death. Our preliminary timeline studies suggest that axonopathy precedes motor cell death. This outcome may have implications for early phase treatments of motor neuron degeneration.
doi_str_mv 10.1038/s41598-018-23018-w
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5861069</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2016533512</sourcerecordid><originalsourceid>FETCH-LOGICAL-c540t-2e53f5174aed0f8622e988017e4b38e7bba519b32550811f377cf12d2e3dcd253</originalsourceid><addsrcrecordid>eNp9kblOxDAQhi0EAgS8AAWKREMT8JFJ7AYJcUscDTQ0lpNMFqOsDXYC4u3xstwFLuwZzTe_Z_QTssnoLqNC7sWCgZI5ZTLnYna_LJBVTgtIKeeLP-IVshHjA00HuCqYWiYrXAGosoBVcnrpW-ytm2TH7tkG76boBtP3r_m5a8cG2-zSDz5kVzimYnaEE3QYzGBTYl12h3UwnY3362SpM33EjY93jdyeHN8cnuUX16fnhwcXeQMFHXKOIDpgVWGwpZ0sOUclJWUVFrWQWNW1AaZqwQGoZKwTVdV0jLccRdu0HMQa2Z_rPo71FNsmTRtMrx-DnZrwqr2x-nfF2Xs98c8aZMloqZLAzodA8E8jxkFPbWyw741DP0bNKStBCGA8odt_0Ac_BpfWm1GQ5lOySBSfU03wMQbsvoZhVM-s0nOrdDJJv1ulX1LT1s81vlo-jUmAmAMxldwEw_ff_8i-AZabn4E</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2015811984</pqid></control><display><type>article</type><title>Modeling Environmentally-Induced Motor Neuron Degeneration in Zebrafish</title><source>DOAJ Directory of Open Access Journals</source><source>Springer Nature OA Free Journals</source><source>Nature Free</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Morrice, Jessica R. ; Gregory-Evans, Cheryl Y. ; Shaw, Christopher A.</creator><creatorcontrib>Morrice, Jessica R. ; Gregory-Evans, Cheryl Y. ; Shaw, Christopher A.</creatorcontrib><description>Zebrafish have been used to investigate motor neuron degeneration, including as a model system to examine the pathogenesis of amyotrophic lateral sclerosis (ALS). The use of zebrafish for this purpose has some advantages over other in vivo model systems. In the current paper, we show that bisphenol A (BPA) exposure in zebrafish embryos results in motor neuron degeneration with affected motor function, reduced motor axon length and branching, reduced neuromuscular junction integrity, motor neuron cell death and the presence of activated microglia. In zebrafish, motor axon length is the conventional method for estimating motor neuron degeneration, yet this measurement has not been confirmed as a valid surrogate marker. We also show that reduced motor axon length as measured from the sagittal plane is correlated with increased motor neuron cell death. Our preliminary timeline studies suggest that axonopathy precedes motor cell death. This outcome may have implications for early phase treatments of motor neuron degeneration.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-018-23018-w</identifier><identifier>PMID: 29559645</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/51 ; 14/1 ; 14/19 ; 14/35 ; 14/5 ; 631/378/1689/1285 ; 631/378/1934 ; 631/378/371 ; 64/116 ; Amyotrophic lateral sclerosis ; Apoptosis ; Bisphenol A ; Cell death ; Danio rerio ; Degeneration ; Embryos ; Humanities and Social Sciences ; Microglia ; Mortality ; multidisciplinary ; Science ; Science (multidisciplinary)</subject><ispartof>Scientific reports, 2018-03, Vol.8 (1), p.4890-11, Article 4890</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-2e53f5174aed0f8622e988017e4b38e7bba519b32550811f377cf12d2e3dcd253</citedby><cites>FETCH-LOGICAL-c540t-2e53f5174aed0f8622e988017e4b38e7bba519b32550811f377cf12d2e3dcd253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861069/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5861069/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27923,27924,41119,42188,51575,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29559645$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morrice, Jessica R.</creatorcontrib><creatorcontrib>Gregory-Evans, Cheryl Y.</creatorcontrib><creatorcontrib>Shaw, Christopher A.</creatorcontrib><title>Modeling Environmentally-Induced Motor Neuron Degeneration in Zebrafish</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Zebrafish have been used to investigate motor neuron degeneration, including as a model system to examine the pathogenesis of amyotrophic lateral sclerosis (ALS). The use of zebrafish for this purpose has some advantages over other in vivo model systems. In the current paper, we show that bisphenol A (BPA) exposure in zebrafish embryos results in motor neuron degeneration with affected motor function, reduced motor axon length and branching, reduced neuromuscular junction integrity, motor neuron cell death and the presence of activated microglia. In zebrafish, motor axon length is the conventional method for estimating motor neuron degeneration, yet this measurement has not been confirmed as a valid surrogate marker. We also show that reduced motor axon length as measured from the sagittal plane is correlated with increased motor neuron cell death. Our preliminary timeline studies suggest that axonopathy precedes motor cell death. This outcome may have implications for early phase treatments of motor neuron degeneration.</description><subject>13/51</subject><subject>14/1</subject><subject>14/19</subject><subject>14/35</subject><subject>14/5</subject><subject>631/378/1689/1285</subject><subject>631/378/1934</subject><subject>631/378/371</subject><subject>64/116</subject><subject>Amyotrophic lateral sclerosis</subject><subject>Apoptosis</subject><subject>Bisphenol A</subject><subject>Cell death</subject><subject>Danio rerio</subject><subject>Degeneration</subject><subject>Embryos</subject><subject>Humanities and Social Sciences</subject><subject>Microglia</subject><subject>Mortality</subject><subject>multidisciplinary</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kblOxDAQhi0EAgS8AAWKREMT8JFJ7AYJcUscDTQ0lpNMFqOsDXYC4u3xstwFLuwZzTe_Z_QTssnoLqNC7sWCgZI5ZTLnYna_LJBVTgtIKeeLP-IVshHjA00HuCqYWiYrXAGosoBVcnrpW-ytm2TH7tkG76boBtP3r_m5a8cG2-zSDz5kVzimYnaEE3QYzGBTYl12h3UwnY3362SpM33EjY93jdyeHN8cnuUX16fnhwcXeQMFHXKOIDpgVWGwpZ0sOUclJWUVFrWQWNW1AaZqwQGoZKwTVdV0jLccRdu0HMQa2Z_rPo71FNsmTRtMrx-DnZrwqr2x-nfF2Xs98c8aZMloqZLAzodA8E8jxkFPbWyw741DP0bNKStBCGA8odt_0Ac_BpfWm1GQ5lOySBSfU03wMQbsvoZhVM-s0nOrdDJJv1ulX1LT1s81vlo-jUmAmAMxldwEw_ff_8i-AZabn4E</recordid><startdate>20180320</startdate><enddate>20180320</enddate><creator>Morrice, Jessica R.</creator><creator>Gregory-Evans, Cheryl Y.</creator><creator>Shaw, Christopher A.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</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>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180320</creationdate><title>Modeling Environmentally-Induced Motor Neuron Degeneration in Zebrafish</title><author>Morrice, Jessica R. ; Gregory-Evans, Cheryl Y. ; Shaw, Christopher A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-2e53f5174aed0f8622e988017e4b38e7bba519b32550811f377cf12d2e3dcd253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>13/51</topic><topic>14/1</topic><topic>14/19</topic><topic>14/35</topic><topic>14/5</topic><topic>631/378/1689/1285</topic><topic>631/378/1934</topic><topic>631/378/371</topic><topic>64/116</topic><topic>Amyotrophic lateral sclerosis</topic><topic>Apoptosis</topic><topic>Bisphenol A</topic><topic>Cell death</topic><topic>Danio rerio</topic><topic>Degeneration</topic><topic>Embryos</topic><topic>Humanities and Social Sciences</topic><topic>Microglia</topic><topic>Mortality</topic><topic>multidisciplinary</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morrice, Jessica R.</creatorcontrib><creatorcontrib>Gregory-Evans, Cheryl Y.</creatorcontrib><creatorcontrib>Shaw, Christopher A.</creatorcontrib><collection>Springer Nature OA Free Journals</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>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</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>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morrice, Jessica R.</au><au>Gregory-Evans, Cheryl Y.</au><au>Shaw, Christopher A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modeling Environmentally-Induced Motor Neuron Degeneration in Zebrafish</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2018-03-20</date><risdate>2018</risdate><volume>8</volume><issue>1</issue><spage>4890</spage><epage>11</epage><pages>4890-11</pages><artnum>4890</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Zebrafish have been used to investigate motor neuron degeneration, including as a model system to examine the pathogenesis of amyotrophic lateral sclerosis (ALS). The use of zebrafish for this purpose has some advantages over other in vivo model systems. In the current paper, we show that bisphenol A (BPA) exposure in zebrafish embryos results in motor neuron degeneration with affected motor function, reduced motor axon length and branching, reduced neuromuscular junction integrity, motor neuron cell death and the presence of activated microglia. In zebrafish, motor axon length is the conventional method for estimating motor neuron degeneration, yet this measurement has not been confirmed as a valid surrogate marker. We also show that reduced motor axon length as measured from the sagittal plane is correlated with increased motor neuron cell death. Our preliminary timeline studies suggest that axonopathy precedes motor cell death. This outcome may have implications for early phase treatments of motor neuron degeneration.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29559645</pmid><doi>10.1038/s41598-018-23018-w</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2045-2322
ispartof Scientific reports, 2018-03, Vol.8 (1), p.4890-11, Article 4890
issn 2045-2322
2045-2322
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5861069
source DOAJ Directory of Open Access Journals; Springer Nature OA Free Journals; Nature Free; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry
subjects 13/51
14/1
14/19
14/35
14/5
631/378/1689/1285
631/378/1934
631/378/371
64/116
Amyotrophic lateral sclerosis
Apoptosis
Bisphenol A
Cell death
Danio rerio
Degeneration
Embryos
Humanities and Social Sciences
Microglia
Mortality
multidisciplinary
Science
Science (multidisciplinary)
title Modeling Environmentally-Induced Motor Neuron Degeneration in Zebrafish
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T09%3A46%3A56IST&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=Modeling%20Environmentally-Induced%20Motor%20Neuron%20Degeneration%20in%20Zebrafish&rft.jtitle=Scientific%20reports&rft.au=Morrice,%20Jessica%20R.&rft.date=2018-03-20&rft.volume=8&rft.issue=1&rft.spage=4890&rft.epage=11&rft.pages=4890-11&rft.artnum=4890&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/s41598-018-23018-w&rft_dat=%3Cproquest_pubme%3E2016533512%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=2015811984&rft_id=info:pmid/29559645&rfr_iscdi=true