Caspases and matrix metalloproteases facilitate collective behavior of non-neural ectoderm after hindbrain neuropore closure

Mammalian brain is formed through neural tube closure (NTC), wherein both ridges of opposing neural folds are fused in the midline and remodeled in the roof plate of the neural tube and overlying non-neural ectodermal layer. Apoptosis is widely observed from the beginning of NTC at the neural ridges...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:BMC developmental biology 2018-07, Vol.18 (1), p.17-17, Article 17
Hauptverfasser: Shinotsuka, Naomi, Yamaguchi, Yoshifumi, Nakazato, Kenichi, Matsumoto, Yudai, Mochizuki, Atsushi, Miura, Masayuki
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 17
container_issue 1
container_start_page 17
container_title BMC developmental biology
container_volume 18
creator Shinotsuka, Naomi
Yamaguchi, Yoshifumi
Nakazato, Kenichi
Matsumoto, Yudai
Mochizuki, Atsushi
Miura, Masayuki
description Mammalian brain is formed through neural tube closure (NTC), wherein both ridges of opposing neural folds are fused in the midline and remodeled in the roof plate of the neural tube and overlying non-neural ectodermal layer. Apoptosis is widely observed from the beginning of NTC at the neural ridges and is crucial for the proper progression of NTC, but its role after the closure remains less clear. Here, we conducted live-imaging analysis of the mid-hindbrain neuropore (MHNP) closure and revealed unexpected collective behavior of cells surrounding the MHNP. The cells first gathered to the closing point and subsequently relocated as if they were released from the point. Inhibition of caspases or matrix metalloproteases with chemical inhibitors impaired the cell relocation. These lines of evidence suggest that apoptosis-mediated degradation of extracellular matrix might facilitate the final process of neuropore closure.
doi_str_mv 10.1186/s12861-018-0175-3
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6069860</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A556986561</galeid><sourcerecordid>A556986561</sourcerecordid><originalsourceid>FETCH-LOGICAL-c638t-a9785bfa357042a4fd78605bf7324c9fcab8e48c1011eae6dda3ea7f6d4b23e13</originalsourceid><addsrcrecordid>eNptkk2LFDEQhhtR3HX1B3iRgBc99Jp00unMRVgGPxYWBD_AW6hOV89kSSdjkh5W8MebdtZlRySEhKqn3qqEt6qeM3rOmJJvEmuUZDVlquyurfmD6pSJjtUN498f3rufVE9SuqYFUkw-rk44pVJwKU6rX2tIO0iYCPiBTJCjvSETZnAu7GLI-Cc3grHOZshITHAOTbZ7JD1uYW9DJGEkPvja4xzBkZINA8aJwJgxkq31Qx_BerLkwy7EIuJCmiM-rR6N4BI-uz3Pqm_v331df6yvPn24XF9c1UZylWtYdartR-BtR0UDYhw6JWmJdLwRZjUa6BUKZRhlDAHlMABH6EY5iL7hyPhZ9fagu5v7CQeDPpdB9S7aCeJPHcDq44y3W70Jey2pXJVWReDVrUAMP2ZMWU82GXQOPIY56YYq1oqupW1BX_6DXoc5-vK8Qq2oEI0S96gNONTWj6H0NYuovmjbpWkrl7nP_0OVNeBkTfA42hI_Knh9VFCYjDd5A3NK-vLL52OWHVgTQ0oRx7v_YFQv9tIHe-liL73YS_NS8-L-R95V_PUT_w0RgM0i</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2090442845</pqid></control><display><type>article</type><title>Caspases and matrix metalloproteases facilitate collective behavior of non-neural ectoderm after hindbrain neuropore closure</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central Open Access</source><source>Springer Nature OA Free Journals</source><source>BioMedCentral</source><source>PubMed Central</source><creator>Shinotsuka, Naomi ; Yamaguchi, Yoshifumi ; Nakazato, Kenichi ; Matsumoto, Yudai ; Mochizuki, Atsushi ; Miura, Masayuki</creator><creatorcontrib>Shinotsuka, Naomi ; Yamaguchi, Yoshifumi ; Nakazato, Kenichi ; Matsumoto, Yudai ; Mochizuki, Atsushi ; Miura, Masayuki</creatorcontrib><description>Mammalian brain is formed through neural tube closure (NTC), wherein both ridges of opposing neural folds are fused in the midline and remodeled in the roof plate of the neural tube and overlying non-neural ectodermal layer. Apoptosis is widely observed from the beginning of NTC at the neural ridges and is crucial for the proper progression of NTC, but its role after the closure remains less clear. Here, we conducted live-imaging analysis of the mid-hindbrain neuropore (MHNP) closure and revealed unexpected collective behavior of cells surrounding the MHNP. The cells first gathered to the closing point and subsequently relocated as if they were released from the point. Inhibition of caspases or matrix metalloproteases with chemical inhibitors impaired the cell relocation. These lines of evidence suggest that apoptosis-mediated degradation of extracellular matrix might facilitate the final process of neuropore closure.</description><identifier>ISSN: 1471-213X</identifier><identifier>EISSN: 1471-213X</identifier><identifier>DOI: 10.1186/s12861-018-0175-3</identifier><identifier>PMID: 30064364</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Amino Acid Chloromethyl Ketones - pharmacology ; Animals ; Apoptosis ; Caspases ; Caspases - metabolism ; Cell regulation ; Cell Shape - drug effects ; Chemical properties ; Cytological research ; Ectoderm ; Ectoderm - cytology ; Ectoderm - embryology ; Ectoderm - enzymology ; Extracellular matrix ; Hindbrain ; Insects ; Mammals ; Matrix Metalloproteinases - metabolism ; Mice, Transgenic ; Morphogenesis ; Morphology ; Movement ; Neural Crest - embryology ; Neural tube ; Neural Tube - cytology ; Neural Tube - embryology ; Neuroimaging ; Properties ; Proteases ; Relocation ; Rhombencephalon - embryology</subject><ispartof>BMC developmental biology, 2018-07, Vol.18 (1), p.17-17, Article 17</ispartof><rights>COPYRIGHT 2018 BioMed Central Ltd.</rights><rights>Copyright © 2018. This work is licensed 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><rights>The Author(s). 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c638t-a9785bfa357042a4fd78605bf7324c9fcab8e48c1011eae6dda3ea7f6d4b23e13</citedby><cites>FETCH-LOGICAL-c638t-a9785bfa357042a4fd78605bf7324c9fcab8e48c1011eae6dda3ea7f6d4b23e13</cites><orcidid>0000-0001-7340-4557</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/PMC6069860/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069860/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30064364$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shinotsuka, Naomi</creatorcontrib><creatorcontrib>Yamaguchi, Yoshifumi</creatorcontrib><creatorcontrib>Nakazato, Kenichi</creatorcontrib><creatorcontrib>Matsumoto, Yudai</creatorcontrib><creatorcontrib>Mochizuki, Atsushi</creatorcontrib><creatorcontrib>Miura, Masayuki</creatorcontrib><title>Caspases and matrix metalloproteases facilitate collective behavior of non-neural ectoderm after hindbrain neuropore closure</title><title>BMC developmental biology</title><addtitle>BMC Dev Biol</addtitle><description>Mammalian brain is formed through neural tube closure (NTC), wherein both ridges of opposing neural folds are fused in the midline and remodeled in the roof plate of the neural tube and overlying non-neural ectodermal layer. Apoptosis is widely observed from the beginning of NTC at the neural ridges and is crucial for the proper progression of NTC, but its role after the closure remains less clear. Here, we conducted live-imaging analysis of the mid-hindbrain neuropore (MHNP) closure and revealed unexpected collective behavior of cells surrounding the MHNP. The cells first gathered to the closing point and subsequently relocated as if they were released from the point. Inhibition of caspases or matrix metalloproteases with chemical inhibitors impaired the cell relocation. These lines of evidence suggest that apoptosis-mediated degradation of extracellular matrix might facilitate the final process of neuropore closure.</description><subject>Amino Acid Chloromethyl Ketones - pharmacology</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Caspases</subject><subject>Caspases - metabolism</subject><subject>Cell regulation</subject><subject>Cell Shape - drug effects</subject><subject>Chemical properties</subject><subject>Cytological research</subject><subject>Ectoderm</subject><subject>Ectoderm - cytology</subject><subject>Ectoderm - embryology</subject><subject>Ectoderm - enzymology</subject><subject>Extracellular matrix</subject><subject>Hindbrain</subject><subject>Insects</subject><subject>Mammals</subject><subject>Matrix Metalloproteinases - metabolism</subject><subject>Mice, Transgenic</subject><subject>Morphogenesis</subject><subject>Morphology</subject><subject>Movement</subject><subject>Neural Crest - embryology</subject><subject>Neural tube</subject><subject>Neural Tube - cytology</subject><subject>Neural Tube - embryology</subject><subject>Neuroimaging</subject><subject>Properties</subject><subject>Proteases</subject><subject>Relocation</subject><subject>Rhombencephalon - embryology</subject><issn>1471-213X</issn><issn>1471-213X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptkk2LFDEQhhtR3HX1B3iRgBc99Jp00unMRVgGPxYWBD_AW6hOV89kSSdjkh5W8MebdtZlRySEhKqn3qqEt6qeM3rOmJJvEmuUZDVlquyurfmD6pSJjtUN498f3rufVE9SuqYFUkw-rk44pVJwKU6rX2tIO0iYCPiBTJCjvSETZnAu7GLI-Cc3grHOZshITHAOTbZ7JD1uYW9DJGEkPvja4xzBkZINA8aJwJgxkq31Qx_BerLkwy7EIuJCmiM-rR6N4BI-uz3Pqm_v331df6yvPn24XF9c1UZylWtYdartR-BtR0UDYhw6JWmJdLwRZjUa6BUKZRhlDAHlMABH6EY5iL7hyPhZ9fagu5v7CQeDPpdB9S7aCeJPHcDq44y3W70Jey2pXJVWReDVrUAMP2ZMWU82GXQOPIY56YYq1oqupW1BX_6DXoc5-vK8Qq2oEI0S96gNONTWj6H0NYuovmjbpWkrl7nP_0OVNeBkTfA42hI_Knh9VFCYjDd5A3NK-vLL52OWHVgTQ0oRx7v_YFQv9tIHe-liL73YS_NS8-L-R95V_PUT_w0RgM0i</recordid><startdate>20180731</startdate><enddate>20180731</enddate><creator>Shinotsuka, Naomi</creator><creator>Yamaguchi, Yoshifumi</creator><creator>Nakazato, Kenichi</creator><creator>Matsumoto, Yudai</creator><creator>Mochizuki, Atsushi</creator><creator>Miura, Masayuki</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>ISR</scope><scope>3V.</scope><scope>7SS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</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>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>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7340-4557</orcidid></search><sort><creationdate>20180731</creationdate><title>Caspases and matrix metalloproteases facilitate collective behavior of non-neural ectoderm after hindbrain neuropore closure</title><author>Shinotsuka, Naomi ; Yamaguchi, Yoshifumi ; Nakazato, Kenichi ; Matsumoto, Yudai ; Mochizuki, Atsushi ; Miura, Masayuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c638t-a9785bfa357042a4fd78605bf7324c9fcab8e48c1011eae6dda3ea7f6d4b23e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Amino Acid Chloromethyl Ketones - pharmacology</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Caspases</topic><topic>Caspases - metabolism</topic><topic>Cell regulation</topic><topic>Cell Shape - drug effects</topic><topic>Chemical properties</topic><topic>Cytological research</topic><topic>Ectoderm</topic><topic>Ectoderm - cytology</topic><topic>Ectoderm - embryology</topic><topic>Ectoderm - enzymology</topic><topic>Extracellular matrix</topic><topic>Hindbrain</topic><topic>Insects</topic><topic>Mammals</topic><topic>Matrix Metalloproteinases - metabolism</topic><topic>Mice, Transgenic</topic><topic>Morphogenesis</topic><topic>Morphology</topic><topic>Movement</topic><topic>Neural Crest - embryology</topic><topic>Neural tube</topic><topic>Neural Tube - cytology</topic><topic>Neural Tube - embryology</topic><topic>Neuroimaging</topic><topic>Properties</topic><topic>Proteases</topic><topic>Relocation</topic><topic>Rhombencephalon - embryology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shinotsuka, Naomi</creatorcontrib><creatorcontrib>Yamaguchi, Yoshifumi</creatorcontrib><creatorcontrib>Nakazato, Kenichi</creatorcontrib><creatorcontrib>Matsumoto, Yudai</creatorcontrib><creatorcontrib>Mochizuki, Atsushi</creatorcontrib><creatorcontrib>Miura, Masayuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical 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 Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>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 China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shinotsuka, Naomi</au><au>Yamaguchi, Yoshifumi</au><au>Nakazato, Kenichi</au><au>Matsumoto, Yudai</au><au>Mochizuki, Atsushi</au><au>Miura, Masayuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Caspases and matrix metalloproteases facilitate collective behavior of non-neural ectoderm after hindbrain neuropore closure</atitle><jtitle>BMC developmental biology</jtitle><addtitle>BMC Dev Biol</addtitle><date>2018-07-31</date><risdate>2018</risdate><volume>18</volume><issue>1</issue><spage>17</spage><epage>17</epage><pages>17-17</pages><artnum>17</artnum><issn>1471-213X</issn><eissn>1471-213X</eissn><abstract>Mammalian brain is formed through neural tube closure (NTC), wherein both ridges of opposing neural folds are fused in the midline and remodeled in the roof plate of the neural tube and overlying non-neural ectodermal layer. Apoptosis is widely observed from the beginning of NTC at the neural ridges and is crucial for the proper progression of NTC, but its role after the closure remains less clear. Here, we conducted live-imaging analysis of the mid-hindbrain neuropore (MHNP) closure and revealed unexpected collective behavior of cells surrounding the MHNP. The cells first gathered to the closing point and subsequently relocated as if they were released from the point. Inhibition of caspases or matrix metalloproteases with chemical inhibitors impaired the cell relocation. These lines of evidence suggest that apoptosis-mediated degradation of extracellular matrix might facilitate the final process of neuropore closure.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>30064364</pmid><doi>10.1186/s12861-018-0175-3</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-7340-4557</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1471-213X
ispartof BMC developmental biology, 2018-07, Vol.18 (1), p.17-17, Article 17
issn 1471-213X
1471-213X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6069860
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Springer Nature OA Free Journals; BioMedCentral; PubMed Central
subjects Amino Acid Chloromethyl Ketones - pharmacology
Animals
Apoptosis
Caspases
Caspases - metabolism
Cell regulation
Cell Shape - drug effects
Chemical properties
Cytological research
Ectoderm
Ectoderm - cytology
Ectoderm - embryology
Ectoderm - enzymology
Extracellular matrix
Hindbrain
Insects
Mammals
Matrix Metalloproteinases - metabolism
Mice, Transgenic
Morphogenesis
Morphology
Movement
Neural Crest - embryology
Neural tube
Neural Tube - cytology
Neural Tube - embryology
Neuroimaging
Properties
Proteases
Relocation
Rhombencephalon - embryology
title Caspases and matrix metalloproteases facilitate collective behavior of non-neural ectoderm after hindbrain neuropore closure
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T20%3A14%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Caspases%20and%20matrix%20metalloproteases%20facilitate%20collective%20behavior%20of%20non-neural%20ectoderm%20after%20hindbrain%20neuropore%20closure&rft.jtitle=BMC%20developmental%20biology&rft.au=Shinotsuka,%20Naomi&rft.date=2018-07-31&rft.volume=18&rft.issue=1&rft.spage=17&rft.epage=17&rft.pages=17-17&rft.artnum=17&rft.issn=1471-213X&rft.eissn=1471-213X&rft_id=info:doi/10.1186/s12861-018-0175-3&rft_dat=%3Cgale_pubme%3EA556986561%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2090442845&rft_id=info:pmid/30064364&rft_galeid=A556986561&rfr_iscdi=true