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...
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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 |
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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 & 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 & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & 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> |
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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 |
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