Transdifferentiation and mesenchymal‐to‐epithelial transition during regeneration in Demospongiae (Porifera)

Origin and early evolution of regeneration mechanisms remain among the most pressing questions in animal regeneration biology. Porifera have exceptional regenerative capacities and, as early Metazoan lineage, are a promising model for studying evolutionary aspects of regeneration. Here, we focus on...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of experimental zoology. Part B, Molecular and developmental evolution Molecular and developmental evolution, 2020-01, Vol.334 (1), p.37-58
Hauptverfasser: Ereskovsky, Alexander V., Tokina, Daria B., Saidov, Danial M., Baghdiguian, Stephen, Le Goff, Emilie, Lavrov, Andrey I.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 58
container_issue 1
container_start_page 37
container_title Journal of experimental zoology. Part B, Molecular and developmental evolution
container_volume 334
creator Ereskovsky, Alexander V.
Tokina, Daria B.
Saidov, Danial M.
Baghdiguian, Stephen
Le Goff, Emilie
Lavrov, Andrey I.
description Origin and early evolution of regeneration mechanisms remain among the most pressing questions in animal regeneration biology. Porifera have exceptional regenerative capacities and, as early Metazoan lineage, are a promising model for studying evolutionary aspects of regeneration. Here, we focus on reparative regeneration of the body wall in the Mediterranean demosponge Aplysina cavernicola. The epithelialization of the wound surface is completed within 2 days, and the wound is completely healed within 2 weeks. The regeneration is accompanied with the formation of a mass of undifferentiated cells (blastema), which consists of archaeocytes, dedifferentiated choanocytes, anucleated amoebocytes, and differentiated spherulous cells. The main mechanisms of A. cavernicola regeneration are cell dedifferentiation with active migration and subsequent redifferentiation or transdifferentiation of polypotent cells through the mesenchymal‐to‐epithelial transformation. The main cell sources of the regeneration are archaeocytes and choanocytes. At early stages of the regeneration, the blastema almost devoid of cell proliferation, but after 24 hr postoperation (hpo) and up to 72 hpo numerous DNA‐synthesizing cells appear there. In contrast to intact tissues, where vast majority of DNA‐synthesizing cells are choanocytes, all 5‐ethynyl‐2′‐deoxyuridine‐labeled cells in the blastema are mesohyl cells. Intact tissues, distant from the wound, retains intact level of cell proliferation during whole regeneration process. For the first time, the apoptosis was studied during the regeneration of sponges. Two waves of apoptosis were detected during A. cavernicola regeneration: The first wave at 6–12 hpo and the second wave at 48–72 hpo. The epithelialization of the wound in the demosponge Aplysina cavernicola is completed within 2 days, and the wound is completely healed within 2 weeks. The regeneration is accompanied with the formation of a blastema, consisting of archaeocytes, dedifferentiated choanocytes, and other cells. The main mechanisms of regeneration are cell dedifferentiation with subsequent transdifferentiation of cells through the mesenchymal‐to‐epithelial transformation. Research Highlights Regeneration in Aplysina cavernicola is accompanied with the formation of a blastema, cell dedifferentiation and re‐ or transdifferentiation through the mesenchymal‐to‐epithelial transformation. Apoptosis participate in regeneration.
doi_str_mv 10.1002/jez.b.22919
format Article
fullrecord <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_02354341v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2314574361</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4039-6bf648eb342b1f660ebd9179795b926b1071238808b7aece033687818ae051b03</originalsourceid><addsrcrecordid>eNp9kb9u2zAQh4kgRZ24nboXGmMEdnikqD9j4iRNCwPpkC5dCFI62TQkUiHlFs6UR8gz5kkqW4nHLjzi8N13wP0I-QJ0BpSyizU-zfSMsRzyI3ICQrCpoCCOD3-ajshpCOseTqgQH8mIQ8oE5PEJaR-8sqE0VYUebWdUZ5yNlC2jBgPaYrVtVP36_NK5_sHWdCusjaqjbjdm9nC58cYuI49LtOgHgbHRNTYutM4ujcLo7Kfzpl-hJp_Ih0rVAT-_1TH5dXvzML-bLu6_fZ9fLqZFTHk-TXSVxBlqHjMNVZJQ1GUOaZ7mQucs0UBTYDzLaKZThQVSzpMszSBTSAVoysdkMnhXqpatN43yW-mUkXeXC7nrUcZFzGP4Az17NrCtd48bDJ1sTCiwrpVFtwmScYhFGvNkh54PaOFdCB6rgxuo3MUh-ziklvs4evrrm3ijGywP7Pv9e4ANwF9T4_Z_Lvnj5vfVYP0H19iYKQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2314574361</pqid></control><display><type>article</type><title>Transdifferentiation and mesenchymal‐to‐epithelial transition during regeneration in Demospongiae (Porifera)</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Ereskovsky, Alexander V. ; Tokina, Daria B. ; Saidov, Danial M. ; Baghdiguian, Stephen ; Le Goff, Emilie ; Lavrov, Andrey I.</creator><creatorcontrib>Ereskovsky, Alexander V. ; Tokina, Daria B. ; Saidov, Danial M. ; Baghdiguian, Stephen ; Le Goff, Emilie ; Lavrov, Andrey I.</creatorcontrib><description>Origin and early evolution of regeneration mechanisms remain among the most pressing questions in animal regeneration biology. Porifera have exceptional regenerative capacities and, as early Metazoan lineage, are a promising model for studying evolutionary aspects of regeneration. Here, we focus on reparative regeneration of the body wall in the Mediterranean demosponge Aplysina cavernicola. The epithelialization of the wound surface is completed within 2 days, and the wound is completely healed within 2 weeks. The regeneration is accompanied with the formation of a mass of undifferentiated cells (blastema), which consists of archaeocytes, dedifferentiated choanocytes, anucleated amoebocytes, and differentiated spherulous cells. The main mechanisms of A. cavernicola regeneration are cell dedifferentiation with active migration and subsequent redifferentiation or transdifferentiation of polypotent cells through the mesenchymal‐to‐epithelial transformation. The main cell sources of the regeneration are archaeocytes and choanocytes. At early stages of the regeneration, the blastema almost devoid of cell proliferation, but after 24 hr postoperation (hpo) and up to 72 hpo numerous DNA‐synthesizing cells appear there. In contrast to intact tissues, where vast majority of DNA‐synthesizing cells are choanocytes, all 5‐ethynyl‐2′‐deoxyuridine‐labeled cells in the blastema are mesohyl cells. Intact tissues, distant from the wound, retains intact level of cell proliferation during whole regeneration process. For the first time, the apoptosis was studied during the regeneration of sponges. Two waves of apoptosis were detected during A. cavernicola regeneration: The first wave at 6–12 hpo and the second wave at 48–72 hpo. The epithelialization of the wound in the demosponge Aplysina cavernicola is completed within 2 days, and the wound is completely healed within 2 weeks. The regeneration is accompanied with the formation of a blastema, consisting of archaeocytes, dedifferentiated choanocytes, and other cells. The main mechanisms of regeneration are cell dedifferentiation with subsequent transdifferentiation of cells through the mesenchymal‐to‐epithelial transformation. Research Highlights Regeneration in Aplysina cavernicola is accompanied with the formation of a blastema, cell dedifferentiation and re‐ or transdifferentiation through the mesenchymal‐to‐epithelial transformation. Apoptosis participate in regeneration.</description><identifier>ISSN: 1552-5007</identifier><identifier>EISSN: 1552-5015</identifier><identifier>DOI: 10.1002/jez.b.22919</identifier><identifier>PMID: 31725194</identifier><language>eng</language><publisher>United States: Wiley</publisher><subject>Animals ; apoptosis ; blastema ; Cell Differentiation ; Cell Transdifferentiation - physiology ; demosponges ; Development Biology ; Embryology and Organogenesis ; Life Sciences ; mesenchymal‐to‐epithelial transformation ; Morphogenesis ; Porifera - cytology ; Porifera - physiology ; Regeneration ; transdifferentiation</subject><ispartof>Journal of experimental zoology. Part B, Molecular and developmental evolution, 2020-01, Vol.334 (1), p.37-58</ispartof><rights>2019 Wiley Periodicals, Inc.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4039-6bf648eb342b1f660ebd9179795b926b1071238808b7aece033687818ae051b03</citedby><cites>FETCH-LOGICAL-c4039-6bf648eb342b1f660ebd9179795b926b1071238808b7aece033687818ae051b03</cites><orcidid>0000-0003-1079-7204 ; 0000-0002-2992-9708 ; 0000-0002-0788-9039</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjez.b.22919$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjez.b.22919$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,4024,27923,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31725194$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02354341$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Ereskovsky, Alexander V.</creatorcontrib><creatorcontrib>Tokina, Daria B.</creatorcontrib><creatorcontrib>Saidov, Danial M.</creatorcontrib><creatorcontrib>Baghdiguian, Stephen</creatorcontrib><creatorcontrib>Le Goff, Emilie</creatorcontrib><creatorcontrib>Lavrov, Andrey I.</creatorcontrib><title>Transdifferentiation and mesenchymal‐to‐epithelial transition during regeneration in Demospongiae (Porifera)</title><title>Journal of experimental zoology. Part B, Molecular and developmental evolution</title><addtitle>J Exp Zool B Mol Dev Evol</addtitle><description>Origin and early evolution of regeneration mechanisms remain among the most pressing questions in animal regeneration biology. Porifera have exceptional regenerative capacities and, as early Metazoan lineage, are a promising model for studying evolutionary aspects of regeneration. Here, we focus on reparative regeneration of the body wall in the Mediterranean demosponge Aplysina cavernicola. The epithelialization of the wound surface is completed within 2 days, and the wound is completely healed within 2 weeks. The regeneration is accompanied with the formation of a mass of undifferentiated cells (blastema), which consists of archaeocytes, dedifferentiated choanocytes, anucleated amoebocytes, and differentiated spherulous cells. The main mechanisms of A. cavernicola regeneration are cell dedifferentiation with active migration and subsequent redifferentiation or transdifferentiation of polypotent cells through the mesenchymal‐to‐epithelial transformation. The main cell sources of the regeneration are archaeocytes and choanocytes. At early stages of the regeneration, the blastema almost devoid of cell proliferation, but after 24 hr postoperation (hpo) and up to 72 hpo numerous DNA‐synthesizing cells appear there. In contrast to intact tissues, where vast majority of DNA‐synthesizing cells are choanocytes, all 5‐ethynyl‐2′‐deoxyuridine‐labeled cells in the blastema are mesohyl cells. Intact tissues, distant from the wound, retains intact level of cell proliferation during whole regeneration process. For the first time, the apoptosis was studied during the regeneration of sponges. Two waves of apoptosis were detected during A. cavernicola regeneration: The first wave at 6–12 hpo and the second wave at 48–72 hpo. The epithelialization of the wound in the demosponge Aplysina cavernicola is completed within 2 days, and the wound is completely healed within 2 weeks. The regeneration is accompanied with the formation of a blastema, consisting of archaeocytes, dedifferentiated choanocytes, and other cells. The main mechanisms of regeneration are cell dedifferentiation with subsequent transdifferentiation of cells through the mesenchymal‐to‐epithelial transformation. Research Highlights Regeneration in Aplysina cavernicola is accompanied with the formation of a blastema, cell dedifferentiation and re‐ or transdifferentiation through the mesenchymal‐to‐epithelial transformation. Apoptosis participate in regeneration.</description><subject>Animals</subject><subject>apoptosis</subject><subject>blastema</subject><subject>Cell Differentiation</subject><subject>Cell Transdifferentiation - physiology</subject><subject>demosponges</subject><subject>Development Biology</subject><subject>Embryology and Organogenesis</subject><subject>Life Sciences</subject><subject>mesenchymal‐to‐epithelial transformation</subject><subject>Morphogenesis</subject><subject>Porifera - cytology</subject><subject>Porifera - physiology</subject><subject>Regeneration</subject><subject>transdifferentiation</subject><issn>1552-5007</issn><issn>1552-5015</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kb9u2zAQh4kgRZ24nboXGmMEdnikqD9j4iRNCwPpkC5dCFI62TQkUiHlFs6UR8gz5kkqW4nHLjzi8N13wP0I-QJ0BpSyizU-zfSMsRzyI3ICQrCpoCCOD3-ajshpCOseTqgQH8mIQ8oE5PEJaR-8sqE0VYUebWdUZ5yNlC2jBgPaYrVtVP36_NK5_sHWdCusjaqjbjdm9nC58cYuI49LtOgHgbHRNTYutM4ujcLo7Kfzpl-hJp_Ih0rVAT-_1TH5dXvzML-bLu6_fZ9fLqZFTHk-TXSVxBlqHjMNVZJQ1GUOaZ7mQucs0UBTYDzLaKZThQVSzpMszSBTSAVoysdkMnhXqpatN43yW-mUkXeXC7nrUcZFzGP4Az17NrCtd48bDJ1sTCiwrpVFtwmScYhFGvNkh54PaOFdCB6rgxuo3MUh-ziklvs4evrrm3ijGywP7Pv9e4ANwF9T4_Z_Lvnj5vfVYP0H19iYKQ</recordid><startdate>202001</startdate><enddate>202001</enddate><creator>Ereskovsky, Alexander V.</creator><creator>Tokina, Daria B.</creator><creator>Saidov, Danial M.</creator><creator>Baghdiguian, Stephen</creator><creator>Le Goff, Emilie</creator><creator>Lavrov, Andrey I.</creator><general>Wiley</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>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0003-1079-7204</orcidid><orcidid>https://orcid.org/0000-0002-2992-9708</orcidid><orcidid>https://orcid.org/0000-0002-0788-9039</orcidid></search><sort><creationdate>202001</creationdate><title>Transdifferentiation and mesenchymal‐to‐epithelial transition during regeneration in Demospongiae (Porifera)</title><author>Ereskovsky, Alexander V. ; Tokina, Daria B. ; Saidov, Danial M. ; Baghdiguian, Stephen ; Le Goff, Emilie ; Lavrov, Andrey I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4039-6bf648eb342b1f660ebd9179795b926b1071238808b7aece033687818ae051b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>apoptosis</topic><topic>blastema</topic><topic>Cell Differentiation</topic><topic>Cell Transdifferentiation - physiology</topic><topic>demosponges</topic><topic>Development Biology</topic><topic>Embryology and Organogenesis</topic><topic>Life Sciences</topic><topic>mesenchymal‐to‐epithelial transformation</topic><topic>Morphogenesis</topic><topic>Porifera - cytology</topic><topic>Porifera - physiology</topic><topic>Regeneration</topic><topic>transdifferentiation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ereskovsky, Alexander V.</creatorcontrib><creatorcontrib>Tokina, Daria B.</creatorcontrib><creatorcontrib>Saidov, Danial M.</creatorcontrib><creatorcontrib>Baghdiguian, Stephen</creatorcontrib><creatorcontrib>Le Goff, Emilie</creatorcontrib><creatorcontrib>Lavrov, Andrey I.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Journal of experimental zoology. Part B, Molecular and developmental evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ereskovsky, Alexander V.</au><au>Tokina, Daria B.</au><au>Saidov, Danial M.</au><au>Baghdiguian, Stephen</au><au>Le Goff, Emilie</au><au>Lavrov, Andrey I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transdifferentiation and mesenchymal‐to‐epithelial transition during regeneration in Demospongiae (Porifera)</atitle><jtitle>Journal of experimental zoology. Part B, Molecular and developmental evolution</jtitle><addtitle>J Exp Zool B Mol Dev Evol</addtitle><date>2020-01</date><risdate>2020</risdate><volume>334</volume><issue>1</issue><spage>37</spage><epage>58</epage><pages>37-58</pages><issn>1552-5007</issn><eissn>1552-5015</eissn><abstract>Origin and early evolution of regeneration mechanisms remain among the most pressing questions in animal regeneration biology. Porifera have exceptional regenerative capacities and, as early Metazoan lineage, are a promising model for studying evolutionary aspects of regeneration. Here, we focus on reparative regeneration of the body wall in the Mediterranean demosponge Aplysina cavernicola. The epithelialization of the wound surface is completed within 2 days, and the wound is completely healed within 2 weeks. The regeneration is accompanied with the formation of a mass of undifferentiated cells (blastema), which consists of archaeocytes, dedifferentiated choanocytes, anucleated amoebocytes, and differentiated spherulous cells. The main mechanisms of A. cavernicola regeneration are cell dedifferentiation with active migration and subsequent redifferentiation or transdifferentiation of polypotent cells through the mesenchymal‐to‐epithelial transformation. The main cell sources of the regeneration are archaeocytes and choanocytes. At early stages of the regeneration, the blastema almost devoid of cell proliferation, but after 24 hr postoperation (hpo) and up to 72 hpo numerous DNA‐synthesizing cells appear there. In contrast to intact tissues, where vast majority of DNA‐synthesizing cells are choanocytes, all 5‐ethynyl‐2′‐deoxyuridine‐labeled cells in the blastema are mesohyl cells. Intact tissues, distant from the wound, retains intact level of cell proliferation during whole regeneration process. For the first time, the apoptosis was studied during the regeneration of sponges. Two waves of apoptosis were detected during A. cavernicola regeneration: The first wave at 6–12 hpo and the second wave at 48–72 hpo. The epithelialization of the wound in the demosponge Aplysina cavernicola is completed within 2 days, and the wound is completely healed within 2 weeks. The regeneration is accompanied with the formation of a blastema, consisting of archaeocytes, dedifferentiated choanocytes, and other cells. The main mechanisms of regeneration are cell dedifferentiation with subsequent transdifferentiation of cells through the mesenchymal‐to‐epithelial transformation. Research Highlights Regeneration in Aplysina cavernicola is accompanied with the formation of a blastema, cell dedifferentiation and re‐ or transdifferentiation through the mesenchymal‐to‐epithelial transformation. Apoptosis participate in regeneration.</abstract><cop>United States</cop><pub>Wiley</pub><pmid>31725194</pmid><doi>10.1002/jez.b.22919</doi><tpages>22</tpages><orcidid>https://orcid.org/0000-0003-1079-7204</orcidid><orcidid>https://orcid.org/0000-0002-2992-9708</orcidid><orcidid>https://orcid.org/0000-0002-0788-9039</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1552-5007
ispartof Journal of experimental zoology. Part B, Molecular and developmental evolution, 2020-01, Vol.334 (1), p.37-58
issn 1552-5007
1552-5015
language eng
recordid cdi_hal_primary_oai_HAL_hal_02354341v1
source MEDLINE; Access via Wiley Online Library
subjects Animals
apoptosis
blastema
Cell Differentiation
Cell Transdifferentiation - physiology
demosponges
Development Biology
Embryology and Organogenesis
Life Sciences
mesenchymal‐to‐epithelial transformation
Morphogenesis
Porifera - cytology
Porifera - physiology
Regeneration
transdifferentiation
title Transdifferentiation and mesenchymal‐to‐epithelial transition during regeneration in Demospongiae (Porifera)
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T19%3A40%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Transdifferentiation%20and%20mesenchymal%E2%80%90to%E2%80%90epithelial%20transition%20during%20regeneration%20in%20Demospongiae%20(Porifera)&rft.jtitle=Journal%20of%20experimental%20zoology.%20Part%20B,%20Molecular%20and%20developmental%20evolution&rft.au=Ereskovsky,%20Alexander%20V.&rft.date=2020-01&rft.volume=334&rft.issue=1&rft.spage=37&rft.epage=58&rft.pages=37-58&rft.issn=1552-5007&rft.eissn=1552-5015&rft_id=info:doi/10.1002/jez.b.22919&rft_dat=%3Cproquest_hal_p%3E2314574361%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2314574361&rft_id=info:pmid/31725194&rfr_iscdi=true