Cellular composition and organization of the spinal cord central canal during metamorphosis of the frog Xenopus laevis
Studying the cellular composition and morphological changes of cells lining the central canal during Xenopus laevis metamorphosis could contribute to understand postnatal development and spinal cord regeneration. Here we report the analysis of central canal cells at different stages during metamorph...
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Veröffentlicht in: | Journal of comparative neurology (1911) 2018-07, Vol.526 (10), p.1712-1732 |
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container_title | Journal of comparative neurology (1911) |
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creator | Edwards‐Faret, Gabriela Cebrián‐Silla, Arantxa Méndez‐Olivos, Emilio E. González‐Pinto, Karina García‐Verdugo, José Manuel Larraín, Juan |
description | Studying the cellular composition and morphological changes of cells lining the central canal during Xenopus laevis metamorphosis could contribute to understand postnatal development and spinal cord regeneration. Here we report the analysis of central canal cells at different stages during metamorphosis using immunofluorescence for protein markers expression, transmission and scanning electron microscopy and cell proliferation assays. The central canal was regionalized according to expression of glial markers, ultrastructure, and proliferation in dorsal, lateral, and ventral domains with differences between larvae and froglets. In regenerative larvae, all cell types were uniciliated, have a radial morphology, and elongated nuclei with lax chromatin, resembling radial glial cells. Important differences in cells of nonregenerative froglets were observed, although uniciliated cells were found, the most abundant cells had multicilia and revealed extensive changes in the maturation and differentiation state. The majority of dividing cells in larvae corresponded to uniciliated cells at dorsal and lateral domains in a cervical‐lumbar gradient, correlating with undifferentiated features. Neurons contacting the lumen of the central canal were detected in both stages and revealed extensive changes in the maturation and differentiation state. However, in froglets a very low proportion of cells incorporate 5‐ethynyl‐2′‐deoxyuridine (EdU), associated with the differentiated profile and with the increase of multiciliated cells. Our work showed progressive changes in the cell types lining the central canal of Xenopus laevis spinal cord which are correlated with the regenerative capacities.
Using immunofluorescence for protein markers, transmission and scanning electron microscopy and cell proliferation assays, the authors show progressive changes in the cell types lining the central canal spinal cord in Xenopus laevis. These cells types are correlated with the regenerative capacities and its progressive decrease during metamorphosis. |
doi_str_mv | 10.1002/cne.24441 |
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Using immunofluorescence for protein markers, transmission and scanning electron microscopy and cell proliferation assays, the authors show progressive changes in the cell types lining the central canal spinal cord in Xenopus laevis. These cells types are correlated with the regenerative capacities and its progressive decrease during metamorphosis.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.24441</identifier><identifier>PMID: 29603210</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Cell proliferation ; central canal ; Chromatin ; Cytology ; ependymal cells ; Glial cells ; Immunofluorescence ; Larvae ; Metamorphosis ; Radial glial cells ; Regeneration ; RRID:AB_10000325 ; RRID:AB_10560516 ; RRID:AB_10693771 ; RRID:AB_2110656 ; RRID:AB_2315078 ; RRID:AB_261795 ; RRID:AB_476857 ; RRID:AB_477499 ; RRID:AB_528507 ; Scanning electron microscopy ; Spinal cord ; Ultrastructure ; Xenopus laevis</subject><ispartof>Journal of comparative neurology (1911), 2018-07, Vol.526 (10), p.1712-1732</ispartof><rights>2018 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3531-781393dc68391ba5bf15aa22289360a3bdba3a307d62aa649a722fb875ac047c3</citedby><cites>FETCH-LOGICAL-c3531-781393dc68391ba5bf15aa22289360a3bdba3a307d62aa649a722fb875ac047c3</cites><orcidid>0000-0003-0598-9682</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%2Fcne.24441$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcne.24441$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29603210$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Edwards‐Faret, Gabriela</creatorcontrib><creatorcontrib>Cebrián‐Silla, Arantxa</creatorcontrib><creatorcontrib>Méndez‐Olivos, Emilio E.</creatorcontrib><creatorcontrib>González‐Pinto, Karina</creatorcontrib><creatorcontrib>García‐Verdugo, José Manuel</creatorcontrib><creatorcontrib>Larraín, Juan</creatorcontrib><title>Cellular composition and organization of the spinal cord central canal during metamorphosis of the frog Xenopus laevis</title><title>Journal of comparative neurology (1911)</title><addtitle>J Comp Neurol</addtitle><description>Studying the cellular composition and morphological changes of cells lining the central canal during Xenopus laevis metamorphosis could contribute to understand postnatal development and spinal cord regeneration. Here we report the analysis of central canal cells at different stages during metamorphosis using immunofluorescence for protein markers expression, transmission and scanning electron microscopy and cell proliferation assays. The central canal was regionalized according to expression of glial markers, ultrastructure, and proliferation in dorsal, lateral, and ventral domains with differences between larvae and froglets. In regenerative larvae, all cell types were uniciliated, have a radial morphology, and elongated nuclei with lax chromatin, resembling radial glial cells. Important differences in cells of nonregenerative froglets were observed, although uniciliated cells were found, the most abundant cells had multicilia and revealed extensive changes in the maturation and differentiation state. The majority of dividing cells in larvae corresponded to uniciliated cells at dorsal and lateral domains in a cervical‐lumbar gradient, correlating with undifferentiated features. Neurons contacting the lumen of the central canal were detected in both stages and revealed extensive changes in the maturation and differentiation state. However, in froglets a very low proportion of cells incorporate 5‐ethynyl‐2′‐deoxyuridine (EdU), associated with the differentiated profile and with the increase of multiciliated cells. Our work showed progressive changes in the cell types lining the central canal of Xenopus laevis spinal cord which are correlated with the regenerative capacities.
Using immunofluorescence for protein markers, transmission and scanning electron microscopy and cell proliferation assays, the authors show progressive changes in the cell types lining the central canal spinal cord in Xenopus laevis. These cells types are correlated with the regenerative capacities and its progressive decrease during metamorphosis.</description><subject>Cell proliferation</subject><subject>central canal</subject><subject>Chromatin</subject><subject>Cytology</subject><subject>ependymal cells</subject><subject>Glial cells</subject><subject>Immunofluorescence</subject><subject>Larvae</subject><subject>Metamorphosis</subject><subject>Radial glial cells</subject><subject>Regeneration</subject><subject>RRID:AB_10000325</subject><subject>RRID:AB_10560516</subject><subject>RRID:AB_10693771</subject><subject>RRID:AB_2110656</subject><subject>RRID:AB_2315078</subject><subject>RRID:AB_261795</subject><subject>RRID:AB_476857</subject><subject>RRID:AB_477499</subject><subject>RRID:AB_528507</subject><subject>Scanning electron microscopy</subject><subject>Spinal cord</subject><subject>Ultrastructure</subject><subject>Xenopus laevis</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kcFO3DAQhi1UBFvKgReoLPVCD4GxnTjxsVpBW2kFF5B6iyaOs2uU2KmdgLZPXy_L9lCJkzUznz9p5ifkgsEVA-DX2pkrnuc5OyILBkpmqpLsA1mkGcuUkuUp-RjjEwAoJaoTcsqVBMEZLMjz0vT93GOg2g-jj3ay3lF0LfVhjc7-wdeG7-i0MTSO1mGf0NBSbdwUdgXuWu0crFvTwUw4-DBukikefnXBr-kv4_w4R9qjebbxEznusI_m_O09I4-3Nw_LH9nq_vvP5bdVpkUhWFZWTCjRalkJxRosmo4ViJzzSgkJKJq2QYECylZyRJkrLDnvmqosUENeanFGLvfeMfjfs4lTPdio08rojJ9jzYFDrkCKKqFf_kOf_BzSbjtKVEwWUKhEfd1TOvgYg-nqMdgBw7ZmUO_CqFMY9WsYif38ZpybwbT_yMP1E3C9B15sb7bvm-rl3c1e-RfFJZPZ</recordid><startdate>20180701</startdate><enddate>20180701</enddate><creator>Edwards‐Faret, Gabriela</creator><creator>Cebrián‐Silla, Arantxa</creator><creator>Méndez‐Olivos, Emilio E.</creator><creator>González‐Pinto, Karina</creator><creator>García‐Verdugo, José Manuel</creator><creator>Larraín, Juan</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0598-9682</orcidid></search><sort><creationdate>20180701</creationdate><title>Cellular composition and organization of the spinal cord central canal during metamorphosis of the frog Xenopus laevis</title><author>Edwards‐Faret, Gabriela ; Cebrián‐Silla, Arantxa ; Méndez‐Olivos, Emilio E. ; González‐Pinto, Karina ; García‐Verdugo, José Manuel ; Larraín, Juan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3531-781393dc68391ba5bf15aa22289360a3bdba3a307d62aa649a722fb875ac047c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Cell proliferation</topic><topic>central canal</topic><topic>Chromatin</topic><topic>Cytology</topic><topic>ependymal cells</topic><topic>Glial cells</topic><topic>Immunofluorescence</topic><topic>Larvae</topic><topic>Metamorphosis</topic><topic>Radial glial cells</topic><topic>Regeneration</topic><topic>RRID:AB_10000325</topic><topic>RRID:AB_10560516</topic><topic>RRID:AB_10693771</topic><topic>RRID:AB_2110656</topic><topic>RRID:AB_2315078</topic><topic>RRID:AB_261795</topic><topic>RRID:AB_476857</topic><topic>RRID:AB_477499</topic><topic>RRID:AB_528507</topic><topic>Scanning electron microscopy</topic><topic>Spinal cord</topic><topic>Ultrastructure</topic><topic>Xenopus laevis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Edwards‐Faret, Gabriela</creatorcontrib><creatorcontrib>Cebrián‐Silla, Arantxa</creatorcontrib><creatorcontrib>Méndez‐Olivos, Emilio E.</creatorcontrib><creatorcontrib>González‐Pinto, Karina</creatorcontrib><creatorcontrib>García‐Verdugo, José Manuel</creatorcontrib><creatorcontrib>Larraín, Juan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Edwards‐Faret, Gabriela</au><au>Cebrián‐Silla, Arantxa</au><au>Méndez‐Olivos, Emilio E.</au><au>González‐Pinto, Karina</au><au>García‐Verdugo, José Manuel</au><au>Larraín, Juan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular composition and organization of the spinal cord central canal during metamorphosis of the frog Xenopus laevis</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J Comp Neurol</addtitle><date>2018-07-01</date><risdate>2018</risdate><volume>526</volume><issue>10</issue><spage>1712</spage><epage>1732</epage><pages>1712-1732</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Studying the cellular composition and morphological changes of cells lining the central canal during Xenopus laevis metamorphosis could contribute to understand postnatal development and spinal cord regeneration. Here we report the analysis of central canal cells at different stages during metamorphosis using immunofluorescence for protein markers expression, transmission and scanning electron microscopy and cell proliferation assays. The central canal was regionalized according to expression of glial markers, ultrastructure, and proliferation in dorsal, lateral, and ventral domains with differences between larvae and froglets. In regenerative larvae, all cell types were uniciliated, have a radial morphology, and elongated nuclei with lax chromatin, resembling radial glial cells. Important differences in cells of nonregenerative froglets were observed, although uniciliated cells were found, the most abundant cells had multicilia and revealed extensive changes in the maturation and differentiation state. The majority of dividing cells in larvae corresponded to uniciliated cells at dorsal and lateral domains in a cervical‐lumbar gradient, correlating with undifferentiated features. Neurons contacting the lumen of the central canal were detected in both stages and revealed extensive changes in the maturation and differentiation state. However, in froglets a very low proportion of cells incorporate 5‐ethynyl‐2′‐deoxyuridine (EdU), associated with the differentiated profile and with the increase of multiciliated cells. Our work showed progressive changes in the cell types lining the central canal of Xenopus laevis spinal cord which are correlated with the regenerative capacities.
Using immunofluorescence for protein markers, transmission and scanning electron microscopy and cell proliferation assays, the authors show progressive changes in the cell types lining the central canal spinal cord in Xenopus laevis. These cells types are correlated with the regenerative capacities and its progressive decrease during metamorphosis.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29603210</pmid><doi>10.1002/cne.24441</doi><tpages>22</tpages><orcidid>https://orcid.org/0000-0003-0598-9682</orcidid></addata></record> |
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subjects | Cell proliferation central canal Chromatin Cytology ependymal cells Glial cells Immunofluorescence Larvae Metamorphosis Radial glial cells Regeneration RRID:AB_10000325 RRID:AB_10560516 RRID:AB_10693771 RRID:AB_2110656 RRID:AB_2315078 RRID:AB_261795 RRID:AB_476857 RRID:AB_477499 RRID:AB_528507 Scanning electron microscopy Spinal cord Ultrastructure Xenopus laevis |
title | Cellular composition and organization of the spinal cord central canal during metamorphosis of the frog Xenopus laevis |
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