Intermediate filament typing of the human embryonic and fetal notochord
In order to characterize human notochordal tissue we investigated notochords from 32 human embryos and fetuses ranging between the 5th and 13th gestational week, using immunohistochemistry to detect intermediate filament proteins cytokeratin, vimentin and desmin, the cytokeratin subtypes 7, 8, 18, 1...
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Veröffentlicht in: | Cell and tissue research 1995-05, Vol.280 (2), p.455-462 |
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creator | Götz, W Kasper, M Fischer, G Herken, R |
description | In order to characterize human notochordal tissue we investigated notochords from 32 human embryos and fetuses ranging between the 5th and 13th gestational week, using immunohistochemistry to detect intermediate filament proteins cytokeratin, vimentin and desmin, the cytokeratin subtypes 7, 8, 18, 19 and 20, epithelial membrane antigen (EMA), and adhesion molecules pan-cadherin and E-cadherin. Strong immunoreactions could be demonstrated for pan-cytokeratin, but not for desmin or EMA. Staining for pan-cadherin and weak staining for E-cadherin was found on cell membranes of notochordal cells. Also it was demonstrated that notochordal cells of all developmental stages contain the cytokeratins 8, 18 and 19, but not 7 or 20. Some cells in the embryonic notochord also contained some vimentin. Vimentin reactivity increased between the 8th and 13th gestational week parallel to morphological changes leading from an epithelial phenotype to the chorda reticulum which represents a mesenchymal tissue within the intervertebral disc anlagen. This coexpression reflects the epithelial-mesenchymal transformation of the notochord, which also loses E-cadherin expression during later stages. Our findings cannot elucidate a histogenetic germ layer origin of the human notochord but demonstrate its epithelial character. Thus, morphogenetic inductive processes between the human notochord and its surrounding vertebral column anlagen can be classified as epithelial-mesenchymal interactions. |
doi_str_mv | 10.1007/BF00307819 |
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Strong immunoreactions could be demonstrated for pan-cytokeratin, but not for desmin or EMA. Staining for pan-cadherin and weak staining for E-cadherin was found on cell membranes of notochordal cells. Also it was demonstrated that notochordal cells of all developmental stages contain the cytokeratins 8, 18 and 19, but not 7 or 20. Some cells in the embryonic notochord also contained some vimentin. Vimentin reactivity increased between the 8th and 13th gestational week parallel to morphological changes leading from an epithelial phenotype to the chorda reticulum which represents a mesenchymal tissue within the intervertebral disc anlagen. This coexpression reflects the epithelial-mesenchymal transformation of the notochord, which also loses E-cadherin expression during later stages. Our findings cannot elucidate a histogenetic germ layer origin of the human notochord but demonstrate its epithelial character. Thus, morphogenetic inductive processes between the human notochord and its surrounding vertebral column anlagen can be classified as epithelial-mesenchymal interactions.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/BF00307819</identifier><identifier>PMID: 7781042</identifier><language>eng</language><publisher>Germany</publisher><subject>Antibodies, Monoclonal - immunology ; Fetal Proteins - analysis ; Gestational Age ; Humans ; Intermediate Filament Proteins - analysis ; Intermediate Filament Proteins - immunology ; Intermediate Filaments - chemistry ; Morphogenesis ; Notochord - chemistry ; Notochord - cytology ; Notochord - ultrastructure</subject><ispartof>Cell and tissue research, 1995-05, Vol.280 (2), p.455-462</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c282t-422164e1795d4441236f13589f05a6678a70839497fe246e704a01d4bce344d3</citedby><cites>FETCH-LOGICAL-c282t-422164e1795d4441236f13589f05a6678a70839497fe246e704a01d4bce344d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7781042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Götz, W</creatorcontrib><creatorcontrib>Kasper, M</creatorcontrib><creatorcontrib>Fischer, G</creatorcontrib><creatorcontrib>Herken, R</creatorcontrib><title>Intermediate filament typing of the human embryonic and fetal notochord</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><description>In order to characterize human notochordal tissue we investigated notochords from 32 human embryos and fetuses ranging between the 5th and 13th gestational week, using immunohistochemistry to detect intermediate filament proteins cytokeratin, vimentin and desmin, the cytokeratin subtypes 7, 8, 18, 19 and 20, epithelial membrane antigen (EMA), and adhesion molecules pan-cadherin and E-cadherin. Strong immunoreactions could be demonstrated for pan-cytokeratin, but not for desmin or EMA. Staining for pan-cadherin and weak staining for E-cadherin was found on cell membranes of notochordal cells. Also it was demonstrated that notochordal cells of all developmental stages contain the cytokeratins 8, 18 and 19, but not 7 or 20. Some cells in the embryonic notochord also contained some vimentin. Vimentin reactivity increased between the 8th and 13th gestational week parallel to morphological changes leading from an epithelial phenotype to the chorda reticulum which represents a mesenchymal tissue within the intervertebral disc anlagen. This coexpression reflects the epithelial-mesenchymal transformation of the notochord, which also loses E-cadherin expression during later stages. Our findings cannot elucidate a histogenetic germ layer origin of the human notochord but demonstrate its epithelial character. Thus, morphogenetic inductive processes between the human notochord and its surrounding vertebral column anlagen can be classified as epithelial-mesenchymal interactions.</description><subject>Antibodies, Monoclonal - immunology</subject><subject>Fetal Proteins - analysis</subject><subject>Gestational Age</subject><subject>Humans</subject><subject>Intermediate Filament Proteins - analysis</subject><subject>Intermediate Filament Proteins - immunology</subject><subject>Intermediate Filaments - chemistry</subject><subject>Morphogenesis</subject><subject>Notochord - chemistry</subject><subject>Notochord - cytology</subject><subject>Notochord - ultrastructure</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0D9PwzAQhnELgUopLOxInhiQAuc_tZMRKloqVWLpwBY5yZkGJXaxnaHfnqBWMJ10-ukdHkJuGTwyAP30sgQQoHNWnJEpk4JnkOv8nEzHL8-0Uh-X5CrGLwAmlSomZKJHDJJPyWrtEoYem9YkpLbtTI8u0XTYt-6TekvTDulu6I2j2Ffh4F1bU-MaajGZjjqffL3zobkmF9Z0EW9Od0a2y9ft4i3bvK_Wi-dNVvOcp0xyzpREpot5I6VkXCjLxDwvLMyNUjo3GnJRyEJb5FKhBmmANbKqUUjZiBm5P87ug_8eMKayb2ONXWcc-iGWWgvBtIQRPhxhHXyMAW25D21vwqFkUP5GK_-jjfjutDpUY4o_eqokfgA-OmUJ</recordid><startdate>199505</startdate><enddate>199505</enddate><creator>Götz, W</creator><creator>Kasper, M</creator><creator>Fischer, G</creator><creator>Herken, R</creator><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></search><sort><creationdate>199505</creationdate><title>Intermediate filament typing of the human embryonic and fetal notochord</title><author>Götz, W ; Kasper, M ; Fischer, G ; Herken, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-422164e1795d4441236f13589f05a6678a70839497fe246e704a01d4bce344d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Antibodies, Monoclonal - immunology</topic><topic>Fetal Proteins - analysis</topic><topic>Gestational Age</topic><topic>Humans</topic><topic>Intermediate Filament Proteins - analysis</topic><topic>Intermediate Filament Proteins - immunology</topic><topic>Intermediate Filaments - chemistry</topic><topic>Morphogenesis</topic><topic>Notochord - chemistry</topic><topic>Notochord - cytology</topic><topic>Notochord - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Götz, W</creatorcontrib><creatorcontrib>Kasper, M</creatorcontrib><creatorcontrib>Fischer, G</creatorcontrib><creatorcontrib>Herken, R</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><jtitle>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Götz, W</au><au>Kasper, M</au><au>Fischer, G</au><au>Herken, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intermediate filament typing of the human embryonic and fetal notochord</atitle><jtitle>Cell and tissue research</jtitle><addtitle>Cell Tissue Res</addtitle><date>1995-05</date><risdate>1995</risdate><volume>280</volume><issue>2</issue><spage>455</spage><epage>462</epage><pages>455-462</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><abstract>In order to characterize human notochordal tissue we investigated notochords from 32 human embryos and fetuses ranging between the 5th and 13th gestational week, using immunohistochemistry to detect intermediate filament proteins cytokeratin, vimentin and desmin, the cytokeratin subtypes 7, 8, 18, 19 and 20, epithelial membrane antigen (EMA), and adhesion molecules pan-cadherin and E-cadherin. Strong immunoreactions could be demonstrated for pan-cytokeratin, but not for desmin or EMA. Staining for pan-cadherin and weak staining for E-cadherin was found on cell membranes of notochordal cells. Also it was demonstrated that notochordal cells of all developmental stages contain the cytokeratins 8, 18 and 19, but not 7 or 20. Some cells in the embryonic notochord also contained some vimentin. Vimentin reactivity increased between the 8th and 13th gestational week parallel to morphological changes leading from an epithelial phenotype to the chorda reticulum which represents a mesenchymal tissue within the intervertebral disc anlagen. This coexpression reflects the epithelial-mesenchymal transformation of the notochord, which also loses E-cadherin expression during later stages. Our findings cannot elucidate a histogenetic germ layer origin of the human notochord but demonstrate its epithelial character. Thus, morphogenetic inductive processes between the human notochord and its surrounding vertebral column anlagen can be classified as epithelial-mesenchymal interactions.</abstract><cop>Germany</cop><pmid>7781042</pmid><doi>10.1007/BF00307819</doi><tpages>8</tpages></addata></record> |
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subjects | Antibodies, Monoclonal - immunology Fetal Proteins - analysis Gestational Age Humans Intermediate Filament Proteins - analysis Intermediate Filament Proteins - immunology Intermediate Filaments - chemistry Morphogenesis Notochord - chemistry Notochord - cytology Notochord - ultrastructure |
title | Intermediate filament typing of the human embryonic and fetal notochord |
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