Histochemical localization of skin glycosaminoglycans during feather development in the chick embryo

The distribution of glycosaminoglycans (GAGs) was studied in embryonic chick skin, using alcian blue staining with critical electrolyte concentration and glycanase treatment, immunofluorescence and transmission electron microscopy. Light microscopy revealed an uneven distribution of sulphated and no...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Roux's Archives of Developmental Biology 1987-07, Vol.196 (5), p.303-315
Hauptverfasser: JAHODA, C. A. B, MAUGER, A, SENGEL, P
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 315
container_issue 5
container_start_page 303
container_title Roux's Archives of Developmental Biology
container_volume 196
creator JAHODA, C. A. B
MAUGER, A
SENGEL, P
description The distribution of glycosaminoglycans (GAGs) was studied in embryonic chick skin, using alcian blue staining with critical electrolyte concentration and glycanase treatment, immunofluorescence and transmission electron microscopy. Light microscopy revealed an uneven distribution of sulphated and non-sulphated GAGs at all stages of feather development. Along the dermal-epidermal junction and throughout the depth of the dermis, staining was stronger inside the feathers than in the interplumar skin. With increasing MgCl concentration, the decrease in stain intensity along the dermal-epidermal junction was stronger in interplumar skin than inside feather structures, indicating that sulphated GAGs are more abundant within feathers than in interplumar skin. The same differential sensitivity to electrolyte concentration was noted in the dermis, except at the feather placode stage, when labelling inside the dermal condensation was virtually wiped out at 0.6 M MgCl and higher concentrations, whereas it persisted in the surrounding dermis up to 0.8 M MgCl , indicating that the dermal condensation contains a larger amount of hyaluronate than non-feather-forming dermis. Enzyme treatment of sections with Streptomyces hyaluronidase as compared with those treated with chondroitinase ABC corroborated these findings. Immunofluorescent detection of heparan sulphate proteoglycan revealed the presence of the antigen along the dermal-epidermal junction at all stages of feather development, with peaks of brightness in discrete spots of feather structures. Electron microscopy revealed the presence of ruthenium red and tannic acid positive material in the dermal-epidermal junctional zone and inside the dermis. The density of marked granules was somewhat higher in intraplumar than in interplumar regions. These observations demonstrate that certain sulphated and non-sulphated GAGs are distributed in a microheterogeneous manner, which appears to be related to the morphogenetic events of feather development. They are discussed in view of the possible role these components might play in dermal-epidermal interactions. They strengthen the notion, already gained from previous studies on the localization of interstitial collagens and fibronectin, that extracellular matrix components play an important structural and informative role in organogenesis.
doi_str_mv 10.1007/BF00395954
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1007_BF00395954</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1878821616</sourcerecordid><originalsourceid>FETCH-LOGICAL-c314t-d6deebdae6a8dd04ea83e0cc04fa0c9ada42ebc316698681aca37f0c13a3c7803</originalsourceid><addsrcrecordid>eNpF0E1PwzAMBuAIgWB8XPgBKAcOCKngNGmbHmFigITEBSRulZe4W1jbjKRDGr-eIsa42Jb12IeXsVMBVwKguL6dAMgyKzO1w0ZCyTQBJd522QhKCQnI7O2AHcb4DpBDkap9dpBqCVmWpSNmH1zsvZlT6ww2vPFDdV_YO99xX_O4cB2fNWvjI7au8z8jdpHbVXDdjNeE_ZwCt_RJjV-21PV8OBh23MydWXBqp2Htj9lejU2kk00_Yq-Tu5fxQ_L0fP84vnlKjBSqT2xuiaYWKUdtLShCLQmMAVUjmBItqpSmg83zUudaoEFZ1GCERGkKDfKIXfz-XQb_saLYV62LhpoGO_KrWAldaJ2KXOQDvfylJvgYA9XVMrgWw7oSUP2kWv2nOuCzzd_VtCW7pX8xDuB8AzAOAdYBO-Pi1mkpdKmE_AZ-3YFl</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1878821616</pqid></control><display><type>article</type><title>Histochemical localization of skin glycosaminoglycans during feather development in the chick embryo</title><source>Springer Nature - Complete Springer Journals</source><creator>JAHODA, C. A. B ; MAUGER, A ; SENGEL, P</creator><creatorcontrib>JAHODA, C. A. B ; MAUGER, A ; SENGEL, P</creatorcontrib><description>The distribution of glycosaminoglycans (GAGs) was studied in embryonic chick skin, using alcian blue staining with critical electrolyte concentration and glycanase treatment, immunofluorescence and transmission electron microscopy. Light microscopy revealed an uneven distribution of sulphated and non-sulphated GAGs at all stages of feather development. Along the dermal-epidermal junction and throughout the depth of the dermis, staining was stronger inside the feathers than in the interplumar skin. With increasing MgCl concentration, the decrease in stain intensity along the dermal-epidermal junction was stronger in interplumar skin than inside feather structures, indicating that sulphated GAGs are more abundant within feathers than in interplumar skin. The same differential sensitivity to electrolyte concentration was noted in the dermis, except at the feather placode stage, when labelling inside the dermal condensation was virtually wiped out at 0.6 M MgCl and higher concentrations, whereas it persisted in the surrounding dermis up to 0.8 M MgCl , indicating that the dermal condensation contains a larger amount of hyaluronate than non-feather-forming dermis. Enzyme treatment of sections with Streptomyces hyaluronidase as compared with those treated with chondroitinase ABC corroborated these findings. Immunofluorescent detection of heparan sulphate proteoglycan revealed the presence of the antigen along the dermal-epidermal junction at all stages of feather development, with peaks of brightness in discrete spots of feather structures. Electron microscopy revealed the presence of ruthenium red and tannic acid positive material in the dermal-epidermal junctional zone and inside the dermis. The density of marked granules was somewhat higher in intraplumar than in interplumar regions. These observations demonstrate that certain sulphated and non-sulphated GAGs are distributed in a microheterogeneous manner, which appears to be related to the morphogenetic events of feather development. They are discussed in view of the possible role these components might play in dermal-epidermal interactions. They strengthen the notion, already gained from previous studies on the localization of interstitial collagens and fibronectin, that extracellular matrix components play an important structural and informative role in organogenesis.</description><identifier>ISSN: 0930-035X</identifier><identifier>EISSN: 1432-041X</identifier><identifier>DOI: 10.1007/BF00395954</identifier><identifier>PMID: 28305552</identifier><identifier>CODEN: WRABDT</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Biological and medical sciences ; Embryology: invertebrates and vertebrates. Teratology ; Fundamental and applied biological sciences. Psychology ; Organogenesis. Fetal development ; Organogenesis. Physiological fonctions</subject><ispartof>Roux's Archives of Developmental Biology, 1987-07, Vol.196 (5), p.303-315</ispartof><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c314t-d6deebdae6a8dd04ea83e0cc04fa0c9ada42ebc316698681aca37f0c13a3c7803</citedby><cites>FETCH-LOGICAL-c314t-d6deebdae6a8dd04ea83e0cc04fa0c9ada42ebc316698681aca37f0c13a3c7803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=8318941$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28305552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>JAHODA, C. A. B</creatorcontrib><creatorcontrib>MAUGER, A</creatorcontrib><creatorcontrib>SENGEL, P</creatorcontrib><title>Histochemical localization of skin glycosaminoglycans during feather development in the chick embryo</title><title>Roux's Archives of Developmental Biology</title><addtitle>Roux Arch Dev Biol</addtitle><description>The distribution of glycosaminoglycans (GAGs) was studied in embryonic chick skin, using alcian blue staining with critical electrolyte concentration and glycanase treatment, immunofluorescence and transmission electron microscopy. Light microscopy revealed an uneven distribution of sulphated and non-sulphated GAGs at all stages of feather development. Along the dermal-epidermal junction and throughout the depth of the dermis, staining was stronger inside the feathers than in the interplumar skin. With increasing MgCl concentration, the decrease in stain intensity along the dermal-epidermal junction was stronger in interplumar skin than inside feather structures, indicating that sulphated GAGs are more abundant within feathers than in interplumar skin. The same differential sensitivity to electrolyte concentration was noted in the dermis, except at the feather placode stage, when labelling inside the dermal condensation was virtually wiped out at 0.6 M MgCl and higher concentrations, whereas it persisted in the surrounding dermis up to 0.8 M MgCl , indicating that the dermal condensation contains a larger amount of hyaluronate than non-feather-forming dermis. Enzyme treatment of sections with Streptomyces hyaluronidase as compared with those treated with chondroitinase ABC corroborated these findings. Immunofluorescent detection of heparan sulphate proteoglycan revealed the presence of the antigen along the dermal-epidermal junction at all stages of feather development, with peaks of brightness in discrete spots of feather structures. Electron microscopy revealed the presence of ruthenium red and tannic acid positive material in the dermal-epidermal junctional zone and inside the dermis. The density of marked granules was somewhat higher in intraplumar than in interplumar regions. These observations demonstrate that certain sulphated and non-sulphated GAGs are distributed in a microheterogeneous manner, which appears to be related to the morphogenetic events of feather development. They are discussed in view of the possible role these components might play in dermal-epidermal interactions. They strengthen the notion, already gained from previous studies on the localization of interstitial collagens and fibronectin, that extracellular matrix components play an important structural and informative role in organogenesis.</description><subject>Biological and medical sciences</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Organogenesis. Fetal development</subject><subject>Organogenesis. Physiological fonctions</subject><issn>0930-035X</issn><issn>1432-041X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNpF0E1PwzAMBuAIgWB8XPgBKAcOCKngNGmbHmFigITEBSRulZe4W1jbjKRDGr-eIsa42Jb12IeXsVMBVwKguL6dAMgyKzO1w0ZCyTQBJd522QhKCQnI7O2AHcb4DpBDkap9dpBqCVmWpSNmH1zsvZlT6ww2vPFDdV_YO99xX_O4cB2fNWvjI7au8z8jdpHbVXDdjNeE_ZwCt_RJjV-21PV8OBh23MydWXBqp2Htj9lejU2kk00_Yq-Tu5fxQ_L0fP84vnlKjBSqT2xuiaYWKUdtLShCLQmMAVUjmBItqpSmg83zUudaoEFZ1GCERGkKDfKIXfz-XQb_saLYV62LhpoGO_KrWAldaJ2KXOQDvfylJvgYA9XVMrgWw7oSUP2kWv2nOuCzzd_VtCW7pX8xDuB8AzAOAdYBO-Pi1mkpdKmE_AZ-3YFl</recordid><startdate>198707</startdate><enddate>198707</enddate><creator>JAHODA, C. A. B</creator><creator>MAUGER, A</creator><creator>SENGEL, P</creator><general>Springer</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>198707</creationdate><title>Histochemical localization of skin glycosaminoglycans during feather development in the chick embryo</title><author>JAHODA, C. A. B ; MAUGER, A ; SENGEL, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c314t-d6deebdae6a8dd04ea83e0cc04fa0c9ada42ebc316698681aca37f0c13a3c7803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Biological and medical sciences</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Organogenesis. Fetal development</topic><topic>Organogenesis. Physiological fonctions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>JAHODA, C. A. B</creatorcontrib><creatorcontrib>MAUGER, A</creatorcontrib><creatorcontrib>SENGEL, P</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Roux's Archives of Developmental Biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>JAHODA, C. A. B</au><au>MAUGER, A</au><au>SENGEL, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Histochemical localization of skin glycosaminoglycans during feather development in the chick embryo</atitle><jtitle>Roux's Archives of Developmental Biology</jtitle><addtitle>Roux Arch Dev Biol</addtitle><date>1987-07</date><risdate>1987</risdate><volume>196</volume><issue>5</issue><spage>303</spage><epage>315</epage><pages>303-315</pages><issn>0930-035X</issn><eissn>1432-041X</eissn><coden>WRABDT</coden><abstract>The distribution of glycosaminoglycans (GAGs) was studied in embryonic chick skin, using alcian blue staining with critical electrolyte concentration and glycanase treatment, immunofluorescence and transmission electron microscopy. Light microscopy revealed an uneven distribution of sulphated and non-sulphated GAGs at all stages of feather development. Along the dermal-epidermal junction and throughout the depth of the dermis, staining was stronger inside the feathers than in the interplumar skin. With increasing MgCl concentration, the decrease in stain intensity along the dermal-epidermal junction was stronger in interplumar skin than inside feather structures, indicating that sulphated GAGs are more abundant within feathers than in interplumar skin. The same differential sensitivity to electrolyte concentration was noted in the dermis, except at the feather placode stage, when labelling inside the dermal condensation was virtually wiped out at 0.6 M MgCl and higher concentrations, whereas it persisted in the surrounding dermis up to 0.8 M MgCl , indicating that the dermal condensation contains a larger amount of hyaluronate than non-feather-forming dermis. Enzyme treatment of sections with Streptomyces hyaluronidase as compared with those treated with chondroitinase ABC corroborated these findings. Immunofluorescent detection of heparan sulphate proteoglycan revealed the presence of the antigen along the dermal-epidermal junction at all stages of feather development, with peaks of brightness in discrete spots of feather structures. Electron microscopy revealed the presence of ruthenium red and tannic acid positive material in the dermal-epidermal junctional zone and inside the dermis. The density of marked granules was somewhat higher in intraplumar than in interplumar regions. These observations demonstrate that certain sulphated and non-sulphated GAGs are distributed in a microheterogeneous manner, which appears to be related to the morphogenetic events of feather development. They are discussed in view of the possible role these components might play in dermal-epidermal interactions. They strengthen the notion, already gained from previous studies on the localization of interstitial collagens and fibronectin, that extracellular matrix components play an important structural and informative role in organogenesis.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>28305552</pmid><doi>10.1007/BF00395954</doi><tpages>13</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0930-035X
ispartof Roux's Archives of Developmental Biology, 1987-07, Vol.196 (5), p.303-315
issn 0930-035X
1432-041X
language eng
recordid cdi_crossref_primary_10_1007_BF00395954
source Springer Nature - Complete Springer Journals
subjects Biological and medical sciences
Embryology: invertebrates and vertebrates. Teratology
Fundamental and applied biological sciences. Psychology
Organogenesis. Fetal development
Organogenesis. Physiological fonctions
title Histochemical localization of skin glycosaminoglycans during feather development in the chick embryo
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T23%3A25%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Histochemical%20localization%20of%20skin%20glycosaminoglycans%20during%20feather%20development%20in%20the%20chick%20embryo&rft.jtitle=Roux's%20Archives%20of%20Developmental%20Biology&rft.au=JAHODA,%20C.%20A.%20B&rft.date=1987-07&rft.volume=196&rft.issue=5&rft.spage=303&rft.epage=315&rft.pages=303-315&rft.issn=0930-035X&rft.eissn=1432-041X&rft.coden=WRABDT&rft_id=info:doi/10.1007/BF00395954&rft_dat=%3Cproquest_cross%3E1878821616%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1878821616&rft_id=info:pmid/28305552&rfr_iscdi=true