Molecular size distribution of proteoglycans in human inflamed gingival tissue
Proteoglycans were extracted from human gingiva with 2 M CaCl 2. The extracts were examined by gel filtration on Sephacryl S-400 in 2 M CaCl 2 under dissociative conditions. The 280 nm absorbance profiles of clinically uninflamed, inflamed and severely-inflamed tissues showed that material was prese...
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Veröffentlicht in: | Archives of oral biology 1984, Vol.29 (7), p.513-519 |
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creator | Purvis, J.A. Embery, G. Oliver, W.M. |
description | Proteoglycans were extracted from human gingiva with 2 M CaCl
2. The extracts were examined by gel filtration on Sephacryl S-400 in 2 M CaCl
2 under dissociative conditions. The 280 nm absorbance profiles of clinically uninflamed, inflamed and severely-inflamed tissues showed that material was present with molecular weights of between 2 × 10
6 or greater, and 16,000. Proteoglycans were examined by cellulose-acetate electrophoresis with subsequent identification of the constituent glycosaminoglycans after protease digestion, and finally by chondroitinase AC digestion of the liberated glycosaminoglycans. The relative proportion of each glycosaminoglycan was calculated by scanning each cellulose-acetate sheet on an integrating densitometer. Heparan sulphate was found only in fraction I (mol. wt 2 × 10
6 or greater), together with hyaluronic acid and chondroitin-4-sulphate, these being present in all of the glycosaminoglycan-containing fractions (I–1V). Dermatan sulphate was absent from fraction I, but present in II–IV, apparently existing on the same protein core as chondroitin-4-sulphate. The relative proportions of these two glycosaminoglycans was related to molecular size, and with the degree of inflammation for a given molecular species. |
doi_str_mv | 10.1016/0003-9969(84)90072-4 |
format | Article |
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2. The extracts were examined by gel filtration on Sephacryl S-400 in 2 M CaCl
2 under dissociative conditions. The 280 nm absorbance profiles of clinically uninflamed, inflamed and severely-inflamed tissues showed that material was present with molecular weights of between 2 × 10
6 or greater, and 16,000. Proteoglycans were examined by cellulose-acetate electrophoresis with subsequent identification of the constituent glycosaminoglycans after protease digestion, and finally by chondroitinase AC digestion of the liberated glycosaminoglycans. The relative proportion of each glycosaminoglycan was calculated by scanning each cellulose-acetate sheet on an integrating densitometer. Heparan sulphate was found only in fraction I (mol. wt 2 × 10
6 or greater), together with hyaluronic acid and chondroitin-4-sulphate, these being present in all of the glycosaminoglycan-containing fractions (I–1V). Dermatan sulphate was absent from fraction I, but present in II–IV, apparently existing on the same protein core as chondroitin-4-sulphate. The relative proportions of these two glycosaminoglycans was related to molecular size, and with the degree of inflammation for a given molecular species.</description><identifier>ISSN: 0003-9969</identifier><identifier>EISSN: 1879-1506</identifier><identifier>DOI: 10.1016/0003-9969(84)90072-4</identifier><identifier>PMID: 6433862</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Chondroitin Sulfates - analysis ; Chromatography, Gel ; Dentistry ; Dermatan Sulfate - analysis ; Electrophoresis, Cellulose Acetate ; Gingiva - analysis ; Gingivitis - metabolism ; Glycosaminoglycans - analysis ; Heparitin Sulfate - analysis ; Humans ; Hyaluronic Acid - analysis ; Proteoglycans - analysis</subject><ispartof>Archives of oral biology, 1984, Vol.29 (7), p.513-519</ispartof><rights>1984</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c452t-90ce54c416c2fea21efd355bcd4dc1be2cca8ddfe2cadef8cc23f8a215d937ee3</citedby><cites>FETCH-LOGICAL-c452t-90ce54c416c2fea21efd355bcd4dc1be2cca8ddfe2cadef8cc23f8a215d937ee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0003-9969(84)90072-4$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,4012,27906,27907,27908,45978</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6433862$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Purvis, J.A.</creatorcontrib><creatorcontrib>Embery, G.</creatorcontrib><creatorcontrib>Oliver, W.M.</creatorcontrib><title>Molecular size distribution of proteoglycans in human inflamed gingival tissue</title><title>Archives of oral biology</title><addtitle>Arch Oral Biol</addtitle><description>Proteoglycans were extracted from human gingiva with 2 M CaCl
2. The extracts were examined by gel filtration on Sephacryl S-400 in 2 M CaCl
2 under dissociative conditions. The 280 nm absorbance profiles of clinically uninflamed, inflamed and severely-inflamed tissues showed that material was present with molecular weights of between 2 × 10
6 or greater, and 16,000. Proteoglycans were examined by cellulose-acetate electrophoresis with subsequent identification of the constituent glycosaminoglycans after protease digestion, and finally by chondroitinase AC digestion of the liberated glycosaminoglycans. The relative proportion of each glycosaminoglycan was calculated by scanning each cellulose-acetate sheet on an integrating densitometer. Heparan sulphate was found only in fraction I (mol. wt 2 × 10
6 or greater), together with hyaluronic acid and chondroitin-4-sulphate, these being present in all of the glycosaminoglycan-containing fractions (I–1V). Dermatan sulphate was absent from fraction I, but present in II–IV, apparently existing on the same protein core as chondroitin-4-sulphate. The relative proportions of these two glycosaminoglycans was related to molecular size, and with the degree of inflammation for a given molecular species.</description><subject>Chondroitin Sulfates - analysis</subject><subject>Chromatography, Gel</subject><subject>Dentistry</subject><subject>Dermatan Sulfate - analysis</subject><subject>Electrophoresis, Cellulose Acetate</subject><subject>Gingiva - analysis</subject><subject>Gingivitis - metabolism</subject><subject>Glycosaminoglycans - analysis</subject><subject>Heparitin Sulfate - analysis</subject><subject>Humans</subject><subject>Hyaluronic Acid - analysis</subject><subject>Proteoglycans - analysis</subject><issn>0003-9969</issn><issn>1879-1506</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMlOwzAQhi0EKmV5A5B8QnAI2ImTOhckVLFJBS5wtpzxuBhlKXZSqTw9Lq165DT_aP7ZPkLOOLvmjBc3jLEsKcuivJTiqmRskiZij4y5nJQJz1mxT8Y7yyE5CuErpnlR8BEZFSLLZJGOyetLVyMMtfY0uB-kxoXeu2roXdfSztKF73rs5vUKdBuoa-nn0Og2ClvrBg2du3bulrqmvQthwBNyYHUd8HQbj8nHw_379CmZvT0-T-9mCYg87ZOSAeYCBC8gtahTjtZkeV6BEQZ4hSmAlsbYKLRBKwHSzMroy02ZTRCzY3KxmRvv-x4w9KpxAbCudYvdEJTkaSakYNEoNkbwXQgerVp412i_UpypNUa1ZqTWjJQU6g-jErHtfDt_qOKbu6Ytt1i_3dQxPrl06FUAhy2gcR6hV6Zz_y_4BRzihHk</recordid><startdate>1984</startdate><enddate>1984</enddate><creator>Purvis, J.A.</creator><creator>Embery, G.</creator><creator>Oliver, W.M.</creator><general>Elsevier Ltd</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></search><sort><creationdate>1984</creationdate><title>Molecular size distribution of proteoglycans in human inflamed gingival tissue</title><author>Purvis, J.A. ; Embery, G. ; Oliver, W.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-90ce54c416c2fea21efd355bcd4dc1be2cca8ddfe2cadef8cc23f8a215d937ee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Chondroitin Sulfates - analysis</topic><topic>Chromatography, Gel</topic><topic>Dentistry</topic><topic>Dermatan Sulfate - analysis</topic><topic>Electrophoresis, Cellulose Acetate</topic><topic>Gingiva - analysis</topic><topic>Gingivitis - metabolism</topic><topic>Glycosaminoglycans - analysis</topic><topic>Heparitin Sulfate - analysis</topic><topic>Humans</topic><topic>Hyaluronic Acid - analysis</topic><topic>Proteoglycans - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Purvis, J.A.</creatorcontrib><creatorcontrib>Embery, G.</creatorcontrib><creatorcontrib>Oliver, W.M.</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>Archives of oral biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Purvis, J.A.</au><au>Embery, G.</au><au>Oliver, W.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular size distribution of proteoglycans in human inflamed gingival tissue</atitle><jtitle>Archives of oral biology</jtitle><addtitle>Arch Oral Biol</addtitle><date>1984</date><risdate>1984</risdate><volume>29</volume><issue>7</issue><spage>513</spage><epage>519</epage><pages>513-519</pages><issn>0003-9969</issn><eissn>1879-1506</eissn><abstract>Proteoglycans were extracted from human gingiva with 2 M CaCl
2. The extracts were examined by gel filtration on Sephacryl S-400 in 2 M CaCl
2 under dissociative conditions. The 280 nm absorbance profiles of clinically uninflamed, inflamed and severely-inflamed tissues showed that material was present with molecular weights of between 2 × 10
6 or greater, and 16,000. Proteoglycans were examined by cellulose-acetate electrophoresis with subsequent identification of the constituent glycosaminoglycans after protease digestion, and finally by chondroitinase AC digestion of the liberated glycosaminoglycans. The relative proportion of each glycosaminoglycan was calculated by scanning each cellulose-acetate sheet on an integrating densitometer. Heparan sulphate was found only in fraction I (mol. wt 2 × 10
6 or greater), together with hyaluronic acid and chondroitin-4-sulphate, these being present in all of the glycosaminoglycan-containing fractions (I–1V). Dermatan sulphate was absent from fraction I, but present in II–IV, apparently existing on the same protein core as chondroitin-4-sulphate. The relative proportions of these two glycosaminoglycans was related to molecular size, and with the degree of inflammation for a given molecular species.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>6433862</pmid><doi>10.1016/0003-9969(84)90072-4</doi><tpages>7</tpages></addata></record> |
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language | eng |
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source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Chondroitin Sulfates - analysis Chromatography, Gel Dentistry Dermatan Sulfate - analysis Electrophoresis, Cellulose Acetate Gingiva - analysis Gingivitis - metabolism Glycosaminoglycans - analysis Heparitin Sulfate - analysis Humans Hyaluronic Acid - analysis Proteoglycans - analysis |
title | Molecular size distribution of proteoglycans in human inflamed gingival tissue |
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