Normal labor associated with changes in uterine heparan sulfate proteoglycan expression and localization

Hypothesis: Proteoglycans are well-known modulators of intercellular communication and signaling. Remodeling of the proteoglycans in the human uterus occurs throughout pregnancy, and during labor. We therefore hypothesize that heparan sulfate proteoglycans (HSPGs) play an important role in establish...

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Veröffentlicht in:Acta obstetricia et gynecologica Scandinavica 2005-03, Vol.84 (3), p.217-224
Hauptverfasser: Cluff, Ann Hjelm, Malmström, Anders, Tingåker, Berith, David, Guido, Ekman-Ordeberg, Gunvor
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container_start_page 217
container_title Acta obstetricia et gynecologica Scandinavica
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creator Cluff, Ann Hjelm
Malmström, Anders
Tingåker, Berith
David, Guido
Ekman-Ordeberg, Gunvor
description Hypothesis: Proteoglycans are well-known modulators of intercellular communication and signaling. Remodeling of the proteoglycans in the human uterus occurs throughout pregnancy, and during labor. We therefore hypothesize that heparan sulfate proteoglycans (HSPGs) play an important role in establishing normal labor. In this study HSPGs were characterized and localized in human uterine tissue. Methods: Uterine biopsies were obtained from four nonpregnant women, four women during elective cesarean section and four during emergency cesarean section. The biopsies were extracted using 4 mguanidinium hydrochloride (GuHCL). HSPGs were then purified by repeated ion-exchange chromatography on dehydroepiandrosterone (DEAE)-cellulose after digestion with chondroitinase ABC and finally precipitated with Alcian blue. HSPGs were identified by agarose gel electrophoresis and Western blotting. Controlled degradation of the heparan sulfate (HS) side-chains was performed using heparitinase or deglycosylation with trifluoromethanesulfonic acid (TFMS). The resulting core proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and visualized by Coomassie staining. HSPGs were localized in uterine tissue by immunohistochemistry. Results: SDS-PAGE after deglycosylation indicated the presence of multiple distinct core proteins tentatively identified as syndecans 1-4 and glypican 1. Western blots confirmed the presence of these proteoglycans and also perlecan. Immunohistochemistry revealed that the HSPGs were localized mainly in the smooth muscle with few in the extracellular matrix (ECM). Syndecan 3, the dominant proteoglycan, showed the most pronounced changes during pregnancy and labor. Conclusion: For the first time several heparan sulfate proteoglycans have been identified and localized in the human uterus and shown to vary in expression during pregnancy and labor. Syndecan 3 had the most outstanding features in this respect.
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Remodeling of the proteoglycans in the human uterus occurs throughout pregnancy, and during labor. We therefore hypothesize that heparan sulfate proteoglycans (HSPGs) play an important role in establishing normal labor. In this study HSPGs were characterized and localized in human uterine tissue. Methods: Uterine biopsies were obtained from four nonpregnant women, four women during elective cesarean section and four during emergency cesarean section. The biopsies were extracted using 4 mguanidinium hydrochloride (GuHCL). HSPGs were then purified by repeated ion-exchange chromatography on dehydroepiandrosterone (DEAE)-cellulose after digestion with chondroitinase ABC and finally precipitated with Alcian blue. HSPGs were identified by agarose gel electrophoresis and Western blotting. Controlled degradation of the heparan sulfate (HS) side-chains was performed using heparitinase or deglycosylation with trifluoromethanesulfonic acid (TFMS). The resulting core proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and visualized by Coomassie staining. HSPGs were localized in uterine tissue by immunohistochemistry. Results: SDS-PAGE after deglycosylation indicated the presence of multiple distinct core proteins tentatively identified as syndecans 1-4 and glypican 1. Western blots confirmed the presence of these proteoglycans and also perlecan. Immunohistochemistry revealed that the HSPGs were localized mainly in the smooth muscle with few in the extracellular matrix (ECM). Syndecan 3, the dominant proteoglycan, showed the most pronounced changes during pregnancy and labor. Conclusion: For the first time several heparan sulfate proteoglycans have been identified and localized in the human uterus and shown to vary in expression during pregnancy and labor. 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Obstetrics ; Heparan Sulfate Proteoglycans - isolation &amp; purification ; Heparan Sulfate Proteoglycans - physiology ; Heparitin Sulfate - metabolism ; Humans ; Immunohistochemistry ; Labor, Obstetric - metabolism ; Labor, Obstetric - physiology ; Medical sciences ; Membrane Glycoproteins - metabolism ; Middle Aged ; Muscle, Smooth - metabolism ; Pregnancy ; Proteoglycans - metabolism ; Syndecan-3 ; Uterine Contraction - physiology ; Uterus - metabolism</subject><ispartof>Acta obstetricia et gynecologica Scandinavica, 2005-03, Vol.84 (3), p.217-224</ispartof><rights>2005 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2005</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c332t-1a39d5a9148ed67eaea72fdca959c44230d35b29abe83340e2606b3774822a703</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16534599$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15715528$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cluff, Ann Hjelm</creatorcontrib><creatorcontrib>Malmström, Anders</creatorcontrib><creatorcontrib>Tingåker, Berith</creatorcontrib><creatorcontrib>David, Guido</creatorcontrib><creatorcontrib>Ekman-Ordeberg, Gunvor</creatorcontrib><title>Normal labor associated with changes in uterine heparan sulfate proteoglycan expression and localization</title><title>Acta obstetricia et gynecologica Scandinavica</title><addtitle>Acta Obstet Gynecol Scand</addtitle><description>Hypothesis: Proteoglycans are well-known modulators of intercellular communication and signaling. 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The resulting core proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and visualized by Coomassie staining. HSPGs were localized in uterine tissue by immunohistochemistry. Results: SDS-PAGE after deglycosylation indicated the presence of multiple distinct core proteins tentatively identified as syndecans 1-4 and glypican 1. Western blots confirmed the presence of these proteoglycans and also perlecan. Immunohistochemistry revealed that the HSPGs were localized mainly in the smooth muscle with few in the extracellular matrix (ECM). Syndecan 3, the dominant proteoglycan, showed the most pronounced changes during pregnancy and labor. Conclusion: For the first time several heparan sulfate proteoglycans have been identified and localized in the human uterus and shown to vary in expression during pregnancy and labor. 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Obstetrics</subject><subject>Heparan Sulfate Proteoglycans - isolation &amp; purification</subject><subject>Heparan Sulfate Proteoglycans - physiology</subject><subject>Heparitin Sulfate - metabolism</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Labor, Obstetric - metabolism</subject><subject>Labor, Obstetric - physiology</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Middle Aged</subject><subject>Muscle, Smooth - metabolism</subject><subject>Pregnancy</subject><subject>Proteoglycans - metabolism</subject><subject>Syndecan-3</subject><subject>Uterine Contraction - physiology</subject><subject>Uterus - metabolism</subject><issn>0001-6349</issn><issn>1600-0412</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi1ERZfCX0C-wC2LP_NxhKoFpAou5WxNnEnjldde7ERs-fV12BU9crJm9Lz2zGNCKGdbzlr2cbdljPGqlqrbCsZ0KVWrtscXZMNrxiqmuHhJNv-gS_I6512pRKPaV-SS64ZrLdoNmb7HtAdPPfQxUcg5WgczDvS3mydqJwgPmKkLdJkxuYB0wgMkCDQvfiwgPaQ4Y3zwj7Y08XhImLOLgUIYqI8WvPsDc2m8IRcj-Ixvz-cV-Xl7c3_9tbr78eXb9ae7ykop5oqD7AYNHVctDnWDgNCIcbDQ6c4qJSQbpO5FBz22UiqGomZ1L5uylxDQMHlFPpzuLYP9WjDPZu-yRe8hYFyyqRtVYkoWsD2BNsWcE47mkNwe0qPhzKyWzc6sAs0q0KyWzV_L5lii785vLP0eh-fgWWsB3p8ByEXBWIRZl5-5Wkulu65wn0-cC-P6DxOCnycLCc0uLikUUf-f5gmPLZzq</recordid><startdate>20050301</startdate><enddate>20050301</enddate><creator>Cluff, Ann Hjelm</creator><creator>Malmström, Anders</creator><creator>Tingåker, Berith</creator><creator>David, Guido</creator><creator>Ekman-Ordeberg, Gunvor</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</general><scope>IQODW</scope><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>20050301</creationdate><title>Normal labor associated with changes in uterine heparan sulfate proteoglycan expression and localization</title><author>Cluff, Ann Hjelm ; Malmström, Anders ; Tingåker, Berith ; David, Guido ; Ekman-Ordeberg, Gunvor</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c332t-1a39d5a9148ed67eaea72fdca959c44230d35b29abe83340e2606b3774822a703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Delivery. Postpartum. Lactation</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Female</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Heparan Sulfate Proteoglycans - isolation &amp; purification</topic><topic>Heparan Sulfate Proteoglycans - physiology</topic><topic>Heparitin Sulfate - metabolism</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Labor, Obstetric - metabolism</topic><topic>Labor, Obstetric - physiology</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins - metabolism</topic><topic>Middle Aged</topic><topic>Muscle, Smooth - metabolism</topic><topic>Pregnancy</topic><topic>Proteoglycans - metabolism</topic><topic>Syndecan-3</topic><topic>Uterine Contraction - physiology</topic><topic>Uterus - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cluff, Ann Hjelm</creatorcontrib><creatorcontrib>Malmström, Anders</creatorcontrib><creatorcontrib>Tingåker, Berith</creatorcontrib><creatorcontrib>David, Guido</creatorcontrib><creatorcontrib>Ekman-Ordeberg, Gunvor</creatorcontrib><collection>Pascal-Francis</collection><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>Acta obstetricia et gynecologica Scandinavica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cluff, Ann Hjelm</au><au>Malmström, Anders</au><au>Tingåker, Berith</au><au>David, Guido</au><au>Ekman-Ordeberg, Gunvor</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Normal labor associated with changes in uterine heparan sulfate proteoglycan expression and localization</atitle><jtitle>Acta obstetricia et gynecologica Scandinavica</jtitle><addtitle>Acta Obstet Gynecol Scand</addtitle><date>2005-03-01</date><risdate>2005</risdate><volume>84</volume><issue>3</issue><spage>217</spage><epage>224</epage><pages>217-224</pages><issn>0001-6349</issn><eissn>1600-0412</eissn><coden>AOGSAE</coden><abstract>Hypothesis: Proteoglycans are well-known modulators of intercellular communication and signaling. Remodeling of the proteoglycans in the human uterus occurs throughout pregnancy, and during labor. We therefore hypothesize that heparan sulfate proteoglycans (HSPGs) play an important role in establishing normal labor. In this study HSPGs were characterized and localized in human uterine tissue. Methods: Uterine biopsies were obtained from four nonpregnant women, four women during elective cesarean section and four during emergency cesarean section. The biopsies were extracted using 4 mguanidinium hydrochloride (GuHCL). HSPGs were then purified by repeated ion-exchange chromatography on dehydroepiandrosterone (DEAE)-cellulose after digestion with chondroitinase ABC and finally precipitated with Alcian blue. HSPGs were identified by agarose gel electrophoresis and Western blotting. Controlled degradation of the heparan sulfate (HS) side-chains was performed using heparitinase or deglycosylation with trifluoromethanesulfonic acid (TFMS). The resulting core proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and visualized by Coomassie staining. HSPGs were localized in uterine tissue by immunohistochemistry. Results: SDS-PAGE after deglycosylation indicated the presence of multiple distinct core proteins tentatively identified as syndecans 1-4 and glypican 1. Western blots confirmed the presence of these proteoglycans and also perlecan. Immunohistochemistry revealed that the HSPGs were localized mainly in the smooth muscle with few in the extracellular matrix (ECM). Syndecan 3, the dominant proteoglycan, showed the most pronounced changes during pregnancy and labor. Conclusion: For the first time several heparan sulfate proteoglycans have been identified and localized in the human uterus and shown to vary in expression during pregnancy and labor. Syndecan 3 had the most outstanding features in this respect.</abstract><cop>Colchester</cop><pub>Informa UK Ltd</pub><pmid>15715528</pmid><doi>10.1080/j.0001-6349.2005.00484.x</doi><tpages>8</tpages></addata></record>
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subjects Adult
Biological and medical sciences
Blotting, Western
Delivery. Postpartum. Lactation
Electrophoresis, Polyacrylamide Gel
Female
Gynecology. Andrology. Obstetrics
Heparan Sulfate Proteoglycans - isolation & purification
Heparan Sulfate Proteoglycans - physiology
Heparitin Sulfate - metabolism
Humans
Immunohistochemistry
Labor, Obstetric - metabolism
Labor, Obstetric - physiology
Medical sciences
Membrane Glycoproteins - metabolism
Middle Aged
Muscle, Smooth - metabolism
Pregnancy
Proteoglycans - metabolism
Syndecan-3
Uterine Contraction - physiology
Uterus - metabolism
title Normal labor associated with changes in uterine heparan sulfate proteoglycan expression and localization
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