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Increased syndecan expression by pleiotrophin and FGF receptor-expressing astrocytes in injured brain tissue
Syndecan‐1, ‐2, ‐3, and ‐4 are heparan sulfate proteoglycans that are differentially expressed during development and wound repair. To determine whether syndecans are also involved in brain injury, we examined the expression of syndecan core proteins genes in cryo‐injured mouse brain, using in situ...
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Published in: | Glia 2002-07, Vol.39 (1), p.1-9 |
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description | Syndecan‐1, ‐2, ‐3, and ‐4 are heparan sulfate proteoglycans that are differentially expressed during development and wound repair. To determine whether syndecans are also involved in brain injury, we examined the expression of syndecan core proteins genes in cryo‐injured mouse brain, using in situ hybridization. All syndecan mRNA transcripts were similarly expressed in the region surrounding the necrotic tissue, exhibiting peak levels at day 7 after injury. Comparison with cellular markers showed that reactive astrocytes were the primary source of syndecans. Syndecans serve as co‐receptors for fibroblast growth factor (FGF) and as a reservoir for another heparin‐binding growth factor, pleiotrophin (PTN, or heparin‐binding growth‐associated molecule. In our model, FGF receptor1 (FGFR1) and PTN mRNA levels were upregulated in reactive astrocytes. The distribution patterns of FGFR1 and PTN overlapped considerably with those of syndecan‐1 and ‐3 mRNAs, respectively. These results suggest that syndecans are expressed primarily in reactive astrocytes, and may provide a supportive environment for regenerating axons in concert with heparin‐binding growth factors (e.g., FGF and PTN) in the injured brain. GLIA 39:1–9, 2002. © 2002 Wiley‐Liss, Inc. |
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To determine whether syndecans are also involved in brain injury, we examined the expression of syndecan core proteins genes in cryo‐injured mouse brain, using in situ hybridization. All syndecan mRNA transcripts were similarly expressed in the region surrounding the necrotic tissue, exhibiting peak levels at day 7 after injury. Comparison with cellular markers showed that reactive astrocytes were the primary source of syndecans. Syndecans serve as co‐receptors for fibroblast growth factor (FGF) and as a reservoir for another heparin‐binding growth factor, pleiotrophin (PTN, or heparin‐binding growth‐associated molecule. In our model, FGF receptor1 (FGFR1) and PTN mRNA levels were upregulated in reactive astrocytes. The distribution patterns of FGFR1 and PTN overlapped considerably with those of syndecan‐1 and ‐3 mRNAs, respectively. These results suggest that syndecans are expressed primarily in reactive astrocytes, and may provide a supportive environment for regenerating axons in concert with heparin‐binding growth factors (e.g., FGF and PTN) in the injured brain. GLIA 39:1–9, 2002. © 2002 Wiley‐Liss, Inc.</description><identifier>ISSN: 0894-1491</identifier><identifier>EISSN: 1098-1136</identifier><identifier>DOI: 10.1002/glia.10078</identifier><identifier>PMID: 12112370</identifier><identifier>CODEN: GLIAEJ</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Astrocytes - metabolism ; Biological and medical sciences ; Brain Injuries - metabolism ; Brain Injuries - pathology ; brain injury ; Carrier Proteins - biosynthesis ; Carrier Proteins - genetics ; Cytokines - biosynthesis ; Cytokines - genetics ; FGF ; Fundamental and applied biological sciences. Psychology ; gliosis ; Isolated neuron and nerve. Neuroglia ; Male ; Membrane Glycoproteins - biosynthesis ; Membrane Glycoproteins - genetics ; Mice ; Mice, Inbred ICR ; pleiotrophin ; Proteoglycans - biosynthesis ; Proteoglycans - genetics ; reactive astrocyte ; Receptor Protein-Tyrosine Kinases - biosynthesis ; Receptor Protein-Tyrosine Kinases - genetics ; Receptor, Fibroblast Growth Factor, Type 1 ; Receptors, Fibroblast Growth Factor - biosynthesis ; Receptors, Fibroblast Growth Factor - genetics ; RNA, Messenger - biosynthesis ; syndecan ; Syndecan-1 ; Syndecans ; Up-Regulation - genetics ; Vertebrates: nervous system and sense organs</subject><ispartof>Glia, 2002-07, Vol.39 (1), p.1-9</ispartof><rights>Copyright © 2002 Wiley‐Liss, Inc.</rights><rights>2002 INIST-CNRS</rights><rights>Copyright 2002 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4598-1d84cfa722a9839b6a3197be5f8652ff2d435cf614d5a007c8803206ab92c4793</citedby><cites>FETCH-LOGICAL-c4598-1d84cfa722a9839b6a3197be5f8652ff2d435cf614d5a007c8803206ab92c4793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13742563$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12112370$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iseki, Ken</creatorcontrib><creatorcontrib>Hagino, Seita</creatorcontrib><creatorcontrib>Mori, Tetsuji</creatorcontrib><creatorcontrib>Zhang, Yuxiang</creatorcontrib><creatorcontrib>Yokoya, Sachihiko</creatorcontrib><creatorcontrib>Takaki, Hiromi</creatorcontrib><creatorcontrib>Tase, Choichiro</creatorcontrib><creatorcontrib>Murakawa, Masahiro</creatorcontrib><creatorcontrib>Wanaka, Akio</creatorcontrib><title>Increased syndecan expression by pleiotrophin and FGF receptor-expressing astrocytes in injured brain tissue</title><title>Glia</title><addtitle>Glia</addtitle><description>Syndecan‐1, ‐2, ‐3, and ‐4 are heparan sulfate proteoglycans that are differentially expressed during development and wound repair. To determine whether syndecans are also involved in brain injury, we examined the expression of syndecan core proteins genes in cryo‐injured mouse brain, using in situ hybridization. All syndecan mRNA transcripts were similarly expressed in the region surrounding the necrotic tissue, exhibiting peak levels at day 7 after injury. Comparison with cellular markers showed that reactive astrocytes were the primary source of syndecans. Syndecans serve as co‐receptors for fibroblast growth factor (FGF) and as a reservoir for another heparin‐binding growth factor, pleiotrophin (PTN, or heparin‐binding growth‐associated molecule. In our model, FGF receptor1 (FGFR1) and PTN mRNA levels were upregulated in reactive astrocytes. The distribution patterns of FGFR1 and PTN overlapped considerably with those of syndecan‐1 and ‐3 mRNAs, respectively. These results suggest that syndecans are expressed primarily in reactive astrocytes, and may provide a supportive environment for regenerating axons in concert with heparin‐binding growth factors (e.g., FGF and PTN) in the injured brain. GLIA 39:1–9, 2002. © 2002 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Astrocytes - metabolism</subject><subject>Biological and medical sciences</subject><subject>Brain Injuries - metabolism</subject><subject>Brain Injuries - pathology</subject><subject>brain injury</subject><subject>Carrier Proteins - biosynthesis</subject><subject>Carrier Proteins - genetics</subject><subject>Cytokines - biosynthesis</subject><subject>Cytokines - genetics</subject><subject>FGF</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gliosis</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>Male</subject><subject>Membrane Glycoproteins - biosynthesis</subject><subject>Membrane Glycoproteins - genetics</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>pleiotrophin</subject><subject>Proteoglycans - biosynthesis</subject><subject>Proteoglycans - genetics</subject><subject>reactive astrocyte</subject><subject>Receptor Protein-Tyrosine Kinases - biosynthesis</subject><subject>Receptor Protein-Tyrosine Kinases - genetics</subject><subject>Receptor, Fibroblast Growth Factor, Type 1</subject><subject>Receptors, Fibroblast Growth Factor - biosynthesis</subject><subject>Receptors, Fibroblast Growth Factor - genetics</subject><subject>RNA, Messenger - biosynthesis</subject><subject>syndecan</subject><subject>Syndecan-1</subject><subject>Syndecans</subject><subject>Up-Regulation - genetics</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0894-1491</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp90E1v1DAQBmALgehSuPADkC9wQAr4I4njY1XYZaUVqAi03CzHmRSXrJN6EtH8exx2S2-c7JGembFfQl5y9o4zJt5fd94uN1U9IivOdJVxLsvHZMUqnWc81_yMPEO8YYynQj0lZ1xwLqRiK9Jtg4tgERqKc2jA2UDhboiA6PtA65kOHfh-jP3w0wdqQ0PXmzWN4GAY-5jd23BNLSbl5hGQJunDzRTT1DraVI0ecYLn5ElrO4QXp_OcfF9__Hb5Kdt92WwvL3aZy4vl9U2Vu9YqIayupK5LK7lWNRRtVRaibUWTy8K1Jc-bwqZvu6piUrDS1lq4XGl5Tt4c5w6xv50AR3Pw6KDrbIB-QqN4pZckEnx7hC72iBFaM0R_sHE2nJklW7Nka_5mm_Cr09SpPkDzQE9hJvD6BCw627XRBufxwUmVi6KUyfGj--07mP-z0mx224v75dmxx-MId_96bPxlSiVVYfafN-br_sOPq6tyb5T8A-g-oaQ</recordid><startdate>200207</startdate><enddate>200207</enddate><creator>Iseki, Ken</creator><creator>Hagino, Seita</creator><creator>Mori, Tetsuji</creator><creator>Zhang, Yuxiang</creator><creator>Yokoya, Sachihiko</creator><creator>Takaki, Hiromi</creator><creator>Tase, Choichiro</creator><creator>Murakawa, Masahiro</creator><creator>Wanaka, Akio</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><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>200207</creationdate><title>Increased syndecan expression by pleiotrophin and FGF receptor-expressing astrocytes in injured brain tissue</title><author>Iseki, Ken ; Hagino, Seita ; Mori, Tetsuji ; Zhang, Yuxiang ; Yokoya, Sachihiko ; Takaki, Hiromi ; Tase, Choichiro ; Murakawa, Masahiro ; Wanaka, Akio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4598-1d84cfa722a9839b6a3197be5f8652ff2d435cf614d5a007c8803206ab92c4793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Astrocytes - metabolism</topic><topic>Biological and medical sciences</topic><topic>Brain Injuries - metabolism</topic><topic>Brain Injuries - pathology</topic><topic>brain injury</topic><topic>Carrier Proteins - biosynthesis</topic><topic>Carrier Proteins - genetics</topic><topic>Cytokines - biosynthesis</topic><topic>Cytokines - genetics</topic><topic>FGF</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gliosis</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>Male</topic><topic>Membrane Glycoproteins - biosynthesis</topic><topic>Membrane Glycoproteins - genetics</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>pleiotrophin</topic><topic>Proteoglycans - biosynthesis</topic><topic>Proteoglycans - genetics</topic><topic>reactive astrocyte</topic><topic>Receptor Protein-Tyrosine Kinases - biosynthesis</topic><topic>Receptor Protein-Tyrosine Kinases - genetics</topic><topic>Receptor, Fibroblast Growth Factor, Type 1</topic><topic>Receptors, Fibroblast Growth Factor - biosynthesis</topic><topic>Receptors, Fibroblast Growth Factor - genetics</topic><topic>RNA, Messenger - biosynthesis</topic><topic>syndecan</topic><topic>Syndecan-1</topic><topic>Syndecans</topic><topic>Up-Regulation - genetics</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iseki, Ken</creatorcontrib><creatorcontrib>Hagino, Seita</creatorcontrib><creatorcontrib>Mori, Tetsuji</creatorcontrib><creatorcontrib>Zhang, Yuxiang</creatorcontrib><creatorcontrib>Yokoya, Sachihiko</creatorcontrib><creatorcontrib>Takaki, Hiromi</creatorcontrib><creatorcontrib>Tase, Choichiro</creatorcontrib><creatorcontrib>Murakawa, Masahiro</creatorcontrib><creatorcontrib>Wanaka, Akio</creatorcontrib><collection>Istex</collection><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>Glia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iseki, Ken</au><au>Hagino, Seita</au><au>Mori, Tetsuji</au><au>Zhang, Yuxiang</au><au>Yokoya, Sachihiko</au><au>Takaki, Hiromi</au><au>Tase, Choichiro</au><au>Murakawa, Masahiro</au><au>Wanaka, Akio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased syndecan expression by pleiotrophin and FGF receptor-expressing astrocytes in injured brain tissue</atitle><jtitle>Glia</jtitle><addtitle>Glia</addtitle><date>2002-07</date><risdate>2002</risdate><volume>39</volume><issue>1</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>0894-1491</issn><eissn>1098-1136</eissn><coden>GLIAEJ</coden><abstract>Syndecan‐1, ‐2, ‐3, and ‐4 are heparan sulfate proteoglycans that are differentially expressed during development and wound repair. To determine whether syndecans are also involved in brain injury, we examined the expression of syndecan core proteins genes in cryo‐injured mouse brain, using in situ hybridization. All syndecan mRNA transcripts were similarly expressed in the region surrounding the necrotic tissue, exhibiting peak levels at day 7 after injury. Comparison with cellular markers showed that reactive astrocytes were the primary source of syndecans. Syndecans serve as co‐receptors for fibroblast growth factor (FGF) and as a reservoir for another heparin‐binding growth factor, pleiotrophin (PTN, or heparin‐binding growth‐associated molecule. In our model, FGF receptor1 (FGFR1) and PTN mRNA levels were upregulated in reactive astrocytes. The distribution patterns of FGFR1 and PTN overlapped considerably with those of syndecan‐1 and ‐3 mRNAs, respectively. These results suggest that syndecans are expressed primarily in reactive astrocytes, and may provide a supportive environment for regenerating axons in concert with heparin‐binding growth factors (e.g., FGF and PTN) in the injured brain. GLIA 39:1–9, 2002. © 2002 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12112370</pmid><doi>10.1002/glia.10078</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Astrocytes - metabolism Biological and medical sciences Brain Injuries - metabolism Brain Injuries - pathology brain injury Carrier Proteins - biosynthesis Carrier Proteins - genetics Cytokines - biosynthesis Cytokines - genetics FGF Fundamental and applied biological sciences. Psychology gliosis Isolated neuron and nerve. Neuroglia Male Membrane Glycoproteins - biosynthesis Membrane Glycoproteins - genetics Mice Mice, Inbred ICR pleiotrophin Proteoglycans - biosynthesis Proteoglycans - genetics reactive astrocyte Receptor Protein-Tyrosine Kinases - biosynthesis Receptor Protein-Tyrosine Kinases - genetics Receptor, Fibroblast Growth Factor, Type 1 Receptors, Fibroblast Growth Factor - biosynthesis Receptors, Fibroblast Growth Factor - genetics RNA, Messenger - biosynthesis syndecan Syndecan-1 Syndecans Up-Regulation - genetics Vertebrates: nervous system and sense organs |
title | Increased syndecan expression by pleiotrophin and FGF receptor-expressing astrocytes in injured brain tissue |
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