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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
Main Authors: Iseki, Ken, Hagino, Seita, Mori, Tetsuji, Zhang, Yuxiang, Yokoya, Sachihiko, Takaki, Hiromi, Tase, Choichiro, Murakawa, Masahiro, Wanaka, Akio
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container_title Glia
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creator Iseki, Ken
Hagino, Seita
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Murakawa, Masahiro
Wanaka, Akio
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.
doi_str_mv 10.1002/glia.10078
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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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