Differential expression of neuropsin and protease M/neurosin in oligodendrocytes after injury to the spinal cord
Neuropsin and protease M/neurosin are serine proteases expressed by neurons and glial cells, and serve a variety of functions in the central nervous system (CNS). The current study demonstrates changes in the expression of these proteases following hemisection of the mouse spinal cord. Within unlesi...
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Veröffentlicht in: | Glia 2004-11, Vol.48 (2), p.91-101 |
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description | Neuropsin and protease M/neurosin are serine proteases expressed by neurons and glial cells, and serve a variety of functions in the central nervous system (CNS). The current study demonstrates changes in the expression of these proteases following hemisection of the mouse spinal cord. Within unlesioned spinal cord, neuropsin mRNA expression was occasionally observed in the gray but not white matter, while the level of protease M/neurosin mRNA was higher in the white matter. After injury to the spinal cord, neuropsin mRNA expression was induced in the white matter in the area immediately adjacent to the lesion, peaking at 4 days post‐injury and disappearing by 14 days. Enhanced expression of protease M/neurosin mRNA was observed throughout the white and gray matter surrounding the lesion, peaking at 4 days and persisting for 14 days. Neuropsin mRNA was expressed predominantly by CNPase‐positive oligodendrocytes. Furthermore, most of these cells were also associated with immunoreactivity for protease M/neurosin protein. Within unlesioned spinal cord, most protease M/neurosin mRNA‐expressing cells were CNPase‐positive oligodendrocytes, and a substantial fraction of these cells also showed immunoreactivity for NG2, a marker for oligodendrocyte progenitors. After injury, protease M/neurosin mRNA expression within NG2‐positive cells was significantly decreased, while the constitutive expression in CNPase‐positive oligodendrocytes appeared to be preserved. These findings suggest that each subpopulation of oligodendrocytes based on the expression of neuropsin and protease M/neurosin has different roles in the response of the spinal cord to injury as well as in normal homeostasis. © 2004 Wiley‐Liss, Inc. |
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The current study demonstrates changes in the expression of these proteases following hemisection of the mouse spinal cord. Within unlesioned spinal cord, neuropsin mRNA expression was occasionally observed in the gray but not white matter, while the level of protease M/neurosin mRNA was higher in the white matter. After injury to the spinal cord, neuropsin mRNA expression was induced in the white matter in the area immediately adjacent to the lesion, peaking at 4 days post‐injury and disappearing by 14 days. Enhanced expression of protease M/neurosin mRNA was observed throughout the white and gray matter surrounding the lesion, peaking at 4 days and persisting for 14 days. Neuropsin mRNA was expressed predominantly by CNPase‐positive oligodendrocytes. Furthermore, most of these cells were also associated with immunoreactivity for protease M/neurosin protein. Within unlesioned spinal cord, most protease M/neurosin mRNA‐expressing cells were CNPase‐positive oligodendrocytes, and a substantial fraction of these cells also showed immunoreactivity for NG2, a marker for oligodendrocyte progenitors. After injury, protease M/neurosin mRNA expression within NG2‐positive cells was significantly decreased, while the constitutive expression in CNPase‐positive oligodendrocytes appeared to be preserved. These findings suggest that each subpopulation of oligodendrocytes based on the expression of neuropsin and protease M/neurosin has different roles in the response of the spinal cord to injury as well as in normal homeostasis. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 0894-1491</identifier><identifier>EISSN: 1098-1136</identifier><identifier>DOI: 10.1002/glia.20058</identifier><identifier>PMID: 15378660</identifier><identifier>CODEN: GLIAEJ</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>2',3'-Cyclic-Nucleotide Phosphodiesterases - metabolism ; Animals ; Antigens - metabolism ; Biological and medical sciences ; Biomarkers ; demyelination ; Disease Models, Animal ; Down-Regulation - genetics ; Fundamental and applied biological sciences. Psychology ; hemisection ; Homeostasis - genetics ; Immunohistochemistry ; Isolated neuron and nerve. Neuroglia ; Kallikreins - genetics ; Kallikreins - metabolism ; Mice ; Mice, Inbred BALB C ; Nerve Fibers, Myelinated - enzymology ; Nerve Fibers, Myelinated - pathology ; Nerve Regeneration - genetics ; Oligodendroglia - cytology ; Oligodendroglia - enzymology ; Proteoglycans - metabolism ; RNA, Messenger - metabolism ; Serine Endopeptidases - genetics ; serine protease ; spinal cord ; Spinal Cord - enzymology ; Spinal Cord - pathology ; Spinal Cord - physiopathology ; Spinal Cord Injuries - enzymology ; Spinal Cord Injuries - genetics ; Stem Cells - cytology ; Stem Cells - enzymology ; Time Factors ; Up-Regulation - genetics ; Vertebrates: nervous system and sense organs</subject><ispartof>Glia, 2004-11, Vol.48 (2), p.91-101</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4908-f93f57cd2268143ee6a386064c685f9dbb13161bd2c96b4333ea339e52b74903</citedby><cites>FETCH-LOGICAL-c4908-f93f57cd2268143ee6a386064c685f9dbb13161bd2c96b4333ea339e52b74903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fglia.20058$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fglia.20058$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16217602$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15378660$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Terayama, Ryuji</creatorcontrib><creatorcontrib>Bando, Yoshio</creatorcontrib><creatorcontrib>Takahashi, Takayuki</creatorcontrib><creatorcontrib>Yoshida, Shigetaka</creatorcontrib><title>Differential expression of neuropsin and protease M/neurosin in oligodendrocytes after injury to the spinal cord</title><title>Glia</title><addtitle>Glia</addtitle><description>Neuropsin and protease M/neurosin are serine proteases expressed by neurons and glial cells, and serve a variety of functions in the central nervous system (CNS). The current study demonstrates changes in the expression of these proteases following hemisection of the mouse spinal cord. Within unlesioned spinal cord, neuropsin mRNA expression was occasionally observed in the gray but not white matter, while the level of protease M/neurosin mRNA was higher in the white matter. After injury to the spinal cord, neuropsin mRNA expression was induced in the white matter in the area immediately adjacent to the lesion, peaking at 4 days post‐injury and disappearing by 14 days. Enhanced expression of protease M/neurosin mRNA was observed throughout the white and gray matter surrounding the lesion, peaking at 4 days and persisting for 14 days. Neuropsin mRNA was expressed predominantly by CNPase‐positive oligodendrocytes. Furthermore, most of these cells were also associated with immunoreactivity for protease M/neurosin protein. Within unlesioned spinal cord, most protease M/neurosin mRNA‐expressing cells were CNPase‐positive oligodendrocytes, and a substantial fraction of these cells also showed immunoreactivity for NG2, a marker for oligodendrocyte progenitors. After injury, protease M/neurosin mRNA expression within NG2‐positive cells was significantly decreased, while the constitutive expression in CNPase‐positive oligodendrocytes appeared to be preserved. These findings suggest that each subpopulation of oligodendrocytes based on the expression of neuropsin and protease M/neurosin has different roles in the response of the spinal cord to injury as well as in normal homeostasis. © 2004 Wiley‐Liss, Inc.</description><subject>2',3'-Cyclic-Nucleotide Phosphodiesterases - metabolism</subject><subject>Animals</subject><subject>Antigens - metabolism</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>demyelination</subject><subject>Disease Models, Animal</subject><subject>Down-Regulation - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>hemisection</subject><subject>Homeostasis - genetics</subject><subject>Immunohistochemistry</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>Kallikreins - genetics</subject><subject>Kallikreins - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Nerve Fibers, Myelinated - enzymology</subject><subject>Nerve Fibers, Myelinated - pathology</subject><subject>Nerve Regeneration - genetics</subject><subject>Oligodendroglia - cytology</subject><subject>Oligodendroglia - enzymology</subject><subject>Proteoglycans - metabolism</subject><subject>RNA, Messenger - metabolism</subject><subject>Serine Endopeptidases - genetics</subject><subject>serine protease</subject><subject>spinal cord</subject><subject>Spinal Cord - enzymology</subject><subject>Spinal Cord - pathology</subject><subject>Spinal Cord - physiopathology</subject><subject>Spinal Cord Injuries - enzymology</subject><subject>Spinal Cord Injuries - genetics</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - enzymology</subject><subject>Time Factors</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>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkV9vFCEUxYnR2G31xQ9geNGHJtPyZwaGx7rqtrpqTJr4SBjmUqmzMMJM7H572e5q3zQhIXB_95wLB6EXlJxRQtj5zeDNGSOkaR-hBSWqrSjl4jFakFbVFa0VPULHOd8SQstBPkVHtOGyFYIs0PjWOwcJwuTNgOFuTJCzjwFHhwPMKY7ZB2xCj8cUJzAZ8Kfz-8Luvqw4-JvYQ-hTtNsJMjZuglQqt3Pa4ini6TvgPPpQ5G1M_TP0xJkhw_PDfoKu37-7Xl5W6y-rq-XFurK1Im3lFHeNtD1joqU1BxCGt4KI2oq2carvOsqpoF3PrBJdzTkHw7mChnWyCPAT9HovW8b-OUOe9MZnC8NgAsQ5ayEKxKT4L8iKZxlhp3i6B215e07g9Jj8xqStpkTvctC7HPR9DgV-eVCduw30D-jh4wvw6gCYbM3gkgnW5wdOMCoFYYWje-6XH2D7D0u9Wl9d_DGv9j0-T3D3t8ekH1pILhv97fNKv_n4QX5dXS614r8B6a-vxg</recordid><startdate>20041101</startdate><enddate>20041101</enddate><creator>Terayama, Ryuji</creator><creator>Bando, Yoshio</creator><creator>Takahashi, Takayuki</creator><creator>Yoshida, Shigetaka</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>20041101</creationdate><title>Differential expression of neuropsin and protease M/neurosin in oligodendrocytes after injury to the spinal cord</title><author>Terayama, Ryuji ; Bando, Yoshio ; Takahashi, Takayuki ; Yoshida, Shigetaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4908-f93f57cd2268143ee6a386064c685f9dbb13161bd2c96b4333ea339e52b74903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>2',3'-Cyclic-Nucleotide Phosphodiesterases - metabolism</topic><topic>Animals</topic><topic>Antigens - metabolism</topic><topic>Biological and medical sciences</topic><topic>Biomarkers</topic><topic>demyelination</topic><topic>Disease Models, Animal</topic><topic>Down-Regulation - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>hemisection</topic><topic>Homeostasis - genetics</topic><topic>Immunohistochemistry</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>Kallikreins - genetics</topic><topic>Kallikreins - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Nerve Fibers, Myelinated - enzymology</topic><topic>Nerve Fibers, Myelinated - pathology</topic><topic>Nerve Regeneration - genetics</topic><topic>Oligodendroglia - cytology</topic><topic>Oligodendroglia - enzymology</topic><topic>Proteoglycans - metabolism</topic><topic>RNA, Messenger - metabolism</topic><topic>Serine Endopeptidases - genetics</topic><topic>serine protease</topic><topic>spinal cord</topic><topic>Spinal Cord - enzymology</topic><topic>Spinal Cord - pathology</topic><topic>Spinal Cord - physiopathology</topic><topic>Spinal Cord Injuries - enzymology</topic><topic>Spinal Cord Injuries - genetics</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - enzymology</topic><topic>Time Factors</topic><topic>Up-Regulation - genetics</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Terayama, Ryuji</creatorcontrib><creatorcontrib>Bando, Yoshio</creatorcontrib><creatorcontrib>Takahashi, Takayuki</creatorcontrib><creatorcontrib>Yoshida, Shigetaka</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Glia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Terayama, Ryuji</au><au>Bando, Yoshio</au><au>Takahashi, Takayuki</au><au>Yoshida, Shigetaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential expression of neuropsin and protease M/neurosin in oligodendrocytes after injury to the spinal cord</atitle><jtitle>Glia</jtitle><addtitle>Glia</addtitle><date>2004-11-01</date><risdate>2004</risdate><volume>48</volume><issue>2</issue><spage>91</spage><epage>101</epage><pages>91-101</pages><issn>0894-1491</issn><eissn>1098-1136</eissn><coden>GLIAEJ</coden><abstract>Neuropsin and protease M/neurosin are serine proteases expressed by neurons and glial cells, and serve a variety of functions in the central nervous system (CNS). The current study demonstrates changes in the expression of these proteases following hemisection of the mouse spinal cord. Within unlesioned spinal cord, neuropsin mRNA expression was occasionally observed in the gray but not white matter, while the level of protease M/neurosin mRNA was higher in the white matter. After injury to the spinal cord, neuropsin mRNA expression was induced in the white matter in the area immediately adjacent to the lesion, peaking at 4 days post‐injury and disappearing by 14 days. Enhanced expression of protease M/neurosin mRNA was observed throughout the white and gray matter surrounding the lesion, peaking at 4 days and persisting for 14 days. Neuropsin mRNA was expressed predominantly by CNPase‐positive oligodendrocytes. Furthermore, most of these cells were also associated with immunoreactivity for protease M/neurosin protein. Within unlesioned spinal cord, most protease M/neurosin mRNA‐expressing cells were CNPase‐positive oligodendrocytes, and a substantial fraction of these cells also showed immunoreactivity for NG2, a marker for oligodendrocyte progenitors. After injury, protease M/neurosin mRNA expression within NG2‐positive cells was significantly decreased, while the constitutive expression in CNPase‐positive oligodendrocytes appeared to be preserved. These findings suggest that each subpopulation of oligodendrocytes based on the expression of neuropsin and protease M/neurosin has different roles in the response of the spinal cord to injury as well as in normal homeostasis. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15378660</pmid><doi>10.1002/glia.20058</doi><tpages>11</tpages></addata></record> |
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subjects | 2',3'-Cyclic-Nucleotide Phosphodiesterases - metabolism Animals Antigens - metabolism Biological and medical sciences Biomarkers demyelination Disease Models, Animal Down-Regulation - genetics Fundamental and applied biological sciences. Psychology hemisection Homeostasis - genetics Immunohistochemistry Isolated neuron and nerve. Neuroglia Kallikreins - genetics Kallikreins - metabolism Mice Mice, Inbred BALB C Nerve Fibers, Myelinated - enzymology Nerve Fibers, Myelinated - pathology Nerve Regeneration - genetics Oligodendroglia - cytology Oligodendroglia - enzymology Proteoglycans - metabolism RNA, Messenger - metabolism Serine Endopeptidases - genetics serine protease spinal cord Spinal Cord - enzymology Spinal Cord - pathology Spinal Cord - physiopathology Spinal Cord Injuries - enzymology Spinal Cord Injuries - genetics Stem Cells - cytology Stem Cells - enzymology Time Factors Up-Regulation - genetics Vertebrates: nervous system and sense organs |
title | Differential expression of neuropsin and protease M/neurosin in oligodendrocytes after injury to the spinal cord |
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