Mature myelin basic protein-expressing oligodendrocytes are insensitive to kainate toxicity
We examined the vulnerability to excitotoxicity of rat oligodendrocytes in dissociated cell culture at different developmental stages. Mature oligodendrocytes that express myelin basic protein were resistant to excitotoxic injury produced by kainate, whereas earlier stages in the oligodendrocyte lin...
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Veröffentlicht in: | Journal of neuroscience research 2003-01, Vol.71 (2), p.237-245 |
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creator | Rosenberg, Paul A. Dai, Weimin Gan, Xiao Dong Ali, Sanjida Fu, Jennifer Back, Stephen A. Sanchez, Russell M. Segal, Michael M. Follett, Pamela L. Jensen, Frances E. Volpe, Joseph J. |
description | We examined the vulnerability to excitotoxicity of rat oligodendrocytes in dissociated cell culture at different developmental stages. Mature oligodendrocytes that express myelin basic protein were resistant to excitotoxic injury produced by kainate, whereas earlier stages in the oligodendrocyte lineage were vulnerable to this insult. To test the hypothesis that the sensitivity of immature oligodendrocytes and the resistance of mature oligodendrocytes to kainate toxicity were due to differences in membrane responsiveness to kainate, we used whole‐cell patch‐clamp recording. Oligodendrocyte precursors in cultures vulnerable to kainate toxicity responded to 500 μM kainate with large inward currents, whereas mature myelin basic protein‐expressing oligodendrocytes in cultures resistant to kainate toxicity showed no clear response to application of this agonist. We assayed expression of glutamate receptor subunits (GluR) ‐2, ‐4, ‐6, ‐7, and KA2 using immunoblot analysis and found that expression of all of these glutamate receptors was significantly down‐regulated in mature oligodendrocytes. These results suggest a striking developmental regulation of glutamate receptors in oligodendrocytes and suggest that the vulnerability of oligodendrocytes to non‐ N‐methyl‐D‐aspartate receptor‐mediated excitotoxicity might be much greater in developing oligodendrocytes than after the completion of myelination. © 2002 Wiley‐Liss, Inc. |
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Mature oligodendrocytes that express myelin basic protein were resistant to excitotoxic injury produced by kainate, whereas earlier stages in the oligodendrocyte lineage were vulnerable to this insult. To test the hypothesis that the sensitivity of immature oligodendrocytes and the resistance of mature oligodendrocytes to kainate toxicity were due to differences in membrane responsiveness to kainate, we used whole‐cell patch‐clamp recording. Oligodendrocyte precursors in cultures vulnerable to kainate toxicity responded to 500 μM kainate with large inward currents, whereas mature myelin basic protein‐expressing oligodendrocytes in cultures resistant to kainate toxicity showed no clear response to application of this agonist. We assayed expression of glutamate receptor subunits (GluR) ‐2, ‐4, ‐6, ‐7, and KA2 using immunoblot analysis and found that expression of all of these glutamate receptors was significantly down‐regulated in mature oligodendrocytes. These results suggest a striking developmental regulation of glutamate receptors in oligodendrocytes and suggest that the vulnerability of oligodendrocytes to non‐ N‐methyl‐D‐aspartate receptor‐mediated excitotoxicity might be much greater in developing oligodendrocytes than after the completion of myelination. © 2002 Wiley‐Liss, Inc.</description><identifier>ISSN: 0360-4012</identifier><identifier>EISSN: 1097-4547</identifier><identifier>DOI: 10.1002/jnr.10472</identifier><identifier>PMID: 12503086</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology ; alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology ; Animals ; Animals, Newborn ; Cell Culture Techniques ; Cell Differentiation - drug effects ; Cell Differentiation - physiology ; Cell Survival - drug effects ; cerebral palsy ; Ciliary Neurotrophic Factor - pharmacology ; Dose-Response Relationship, Drug ; Down-Regulation ; Drug Interactions ; Electrophysiology - methods ; Excitatory Amino Acid Agonists - pharmacology ; Excitatory Amino Acid Antagonists - pharmacology ; excitotoxicity ; Fibroblast Growth Factors - pharmacology ; glutamate ; hypoxia ; Immunoblotting ; Immunohistochemistry ; ischemia ; Kainic Acid - pharmacology ; Myelin Basic Protein - drug effects ; Myelin Basic Protein - metabolism ; Oligodendroglia - drug effects ; Oligodendroglia - metabolism ; periventricular leukomalacia ; Platelet-Derived Growth Factor - pharmacology ; Rats ; Rats, Sprague-Dawley ; Receptors, Glutamate - classification ; Receptors, Glutamate - metabolism</subject><ispartof>Journal of neuroscience research, 2003-01, Vol.71 (2), p.237-245</ispartof><rights>Copyright © 2002 Wiley‐Liss, Inc.</rights><rights>Copyright 2002 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4082-4abd0f9586d99d3a422ab185967aa79b8867e983dd86e2d49ba8613cd6f690cc3</citedby><cites>FETCH-LOGICAL-c4082-4abd0f9586d99d3a422ab185967aa79b8867e983dd86e2d49ba8613cd6f690cc3</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%2Fjnr.10472$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjnr.10472$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12503086$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rosenberg, Paul A.</creatorcontrib><creatorcontrib>Dai, Weimin</creatorcontrib><creatorcontrib>Gan, Xiao Dong</creatorcontrib><creatorcontrib>Ali, Sanjida</creatorcontrib><creatorcontrib>Fu, Jennifer</creatorcontrib><creatorcontrib>Back, Stephen A.</creatorcontrib><creatorcontrib>Sanchez, Russell M.</creatorcontrib><creatorcontrib>Segal, Michael M.</creatorcontrib><creatorcontrib>Follett, Pamela L.</creatorcontrib><creatorcontrib>Jensen, Frances E.</creatorcontrib><creatorcontrib>Volpe, Joseph J.</creatorcontrib><title>Mature myelin basic protein-expressing oligodendrocytes are insensitive to kainate toxicity</title><title>Journal of neuroscience research</title><addtitle>J. Neurosci. Res</addtitle><description>We examined the vulnerability to excitotoxicity of rat oligodendrocytes in dissociated cell culture at different developmental stages. Mature oligodendrocytes that express myelin basic protein were resistant to excitotoxic injury produced by kainate, whereas earlier stages in the oligodendrocyte lineage were vulnerable to this insult. To test the hypothesis that the sensitivity of immature oligodendrocytes and the resistance of mature oligodendrocytes to kainate toxicity were due to differences in membrane responsiveness to kainate, we used whole‐cell patch‐clamp recording. Oligodendrocyte precursors in cultures vulnerable to kainate toxicity responded to 500 μM kainate with large inward currents, whereas mature myelin basic protein‐expressing oligodendrocytes in cultures resistant to kainate toxicity showed no clear response to application of this agonist. We assayed expression of glutamate receptor subunits (GluR) ‐2, ‐4, ‐6, ‐7, and KA2 using immunoblot analysis and found that expression of all of these glutamate receptors was significantly down‐regulated in mature oligodendrocytes. These results suggest a striking developmental regulation of glutamate receptors in oligodendrocytes and suggest that the vulnerability of oligodendrocytes to non‐ N‐methyl‐D‐aspartate receptor‐mediated excitotoxicity might be much greater in developing oligodendrocytes than after the completion of myelination. © 2002 Wiley‐Liss, Inc.</description><subject>6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology</subject><subject>alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Cell Culture Techniques</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Survival - drug effects</subject><subject>cerebral palsy</subject><subject>Ciliary Neurotrophic Factor - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Down-Regulation</subject><subject>Drug Interactions</subject><subject>Electrophysiology - methods</subject><subject>Excitatory Amino Acid Agonists - pharmacology</subject><subject>Excitatory Amino Acid Antagonists - pharmacology</subject><subject>excitotoxicity</subject><subject>Fibroblast Growth Factors - pharmacology</subject><subject>glutamate</subject><subject>hypoxia</subject><subject>Immunoblotting</subject><subject>Immunohistochemistry</subject><subject>ischemia</subject><subject>Kainic Acid - pharmacology</subject><subject>Myelin Basic Protein - drug effects</subject><subject>Myelin Basic Protein - metabolism</subject><subject>Oligodendroglia - drug effects</subject><subject>Oligodendroglia - metabolism</subject><subject>periventricular leukomalacia</subject><subject>Platelet-Derived Growth Factor - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Glutamate - classification</subject><subject>Receptors, Glutamate - metabolism</subject><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMFuEzEURS1UREJg0R-oZlWJxdBne8ZjLyGCAApFQqAisbA89kvkduJJbQcyf8-EpGXF6t3FuUdPl5BzCq8pALu6DXEMVcOekCkF1ZRVXTVnZApcQFkBZRPyPKVbAFCq5s_IhLIaOEgxJT8_m7yLWGwG7HwoWpO8Lbaxz-hDifttxJR8WBd959e9w-Bib4eMqTBjyYeEIfnsf2GR--LO-GDyIe699Xl4QZ6uTJfw5enOyPf3777NP5TLL4uP8zfL0lYgWVmZ1sFK1VI4pRw3FWOmpbJWojGmUa2UokEluXNSIHOVao0UlFsnVkKBtXxGLo_e8e_7HaasNz5Z7DoTsN8lTaUQQCUbwVdH0MY-pYgrvY1-Y-KgKejDknpcUv9dcmQvTtJdu0H3jzxNNwJXR-C373D4v0l_uv76oCyPDZ8y7h8bJt5p0fCm1jfXCy2XPxRd3rzVC_4H5aeOOA</recordid><startdate>20030115</startdate><enddate>20030115</enddate><creator>Rosenberg, Paul A.</creator><creator>Dai, Weimin</creator><creator>Gan, Xiao Dong</creator><creator>Ali, Sanjida</creator><creator>Fu, Jennifer</creator><creator>Back, Stephen A.</creator><creator>Sanchez, Russell M.</creator><creator>Segal, Michael M.</creator><creator>Follett, Pamela L.</creator><creator>Jensen, Frances E.</creator><creator>Volpe, Joseph J.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>20030115</creationdate><title>Mature myelin basic protein-expressing oligodendrocytes are insensitive to kainate toxicity</title><author>Rosenberg, Paul A. ; Dai, Weimin ; Gan, Xiao Dong ; Ali, Sanjida ; Fu, Jennifer ; Back, Stephen A. ; Sanchez, Russell M. ; Segal, Michael M. ; Follett, Pamela L. ; Jensen, Frances E. ; Volpe, Joseph J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4082-4abd0f9586d99d3a422ab185967aa79b8867e983dd86e2d49ba8613cd6f690cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology</topic><topic>alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Cell Culture Techniques</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Differentiation - physiology</topic><topic>Cell Survival - drug effects</topic><topic>cerebral palsy</topic><topic>Ciliary Neurotrophic Factor - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Down-Regulation</topic><topic>Drug Interactions</topic><topic>Electrophysiology - methods</topic><topic>Excitatory Amino Acid Agonists - pharmacology</topic><topic>Excitatory Amino Acid Antagonists - pharmacology</topic><topic>excitotoxicity</topic><topic>Fibroblast Growth Factors - pharmacology</topic><topic>glutamate</topic><topic>hypoxia</topic><topic>Immunoblotting</topic><topic>Immunohistochemistry</topic><topic>ischemia</topic><topic>Kainic Acid - pharmacology</topic><topic>Myelin Basic Protein - drug effects</topic><topic>Myelin Basic Protein - metabolism</topic><topic>Oligodendroglia - drug effects</topic><topic>Oligodendroglia - metabolism</topic><topic>periventricular leukomalacia</topic><topic>Platelet-Derived Growth Factor - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Glutamate - classification</topic><topic>Receptors, Glutamate - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rosenberg, Paul A.</creatorcontrib><creatorcontrib>Dai, Weimin</creatorcontrib><creatorcontrib>Gan, Xiao Dong</creatorcontrib><creatorcontrib>Ali, Sanjida</creatorcontrib><creatorcontrib>Fu, Jennifer</creatorcontrib><creatorcontrib>Back, Stephen A.</creatorcontrib><creatorcontrib>Sanchez, Russell M.</creatorcontrib><creatorcontrib>Segal, Michael M.</creatorcontrib><creatorcontrib>Follett, Pamela L.</creatorcontrib><creatorcontrib>Jensen, Frances E.</creatorcontrib><creatorcontrib>Volpe, Joseph J.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of neuroscience research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosenberg, Paul A.</au><au>Dai, Weimin</au><au>Gan, Xiao Dong</au><au>Ali, Sanjida</au><au>Fu, Jennifer</au><au>Back, Stephen A.</au><au>Sanchez, Russell M.</au><au>Segal, Michael M.</au><au>Follett, Pamela L.</au><au>Jensen, Frances E.</au><au>Volpe, Joseph J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mature myelin basic protein-expressing oligodendrocytes are insensitive to kainate toxicity</atitle><jtitle>Journal of neuroscience research</jtitle><addtitle>J. Neurosci. Res</addtitle><date>2003-01-15</date><risdate>2003</risdate><volume>71</volume><issue>2</issue><spage>237</spage><epage>245</epage><pages>237-245</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>We examined the vulnerability to excitotoxicity of rat oligodendrocytes in dissociated cell culture at different developmental stages. Mature oligodendrocytes that express myelin basic protein were resistant to excitotoxic injury produced by kainate, whereas earlier stages in the oligodendrocyte lineage were vulnerable to this insult. To test the hypothesis that the sensitivity of immature oligodendrocytes and the resistance of mature oligodendrocytes to kainate toxicity were due to differences in membrane responsiveness to kainate, we used whole‐cell patch‐clamp recording. Oligodendrocyte precursors in cultures vulnerable to kainate toxicity responded to 500 μM kainate with large inward currents, whereas mature myelin basic protein‐expressing oligodendrocytes in cultures resistant to kainate toxicity showed no clear response to application of this agonist. We assayed expression of glutamate receptor subunits (GluR) ‐2, ‐4, ‐6, ‐7, and KA2 using immunoblot analysis and found that expression of all of these glutamate receptors was significantly down‐regulated in mature oligodendrocytes. These results suggest a striking developmental regulation of glutamate receptors in oligodendrocytes and suggest that the vulnerability of oligodendrocytes to non‐ N‐methyl‐D‐aspartate receptor‐mediated excitotoxicity might be much greater in developing oligodendrocytes than after the completion of myelination. © 2002 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12503086</pmid><doi>10.1002/jnr.10472</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology Animals Animals, Newborn Cell Culture Techniques Cell Differentiation - drug effects Cell Differentiation - physiology Cell Survival - drug effects cerebral palsy Ciliary Neurotrophic Factor - pharmacology Dose-Response Relationship, Drug Down-Regulation Drug Interactions Electrophysiology - methods Excitatory Amino Acid Agonists - pharmacology Excitatory Amino Acid Antagonists - pharmacology excitotoxicity Fibroblast Growth Factors - pharmacology glutamate hypoxia Immunoblotting Immunohistochemistry ischemia Kainic Acid - pharmacology Myelin Basic Protein - drug effects Myelin Basic Protein - metabolism Oligodendroglia - drug effects Oligodendroglia - metabolism periventricular leukomalacia Platelet-Derived Growth Factor - pharmacology Rats Rats, Sprague-Dawley Receptors, Glutamate - classification Receptors, Glutamate - metabolism |
title | Mature myelin basic protein-expressing oligodendrocytes are insensitive to kainate toxicity |
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