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
Hauptverfasser: 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.
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container_end_page 245
container_issue 2
container_start_page 237
container_title Journal of neuroscience research
container_volume 71
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.
doi_str_mv 10.1002/jnr.10472
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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. 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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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source Wiley-Blackwell Journals; MEDLINE
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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