Modulation of the Inhibitory Substrate Properties of Oligodendrocytes by Platelet-Derived Growth Factor

dc.contributor.authorLang, Dirk M.deu
dc.contributor.authorHille, Michaeldeu
dc.contributor.authorSchwab, Martin E.deu
dc.contributor.authorStürmer, Claudia
dc.date.accessioned2011-03-24T17:41:11Zdeu
dc.date.available2011-03-24T17:41:11Zdeu
dc.date.issued1996deu
dc.description.abstractAlthough growth cones typically collapse after encountering O1/galactocerebroside (GalC)-positive oligodendrocytes, the majority of growth cones traversed oligodendrocytes, which were raised for 8-10 d in medium containing 10 ng/ml platelet-derived growth factor (PDGF). Oligodendrocytes raised 8-10 d in control medium caused growth cone collapse as they normally do, but failed to elicit this response after being transferred to PDGF-containing medium for an additional 8-10 d. The opposite was observed when PDGF-treated oligodendrocytes were brought to control medium. Growth cones collapsed when contacting these cells. Oligodendrocytes also lost their collapse-inducing activity when raised in medium conditioned by astrocytes, known to produce PDGF. Antibody IN-1 is directed against neurite growth inhibitors (NI), proteins of 35 and 250 kDa on the surface of O1/GalC-positive oligodendrocytes, which are known to elicit growth cone collapse. IN-1 immunoreactivity was markedly reduced in PDGF-treated oligodendrocytes. However, both PDGF-treated and control oligodendrocytes exhibited myelin-associated glycoprotein, proteolipid protein, and myelin basic protein immunoreactivity. This suggests that PDGF-treatment affects NI expression but does not interfere with the expression of advanced myelin marker proteins. Because NI cause growth cone collapse, the loss of collapse-inducing activity by PDGF-treated oligodendrocytes suggests that PDGF regulates, directly or indirectly, the expression of these proteins.eng
dc.description.versionpublished
dc.format.mimetypeapplication/pdfdeu
dc.identifier.citationFirst publ. in: The Journal of Neuroscience 16 (1996), 18, pp. 5741-5748deu
dc.identifier.ppn274694395deu
dc.identifier.urihttp://kops.uni-konstanz.de/handle/123456789/8178
dc.language.isoengdeu
dc.legacy.dateIssued2007deu
dc.rightsAttribution-NonCommercial-NoDerivs 2.0 Generic
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/
dc.subjectoligodendrocytedeu
dc.subjectloss of inhibitory propertiesdeu
dc.subjectPDGF-treatmentdeu
dc.subjectgrowth cone collapsedeu
dc.subjectIN-1 immunoreactivitydeu
dc.subjectastrocyte-conditioned mediumdeu
dc.subject.ddc570deu
dc.titleModulation of the Inhibitory Substrate Properties of Oligodendrocytes by Platelet-Derived Growth Factoreng
dc.typeJOURNAL_ARTICLEdeu
dspace.entity.typePublication
kops.citation.bibtex
@article{Lang1996Modul-8178,
  year={1996},
  title={Modulation of the Inhibitory Substrate Properties of Oligodendrocytes by Platelet-Derived Growth Factor},
  number={18},
  volume={16},
  journal={The Journal of Neuroscience},
  pages={5741--5748},
  author={Lang, Dirk M. and Hille, Michael and Schwab, Martin E. and Stürmer, Claudia}
}
kops.citation.iso690LANG, Dirk M., Michael HILLE, Martin E. SCHWAB, Claudia STÜRMER, 1996. Modulation of the Inhibitory Substrate Properties of Oligodendrocytes by Platelet-Derived Growth Factor. In: The Journal of Neuroscience. 1996, 16(18), pp. 5741-5748deu
kops.citation.iso690LANG, Dirk M., Michael HILLE, Martin E. SCHWAB, Claudia STÜRMER, 1996. Modulation of the Inhibitory Substrate Properties of Oligodendrocytes by Platelet-Derived Growth Factor. In: The Journal of Neuroscience. 1996, 16(18), pp. 5741-5748eng
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    <dcterms:abstract xml:lang="eng">Although growth cones typically collapse after encountering O1/galactocerebroside (GalC)-positive oligodendrocytes, the majority of growth cones traversed oligodendrocytes, which were raised for 8-10 d in medium containing 10 ng/ml platelet-derived growth factor (PDGF). Oligodendrocytes raised 8-10 d in control medium caused growth cone collapse as they normally do, but failed to elicit this response after being transferred to PDGF-containing medium for an additional 8-10 d. The opposite was observed when PDGF-treated oligodendrocytes were brought to control medium. Growth cones collapsed when contacting these cells. Oligodendrocytes also lost their collapse-inducing activity when raised in medium conditioned by astrocytes, known to produce PDGF. Antibody IN-1 is directed against neurite growth inhibitors (NI), proteins of 35 and 250 kDa on the surface of O1/GalC-positive oligodendrocytes, which are known to elicit growth cone collapse. IN-1 immunoreactivity was markedly reduced in PDGF-treated oligodendrocytes. However, both PDGF-treated and control oligodendrocytes exhibited myelin-associated glycoprotein, proteolipid protein, and myelin basic protein immunoreactivity. This suggests that PDGF-treatment affects NI expression but does not interfere with the expression of advanced myelin marker proteins. Because NI cause growth cone collapse, the loss of collapse-inducing activity by PDGF-treated oligodendrocytes suggests that PDGF regulates, directly or indirectly, the expression of these proteins.</dcterms:abstract>
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kops.sourcefieldThe Journal of Neuroscience. 1996, <b>16</b>(18), pp. 5741-5748deu
kops.sourcefield.plainThe Journal of Neuroscience. 1996, 16(18), pp. 5741-5748deu
kops.sourcefield.plainThe Journal of Neuroscience. 1996, 16(18), pp. 5741-5748eng
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source.periodicalTitleThe Journal of Neuroscience

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