Publikation: Modulation of the Inhibitory Substrate Properties of Oligodendrocytes by Platelet-Derived Growth Factor
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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.
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LANG, 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. 5741-5748BibTex
@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} }
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