Mature myelin basic protein-expressing oligodendrocytes kainate toxicity

被引:108
作者
Rosenberg, PA
Dai, WM
Gan, XD
Ali, S
Fu, J
Back, SA
Sanchez, RM
Segal, MM
Follett, PL
Jensen, FE
Volpe, JJ
机构
[1] Childrens Hosp, Dept Neurol, Boston, MA 02115 USA
[2] Childrens Hosp, Program Neurosci, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
excitotoxicity; glutamate; periventricular leukomalacia; cerebral palsy; hypoxia; ischemia;
D O I
10.1002/jnr.10472
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 muM 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 nonN-methyl-D-aspartate receptor-mediated excitotoxicity might be much greater in developing oligodendrocytes than after the completion of myelination. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:237 / 245
页数:9
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