Multiple classes of the oligodendrocyte lineage are highly vulnerable to excitotoxicity

被引:82
作者
McDonald, JW
Levine, JM
Qu, Y
机构
[1] Washington Univ, Sch Med, Ctr Study Nervous Syst Injury, St Louis, MO 63110 USA
[2] SUNY Stony Brook, Dept Neurobiol & Behav, Stony Brook, NY 11794 USA
[3] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
关键词
cell culture; excitatory amino acid receptors; excitotoxicity; Gal-C (galactocerebroside); glutamate; kainate; myelination; MBP (myelin basic protein); NG2; O2-A progenitors; oligodendrocytes;
D O I
10.1097/00001756-199808240-00014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
WE have recently shown that galactocerebroside (Gal-C)-expressing oligodendrocytes are highly vulnerable to (AMPA)/kainate receptor-mediated death. Here we examined the vulnerability of cells at different developmental stages of the oligodendrocyte lineage to AMPA/kainate receptor-mediated excitotoxicity. Oligodendrocyte precursor cells, pre-oligodendrocytes and mature oligodendrocytes were killed by 24 h exposures to low concentrations of kainate (30-100 mu M) Death was attenuated by the AMPA/kainate receptor antagonist 6-nitro-7-sulfamoylbenzo (f) quinoxaline-2,3-dione (NBQX). The high vulnerability of oligodendrocytes and their precursors to AMPA/kainate receptor excitotoxicity may represent an important mechanism of white matter damage resulting from trauma or ischemia in the perinatal and adult central nervous system (CNS). (C) 1998 Lippincott Williams & Wilkins.
引用
收藏
页码:2757 / 2762
页数:6
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