SMI-32 ANTIBODY AGAINST NONPHOSPHORYLATED NEUROFILAMENTS IDENTIFIES A SUBPOPULATION OF CULTURED CORTICAL-NEURONS HYPERSENSITIVE TO KAINATE TOXICITY

被引:16
作者
GOTTRON, F
TURETSKY, D
CHOI, D
机构
[1] WASHINGTON UNIV, SCH MED, DEPT NEUROL, ST LOUIS, MO 63110 USA
[2] WASHINGTON UNIV, SCH MED, CTR STUDY NERVOUS SYST INJURY, ST LOUIS, MO 63110 USA
关键词
ALZHEIMERS DISEASE; HUNTINGTONS DISEASE; SELECTIVE VULNERABILITY; NEUROFILAMENTS; IMMUNOCYTOCHEMISTRY;
D O I
10.1016/0304-3940(95)11698-V
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
SMI-32, an antibody against a non-phosphorylated neurofilament epitope identifies a subpopulation of human cortical neurons preferentially lost in Alzheimer's or Huntington's disease. In murine cortical cultures SMI-32 labeled a small subset of neurons exhibiting enhanced vulnerability to kainate toxicity. Most SMI 32(+) neurons were GABAergic and exhibited kainate-activated Co2+ uptake. Thus expression of Ca2+ permeable AMPA or kainate receptor-gated channels likely underlies the heightened vulnerability of SMI-32(+) cortical neurons to kainate.
引用
收藏
页码:1 / 4
页数:4
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