GAPDH knockdown rescues mesencephalic dopaminergic neurons from MPP+-induced apoptosis

被引:45
作者
Fukuhara, Y
Takeshima, T
Kashiwaya, Y
Shimoda, K
Ishitani, R
Nakashima, K
机构
[1] Tottori Univ, Fac Med, Inst Neurol Sci, Div Neurol, Yonago, Tottori 6838504, Japan
[2] Josai Univ, Grp Cellular Neurobiol, Sakado, Saitama 3500248, Japan
[3] Natl Nishitottori Hosp, Tottori 6890203, Japan
关键词
apoptosis; glyceraldehyde-3-phosphate dehydrogenase; microisland culture; MPTP; nuclear accumulation;
D O I
10.1097/00001756-200107030-00051
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glyceraldehyde-3-phosphate dehydrogenase (GAPDH; EC 1.2.1.12) has a number of diverse functions apart from glycolytic function. We explored the possible involvement of GAPDH in 1-methyl-4-phenylpyridinium (MPP+)-induced death of mesencephalic dopaminergic neurons (MDNs) in culture, MPP+ (10 and 20 muM, 24 h) exposure selectively decreased the survival of tyrosine hydroxylase positive (TH+) MDNs, which manifested apoptotic features including shrinkage of the fell body, chromatin condensation and nuclear fragmentation. Two types of GAPDH antisense oligonucleotides almost completely rescued MDNs from MPP+ toxicity. GAPDH was strongly expressed in apoptotic TH+ neurons, and MPP+ exposure significantly increased the percentage of TH+ neurons in which GAPDH is over-expressed. Confocal microscopic analysis demonstrated the nuclear accumulation of GAPDH in neurons undergoing MPP+-induced apoptosis. These results suggest that MPP+ causes apoptosis of MDNs, concomitant with the overexpression and nuclear accumulation of GAPDH. NeuroReport 12:2049-2052 (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:2049 / 2052
页数:4
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