Amyloid β induces neuronal cell death through ROS-mediated ASK1 activation

被引:359
作者
Kadowaki, H
Nishitoh, H
Urano, F
Sadamitsu, C
Matsuzawa, A
Takeda, K
Masutani, H
Yodoi, J
Urano, Y
Nagano, T
Ichijo, H
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Cell Signaling, Bunkyo Ku, Tokyo 1130033, Japan
[2] Japan Sci & Technol Corp, CREST, Bunkyo Ku, Tokyo 1130033, Japan
[3] Tokyo Med & Dent Univ, Grad Sch, Lab Cell Signaling, Bunkyo Ku, Tokyo 1138549, Japan
[4] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01605 USA
[5] Univ Tokyo, Grad Sch Pharmaceut Sci, Ctr Excellence Program, Bunkyo Ku, Tokyo 1130033, Japan
[6] Kyoto Univ, Inst Virus Res, Dept Biol Responses, Kyoto 6068507, Japan
[7] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Chem & Biol, Bunkyo Ku, Tokyo 1130033, Japan
关键词
amyloid beta; ASK1; JNK; reactive oxygen species (ROS); neuronal cell death;
D O I
10.1038/sj.cdd.4401528
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Amyloid beta (Abeta) is a main component of senile plaques in Alzheimer's disease and induces neuronal cell death. Reactive oxygen species (ROS), nitric oxide and endoplasmic reticulum (ER) stress have been implicated in Abeta-induced neurotoxicity. We have reported that apoptosis signal-regulating kinase 1 (ASK1) is required for ROS- and ER stress-induced JNK activation and apoptosis. Here we show the involvement of ASK1 in Abeta-induced neuronal cell death. Abeta activated ASK1 mainly through production of ROS but not through ER stress in cultured neuronal cells. Importantly, ASK1(-/-) neurons were defective in Abeta-induced JNK activation and cell death. These results indicate that ROS- mediated ASK1 activation is a key mechanism for Abeta-induced neurotoxicity, which plays a central role in Alzheimer's disease.
引用
收藏
页码:19 / 24
页数:6
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