| Literature DB >> 15592360 |
H Kadowaki1, H Nishitoh, F Urano, C Sadamitsu, A Matsuzawa, K Takeda, H Masutani, J Yodoi, Y Urano, T Nagano, H Ichijo.
Abstract
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.Entities:
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Year: 2005 PMID: 15592360 DOI: 10.1038/sj.cdd.4401528
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828