Amyloid beta induces neuronal cell death through ROS-mediated ASK1 activation
Kadowaki, H. ; Nishitoh, H. ; Urano, Fumihiko ; Sadamitsu, C. ; Matsuzawa, A. ; Takeda, K. ; Masutani, H. ; Yodoi, J. ; Urano, Y. ; Nagano, T. ... show 1 more
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Student Authors
Faculty Advisor
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UMass Chan Affiliations
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Keywords
Amyloid beta-Peptides
Animals
Cell Death
Endoplasmic Reticulum
Enzyme Activation
JNK Mitogen-Activated Protein Kinases
MAP Kinase Kinase Kinase 5
Membrane Proteins
Mice
Mice, Inbred C57BL
Mice, Knockout
Neurons
Nitrogen Oxides
PC12 Cells
Peptide Fragments
Protein-Serine-Threonine Kinases
Rats
Reactive Oxygen Species
eIF-2 Kinase
Genetics and Genomics
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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.
Source
Cell Death Differ. 2005 Jan;12(1):19-24. Link to article on publisher's site