Apoptosis Signal Regulating Kinase 1 ( ASK1): Potential as a Therapeutic Target for Alzheimer's Disease

被引:62
作者
Song, Juhyun [1 ]
Park, Kyung Ah [1 ]
Lee, Won Taek [1 ]
Lee, Jong Eun [1 ,2 ]
机构
[1] Yonsei Univ, Coll Med, Dept Anat, Seoul 120752, South Korea
[2] Yonsei Univ, Coll Med, Plus Project Med Sci BK21, Seoul 120752, South Korea
基金
新加坡国家研究基金会;
关键词
apoptosis signal regulating kinase 1 (ASK1); Alzheimer's disease (AD); oxidative stress; endoplasmic reticulum (ER) stress; A neurotoxicity; tau protein phosphorylation; insulin signal transduction; ENDOPLASMIC-RETICULUM STRESS; INSULIN-RECEPTOR SUBSTRATE-1; CENTRAL-NERVOUS-SYSTEM; NEURONAL CELL-DEATH; N-TERMINAL KINASE; INCREASED VULNERABILITY; SYNAPTIC PLASTICITY; TAU PHOSPHORYLATION; HIPPOCAMPAL-NEURONS; GABA(A) RECEPTORS;
D O I
10.3390/ijms15022119
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
Alzheimer's disease (AD) is the most common form of dementia, characterized by a decline in memory and cognitive function. Clinical manifestations of AD are closely associated with the formation of senile plaques and neurofibrillary tangles, neuronal loss and cognitive decline. Apoptosis signal regulating kinase 1 (ASK1) is a mediator of the MAPK pathway, which regulates various cellular responses such as apoptosis, cell survival, and differentiation. Accumulating evidence indicates that ASK1 plays a key role in the pathogenesis of neurodegenerative disorders such as Huntington's disease and AD. Of particular interest, ASK1 is associated with many signaling pathways, which include endoplasmic reticulum (ER) stress-mediated apoptosis, A-induced neurotoxicity, tau protein phosphorylation, and insulin signal transduction. Here, we review experimental evidence that links ASK1 signaling and AD pathogenesis and propose that ASK1 might be a new point of therapeutic intervention to prevent or treat AD.
引用
收藏
页码:2119 / 2129
页数:11
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