p53 in neuronal apoptosis

被引:341
作者
Culmsee, C
Mattson, MP
机构
[1] Univ Munich, Dept Pharm Pharmazeut Biol Biotechnol, Munich, Germany
[2] NIA, Res Program, Neurosci Lab, Baltimore, MD 21224 USA
关键词
p53; MDM-2; BH3-only proteins; DNA damage; glutamate; neurodegeneration;
D O I
10.1016/j.bbrc.2005.03.149
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
The tumor suppressor and transcription factor p53 is a key modulator of cellular stress responses, and activation of p53 can trigger apoptosis in many cell types including neurons. Apoptosis is a form of programmed cell death that occurs in neurons during development of the nervous system and may also be responsible for neuronal deaths that occur in neurological disorders such as stroke, and Alzheimer's and Parkinson's diseases. p53 production is rapidly increased in neurons in response to a range of insults including DNA damage, oxidative stress, metabolic compromise, and cellular calcium overload. Target genes induced by p53 in neurons include those encoding the pro-apoptotic proteins Bax and the BH3-only proteins PUMA and Noxa. In addition to such transcriptional control of the cell death machinery, p53 may more directly trigger apoptosis by acting at the level of mitochondria, a process that can occur in synapses (synaptic apoptosis). Preclinical data suggest that agents that inhibit p53 may be effective therapeutics for several neurodegenerative conditions. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:761 / 777
页数:17
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