Neuronal caspase-3 signaling: not only cell death

被引:390
|
作者
D'Amelio, M. [1 ,2 ]
Cavallucci, V. [1 ,2 ]
Cecconi, F. [1 ,2 ]
机构
[1] IRCCS Fdn Santa Lucia, Lab Mol Neuroembryol, I-00143 Rome, Italy
[2] Univ Roma Tor Vergata, Dept Biol, Dulbecco Telethon Inst, I-00173 Rome, Italy
关键词
apoptosis; neurodevelopment; neuron differentiation; synaptic plasticity; neurodegeneration; AMYOTROPHIC-LATERAL-SCLEROSIS; TRANSGENIC MOUSE MODEL; ISCHEMIC BRAIN-INJURY; ALZHEIMERS-DISEASE; PARKINSONS-DISEASE; CYTOCHROME-C; HUNTINGTONS-DISEASE; DIFFERENTIAL REQUIREMENT; DOPAMINERGIC-NEURONS; SYNAPTIC PLASTICITY;
D O I
10.1038/cdd.2009.180
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
Caspases are a family of cysteinyl aspartate-specific proteases that are highly conserved in multicellular organisms and function as central regulators of apoptosis. A member of this family, caspase-3, has been identified as a key mediator of apoptosis in neuronal cells. Recent studies in snail, fly and rat suggest that caspase-3 also functions as a regulatory molecule in neurogenesis and synaptic activity. In this study, in addition to providing an overview of the mechanism of caspase-3 activation, we review genetic and pharmacological studies of apoptotic and nonapoptotic functions of caspase-3 and discuss the regulatory mechanism of caspase-3 for executing nonapoptotic functions in the central nervous system. Knowledge of biochemical pathway(s) for nonapoptotic activation and modulation of caspase-3 has potential implications for the understanding of synaptic failure in the pathophysiology of neurological disorders. Fine-tuning of caspase-3 lays down a new challenge in identifying pharmacological avenues for treatment of many neurological disorders. Cell Death and Differentiation (2010) 17, 1104-1114; doi:10.1038/cdd.2009.180; published online 4 December 2009
引用
收藏
页码:1104 / 1114
页数:11
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