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
相关论文
共 90 条
[1]   The two Drosophila cytochrome C proteins can function in both respiration and caspase activation [J].
Arama, E ;
Bader, M ;
Srivastava, M ;
Bergmann, A ;
Steller, H .
EMBO JOURNAL, 2006, 25 (01) :232-243
[2]   Caspase activity and a specific cytochrome c are required for sperm differentiation in Drosophila [J].
Arama, E ;
Agapite, J ;
Steller, H .
DEVELOPMENTAL CELL, 2003, 4 (05) :687-697
[3]  
Arama E, 2007, PLOS BIOL, V5, P2745, DOI 10.1371/journal.pbio.0050251
[4]   Glial pathology but absence of apoptotic nigral neurons in long-standing Parkinson's disease [J].
Banati, RB ;
Daniel, SE ;
Blunt, SB .
MOVEMENT DISORDERS, 1998, 13 (02) :221-227
[5]   Caspase-like activity is essential for long-term synaptic plasticity in the terrestrial snail Helix [J].
Bravarenko, NI ;
Onufriev, MV ;
Stepanichev, MY ;
Ierusalimsky, VN ;
Balaban, PM ;
Gulyaeva, NV .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2006, 23 (01) :129-140
[6]   Caspase-mediated cleavage is not required for the activity of presenilins in amyloidogenesis and NOTCH signaling [J].
Brockhaus, M ;
Grünberg, J ;
Röhrig, S ;
Loetscher, H ;
Wittenburg, N ;
Baumeister, R ;
Jacobsen, H ;
Haass, C .
NEUROREPORT, 1998, 9 (07) :1481-1486
[7]   Nuclear factor TDP-43 binds to the polymorphic TG repeats in CFTR intron 8 and causes skipping of Exon 9: A functional link with disease penetrance [J].
Buratti, E ;
Brindisi, A ;
Pagani, F ;
Baralle, FE .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (06) :1322-1325
[8]  
Burek MJ, 1999, CELL DEATH AND DISEASES OF THE NERVOUS SYSTEM, P145
[9]   The involvement of cell death and survival in neural tube defects: a distinct role for apoptosis and autophagy? [J].
Cecconi, F. ;
Piacentini, M. ;
Fimia, G. M. .
CELL DEATH AND DIFFERENTIATION, 2008, 15 (07) :1170-1177
[10]   Apaf1 (CED-4 homolog) regulates programmed cell death in mammalian development [J].
Cecconi, F ;
Alvarez-Bolado, G ;
Meyer, BI ;
Roth, KA ;
Gruss, P .
CELL, 1998, 94 (06) :727-737