Mechanisms of neuronal death in disease: defining the models and the players

被引:82
作者
Ribe, Elena M.
Serrano-Saiz, Esther
Akpan, Nsikan
Troy, Carol M. [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Pathol, Taub Ctr Study Alzheimers Dis & Aging Brain, New York, NY 10032 USA
关键词
Alzheimer's disease; Bcl-2; family; caspase; cerebral ischaemia; inhibitor of apoptosis protein (IAP); stroke;
D O I
10.1042/BJ20081118
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
Dysregulation of life and death at the cellular level leads to a variety of diseases. In the nervous system, aberrant neuronal death is an outstanding feature of neurodegenerative diseases. Since the discovery of the caspase family of proteases, much effort has been made to determine how caspases function in disease, including neurodegenerative diseases. Although many papers have been published examining caspases in neuronal death and disease, the pathways have not been fully clarified. In the present review, we examine the potential players in the death pathways, the current tools for examining these players and the models for studying neurological disease. Alzheimer's disease, the most common neurodegenerative disorder, and cerebral ischaemia, the most common cause of neurological death, are used to illustrate our current understanding of death signalling in neurodegenerative diseases. A better understanding of the neuronal death pathways would provide targets for the development of therapeutic interventions for these diseases.
引用
收藏
页码:165 / 182
页数:18
相关论文
共 202 条
[31]   GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES [J].
CORDER, EH ;
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, DE ;
GASKELL, PC ;
SMALL, GW ;
ROSES, AD ;
HAINES, JL ;
PERICAKVANCE, MA .
SCIENCE, 1993, 261 (5123) :921-923
[32]   A POTENTIAL ROLE FOR APOPTOSIS IN NEURODEGENERATION AND ALZHEIMERS-DISEASE [J].
COTMAN, CW ;
ANDERSON, AJ .
MOLECULAR NEUROBIOLOGY, 1995, 10 (01) :19-45
[33]   p53-induced protein with a death domain (PIDD) isoforms differentially activate nuclear factor-kappaB and caspase-2 in response to genotoxic stress [J].
Cuenin, S. ;
Tinel, A. ;
Janssens, S. ;
Tschopp, J. .
ONCOGENE, 2008, 27 (03) :387-396
[34]   EXPRESSION OF THE ALZHEIMER AMYLOID-PROMOTING FACTOR ANTICHYMOTRYPSIN IS INDUCED IN HUMAN ASTROCYTES BY IL-1 [J].
DAS, S ;
POTTER, H .
NEURON, 1995, 14 (02) :447-456
[35]   Highly efficient small interfering RNA delivery to primary mammalian neurons induces MicroRNA-like effects before mRNA degradation [J].
Davidson, TJ ;
Harel, S ;
Arboleda, VA ;
Prunell, GF ;
Shelanski, ML ;
Greene, LA ;
Troy, CM .
JOURNAL OF NEUROSCIENCE, 2004, 24 (45) :10040-10046
[36]   Pathogenic APP mutations near the γ-secretase cleavage site differentially affect Aβ secretion and APP C-terminal fragment stability [J].
De Jonghe, C ;
Esselens, C ;
Kumar-Singh, S ;
Craessaerts, K ;
Serneels, S ;
Checler, F ;
Annaert, W ;
Van Broeckhoven, C ;
De Strooper, B .
HUMAN MOLECULAR GENETICS, 2001, 10 (16) :1665-1671
[37]   Focus on research - Stroke and neurovascular protection [J].
del Zoppo, GJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (06) :553-555
[38]   Caspase 3 attenuates XIAP (X-linked inhibitor of apoptosis protein)-mediated inhibition of caspase 9 [J].
Denault, Jean-Bernard ;
Eckelman, Brendan P. ;
Shin, Hwain ;
Pop, Cristina ;
Salvesen, Guy S. .
BIOCHEMICAL JOURNAL, 2007, 405 :11-19
[39]  
DRONNE MA, 2008, PROG BIOPHYS MOL BIO, V97, P28
[40]   Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition [J].
Du, CY ;
Fang, M ;
Li, YC ;
Li, L ;
Wang, XD .
CELL, 2000, 102 (01) :33-42