Caspase-2: the orphan caspase

被引:87
作者
Bouchier-Hayes, L. [2 ,3 ]
Green, D. R. [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[2] Ctr Cell & Gene Therapy, Houston, TX USA
[3] Baylor Coll Med, Dept Pediat Hematol, Houston, TX 77030 USA
关键词
caspase-2; apoptosis; PIDD; PIDDosome; cell cycle; ACUTE LYMPHOBLASTIC-LEUKEMIA; DOMAIN-CONTAINING PROTEIN; STRESS-INDUCED APOPTOSIS; LEUCINE-RICH REPEAT; KAPPA-B ACTIVATION; DNA-DAMAGE; SUBSTRATE SPECIFICITIES; GENOTOXIC STRESS; DEATH; PIDD;
D O I
10.1038/cdd.2011.157
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
Despite an abundance of literature on the role of caspase-2 in apoptosis, there exists much controversy about this protease making it difficult to place caspase-2 correctly in the apoptotic cascade, and hence its role in apoptosis remains unclear. The identification of the PIDDosome as a signaling platform for caspase-2 activation prompted intense investigation into the true role of this orphan caspase. What has emerged is the idea that caspase-2 may not be mandatory for apoptosis and that activation of this caspase in response to some forms of stress has other effects on the cell such as regulation of cell cycle progression. This idea is particularly relevent to the discovery that caspase-2 may act as a tumor suppressor. Here, we discuss the proposed mechanisms through which caspase-2 signals, in particular those involving PIDD, and their impact on cellular fate. Cell Death and Differentiation (2012) 19, 51-57; doi:10.1038/cdd.2011.157; published online 11 November 2011
引用
收藏
页码:51 / 57
页数:7
相关论文
共 70 条
[1]   The mouse rostral cerebellar malformation gene encodes an UNC-5-like protein [J].
Ackerman, SL ;
Kozak, LP ;
Przyborski, SA ;
Rund, LA ;
Boyer, BB ;
Knowles, BB .
NATURE, 1997, 386 (6627) :838-842
[2]   Restraint of apoptosis during mitosis through interdomain phosphorylation of caspase-2 [J].
Andersen, Joshua L. ;
Johnson, Carrie E. ;
Freel, Christopher D. ;
Parrish, Amanda B. ;
Day, Jennifer L. ;
Buchakjian, Marisa R. ;
Nutt, Leta K. ;
Thompson, J. Will ;
Moseley, M. Arthur ;
Kornbluth, Sally .
EMBO JOURNAL, 2009, 28 (20) :3216-3227
[3]   The domains of death: evolution of the apoptosis machinery [J].
Aravind, L ;
Dixit, VM ;
Koonin, EV .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (02) :47-53
[4]  
Bagatell R, 2004, MOL CANCER THER, V3, P1021
[5]   The biochemical mechanism of caspase-2 activation [J].
Baliga, BC ;
Read, SH ;
Kumar, S .
CELL DEATH AND DIFFERENTIATION, 2004, 11 (11) :1234-1241
[6]   Defects in regulation of apoptosis in caspase-2-deficient mice [J].
Bergeron, L ;
Perez, GI ;
Macdonald, G ;
Shi, LF ;
Sun, Y ;
Jurisicova, A ;
Varmuza, S ;
Latham, KE ;
Flaws, JA ;
Salter, JCM ;
Hara, H ;
Moskowitz, MA ;
Li, E ;
Greenberg, A ;
Tilly, JL ;
Yuan, JY .
GENES & DEVELOPMENT, 1998, 12 (09) :1304-1314
[7]   Apoptosis caused by p53-induced protein with death domain (PIDD) depends on the death adapter protein RAIDD [J].
Berube, C ;
Boucher, LM ;
Ma, W ;
Wakeham, A ;
Salmena, L ;
Hakem, R ;
Yeh, WC ;
Mak, TW ;
Benchimol, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (40) :14314-14319
[8]   Mechanisms of caspase activation [J].
Boatright, KM ;
Salvesen, GS .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (06) :725-731
[9]   A unified model for apical caspase activation [J].
Boatright, KM ;
Renatus, M ;
Scott, FL ;
Sperandio, S ;
Shin, H ;
Pedersen, IM ;
Ricci, JE ;
Edris, WA ;
Sutherlin, DP ;
Green, DR ;
Salvesen, GS .
MOLECULAR CELL, 2003, 11 (02) :529-541
[10]   Caspase-2-induced apoptosis requires bid cleavage: A physiological role for bid in heat shock-induced death [J].
Bonzon, C ;
Bouchier-Hayes, L ;
Pagliari, LJ ;
Green, DR ;
Newmeyer, DD .
MOLECULAR BIOLOGY OF THE CELL, 2006, 17 (05) :2150-2157