DNA damage- and stress-induced apoptosis occurs independently of PIDD

被引:41
作者
Kim, Ira R. [1 ,2 ]
Murakami, Kiichi [1 ,3 ]
Chen, Nien-Jung [1 ]
Saibil, Samuel D. [1 ,3 ]
Matysiak-Zablocki, Elzbieta [1 ]
Elford, Alisha R. [1 ]
Bonnard, Madeleine [3 ]
Benchimol, Samuel [4 ]
Jurisicova, Andrea [5 ]
Yeh, Wen-Chen [1 ,2 ]
Ohashi, Pamela S. [1 ,2 ,3 ]
机构
[1] Univ Hlth Network, Ontario Canc Inst, Campbell Family Inst, Toronto, ON M5G 2C1, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON, Canada
[4] York Univ, Dept Biol, Toronto, ON M3J 2R7, Canada
[5] Univ Toronto, Samuel Lunenfeld Res Inst, Dept Obstet & Gynecol, MSH, Toronto, ON M5T 3H7, Canada
关键词
PIDD; Caspase-2; p53; Apoptosis; Gene-targeting; CELL-DEATH; LYMPHOPROLIFERATIVE SYNDROME; P53-INDUCED PROTEIN; GENOTOXIC STRESS; CASPASE-2; P53; ACTIVATION; PIDDOSOME; COMPLEX; CHECKPOINT;
D O I
10.1007/s10495-009-0375-1
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 p53-induced protein with a death domain, PIDD, was identified as a p53 target gene whose main role is to execute apoptosis in a p53-dependent manner. To investigate the physiological role of PIDD in apoptosis, we generated PIDD-deficient mice. Here, we report that, although PIDD expression is inducible upon DNA damage, PIDD-deficient mice undergo apoptosis normally not only in response to DNA damage, but also in response to various p53-independent stress signals and to death receptor (DR) engagement. This indicates that PIDD is not required for DNA damage-, stress-, and DR-induced apoptosis. Also, in the absence of PIDD, both caspase-2 processing and activation occur in response to DNA damage. Our findings demonstrate that PIDD does not play an essential role for all p53-mediated or p53-independent apoptotic pathways.
引用
收藏
页码:1039 / 1049
页数:11
相关论文
共 31 条
[1]   Ways of dying: multiple pathways to apoptosis [J].
Adams, JM .
GENES & DEVELOPMENT, 2003, 17 (20) :2481-2495
[2]   Targeting death and decoy receptors of the tumour-necrosis factor superfamily [J].
Ashkenazi, A .
NATURE REVIEWS CANCER, 2002, 2 (06) :420-430
[3]   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
[4]   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
[5]   Genetic disorders of programmed cell death in the immune system [J].
Bidere, Nicolas ;
Su, Helen C. ;
Lenardo, Michael J. .
ANNUAL REVIEW OF IMMUNOLOGY, 2006, 24 :321-352
[6]   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
[7]   DOMINANT INTERFERING FAS GENE-MUTATIONS IMPAIR APOPTOSIS IN A HUMAN AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME [J].
FISHER, GH ;
ROSENBERG, FJ ;
STRAUS, SE ;
DALE, JK ;
MIDDELTON, LA ;
LIN, AY ;
STROBER, W ;
LENARDO, MJ ;
PUCK, JM .
CELL, 1995, 81 (06) :935-946
[8]   Caspase-2 is required for cell death induced by cytoskeletal disruption [J].
Ho, L. H. ;
Read, S. H. ;
Dorstyn, L. ;
Lambrusco, L. ;
Kumar, S. .
ONCOGENE, 2008, 27 (24) :3393-3404
[9]   PIDD mediates NF-κB activation in response to DNA damage [J].
Janssens, S ;
Tinel, A ;
Lippens, S ;
Tschopp, J .
CELL, 2005, 123 (06) :1079-1092
[10]   AMP-activated protein kinase induces a p53-dependent metabolic checkpoint [J].
Jones, RG ;
Plas, DR ;
Kubek, S ;
Buzzai, M ;
Mu, J ;
Xu, Y ;
Birnbaum, MJ ;
Thompson, CB .
MOLECULAR CELL, 2005, 18 (03) :283-293