Expansion and evolution of cell death programmes

被引:435
作者
Degterev, Alexei [2 ]
Yuan, Junying [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[2] Tufts Univ, Sch Med, Dept Biochem, Boston, MA 02111 USA
关键词
D O I
10.1038/nrm2393
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cell death has historically been subdivided into regulated and unregulated mechanisms. Apoptosis, a form of regulated cell death, reflects a cell's decision to die in response to cues and is executed by intrinsic cellular machinery. Unregulated cell death (often called necrosis) is caused by overwhelming stress that is incompatible with cell survival. Emerging evidence, however, suggests that these two processes do not adequately explain the various cell death mechanisms. Recent data point to the existence of multiple non-apoptotic, regulated cell death mechanisms, some of which overlap or are mutually exclusive with apoptosis. Here we examine how and why these different cell death programmes have evolved, with an eye towards new cytoprotective therapeutic opportunities.
引用
收藏
页码:378 / 390
页数:13
相关论文
共 144 条
[1]   Programmed cell death mediated by ced-3 and ced-4 protects Caenorhabditis elegans from Salmonella typhimurium-mediated killing [J].
Aballay, A ;
Ausubel, FM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (05) :2735-2739
[2]   A morphologically conserved nonapoptotic program promotes linker cell death in Caenorhabditis elegans [J].
Abraham, Mary C. ;
Lu, Yun ;
Shaham, Shai .
DEVELOPMENTAL CELL, 2007, 12 (01) :73-86
[3]   Three-dimensional structure of the apoptosome: Implications for assembly, procaspase-9 binding, and activation [J].
Acehan, D ;
Jiang, XJ ;
Morgan, DG ;
Heuser, JE ;
Wang, XD ;
Akey, CW .
MOLECULAR CELL, 2002, 9 (02) :423-432
[4]  
de la Lastra CA, 2007, CURR PHARM DESIGN, V13, P933
[5]   Autophagy inhibition enhances therapy-induced apoptosis in a Myc-induced model of lymphoma [J].
Amaravadi, Ravi K. ;
Yu, Duonan ;
Lum, Julian J. ;
Bui, Thi ;
Christophorou, Maria A. ;
Evan, Gerard I. ;
Thomas-Tikhonenko, Andrei ;
Thompson, Craig B. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (02) :326-336
[6]   The PARP superfamily [J].
Amé, JC ;
Spenlehauer, C ;
de Murcia, G .
BIOESSAYS, 2004, 26 (08) :882-893
[7]   Poly(ADP-ribose) (PAR) polymer is a death signal [J].
Andrabi, Shaida A. ;
Kim, No Soo ;
Yu, Seong-Woon ;
Wang, Hongmin ;
Koh, David W. ;
Sasaki, Masayuki ;
Klaus, Judith A. ;
Otsuka, Takashi ;
Zhang, Zhizheng ;
Koehler, Raymond C. ;
Hurn, Patricia D. ;
Poirier, Guy G. ;
Dawson, Valina L. ;
Dawson, Ted M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (48) :18308-18313
[8]   A FADD-dependent innate immune mechanism in mammalian cells [J].
Balachandran, S ;
Thomas, E ;
Barber, GN .
NATURE, 2004, 432 (7015) :401-405
[9]   The CD95 type I/type II model [J].
Barnhart, BC ;
Alappat, EC ;
Peter, ME .
SEMINARS IN IMMUNOLOGY, 2003, 15 (03) :185-193
[10]   Growth arrest and autophagy are required for salivary gland cell degradation in Drosophila [J].
Berry, Deborah L. ;
Baehrecke, Eric H. .
CELL, 2007, 131 (06) :1137-1148