Molecular mechanisms of necroptosis: an ordered cellular explosion

被引:1854
作者
Vandenabeele, Peter [1 ,2 ]
Galluzzi, Lorenzo [3 ,4 ,5 ]
Vanden Berghe, Tom [1 ,2 ]
Kroemer, Guido [3 ,4 ,6 ,7 ,8 ]
机构
[1] Univ Ghent VIB, Mol Signalling & Cell Death Unit, Dept Mol Biomed Res, B-9052 Ghent, Belgium
[2] Univ Ghent VIB, Dept Biomed Mol Biol, B-9052 Ghent, Belgium
[3] INSERM, U848, F-94805 Villejuif, France
[4] Inst Gustave Roussy, F-94805 Villejuif, France
[5] Univ Paris 11, F-94805 Villejuif, France
[6] Ctr Rech Cordoliers, F-75005 Paris, France
[7] Pole Biol Hop Europeen Georges Pompidou, AP HP, F-75908 Paris, France
[8] Univ Paris 05, F-75270 Paris, France
关键词
TUMOR-NECROSIS-FACTOR; NF-KAPPA-B; RECEPTOR-INTERACTING PROTEIN; MITOCHONDRIAL PERMEABILITY TRANSITION; APOPTOSIS-INDUCING FACTOR; LYSOSOMAL MEMBRANE PERMEABILIZATION; MEDIATED PROGRAMMED NECROSIS; FOCAL CEREBRAL-ISCHEMIA; DEATH DOMAIN KINASE; OXIDATIVE STRESS;
D O I
10.1038/nrm2970
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
For a long time, apoptosis was considered the sole form of programmed cell death during development, homeostasis and disease, whereas necrosis was regarded as an unregulated and uncontrollable process. Evidence now reveals that necrosis can also occur in a regulated manner. The initiation of programmed necrosis, 'necroptosis', by death receptors (such as tumour necrosis factor receptor 1) requires the kinase activity of receptor-interacting protein 1 (RIP1; also known as RIPK1) and RIP3 (also known as RIPK3), and its execution involves the active disintegration of mitochondrial, lysosomal and plasma membranes. Necroptosis participates in the pathogenesis of diseases, including ischaemic injury, neurodegeneration and viral infection, thereby representing an attractive target for the avoidance of unwarranted cell death.
引用
收藏
页码:700 / 714
页数:15
相关论文
共 171 条
[91]   PROGRAMMED CELL DEATH .2. ENDOCRINE POTENTIATION OF THE BREAKDOWN OF THE INTERSEGMENTAL MUSCLES OF SILKMOTHS [J].
LOCKSHIN, RA ;
WILLIAMS, CM .
JOURNAL OF INSECT PHYSIOLOGY, 1964, 10 (04) :643-649
[92]   Activation and caspase-mediated inhibition of PARP: A molecular switch between fibroblast necrosis and apoptosis in death receptor signaling [J].
Los, M ;
Mozoluk, M ;
Ferrari, D ;
Stepczynska, A ;
Stroh, C ;
Renz, A ;
Herceg, Z ;
Wang, ZQ ;
Schulze-Osthoff, K .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (03) :978-988
[93]   Inhibition of tumor necrosis factor-induced cell death in MCF7 by a novel inhibitor of neutral sphingomyelinase [J].
Luberto, C ;
Hassler, DF ;
Signorelli, P ;
Okamoto, Y ;
Sawai, H ;
Boros, E ;
Hazen-Martin, DJ ;
Obeid, LM ;
Hannun, YA ;
Smith, GK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (43) :41128-41139
[94]   NF-κB protects macrophages from lipopolysaccharide-induced cell death -: The role of caspase 8 and receptor-interacting protein [J].
Ma, YY ;
Temkin, V ;
Liu, HT ;
Pope, RM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (51) :41827-41834
[95]   Inhibition of proinflarnmatory and innate immune signaling pathways by a cytomegalovirus RIP1-interacting protein [J].
Mack, Claudia ;
Sickmann, Albert ;
Lembo, David ;
Brune, Wolfram .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (08) :3094-3099
[96]   EARLY REDISTRIBUTION OF PLASMA-MEMBRANE PHOSPHATIDYLSERINE IS A GENERAL FEATURE OF APOPTOSIS REGARDLESS OF THE INITIATING STIMULUS - INHIBITION BY OVEREXPRESSION OF BCL-2 AND ABL [J].
MARTIN, SJ ;
REUTELINGSPERGER, CPM ;
MCGAHON, AJ ;
RADER, JA ;
VANSCHIE, RCAA ;
LAFACE, DM ;
GREEN, DR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (05) :1545-1556
[97]   NALP Inflammasomes:: A central role in innate immunity [J].
Martinon, Fabio ;
Gaide, Olivier ;
Petrilli, Virgine ;
Mayor, Annick ;
Tschopp, Juerg .
SEMINARS IN IMMUNOPATHOLOGY, 2007, 29 (03) :213-229
[98]   Cyld inhibits tumor cell proliferation by blocking Bcl-3-dependent NF-κB signaling [J].
Massoumi, Ramin ;
Chmielarska, Katarzyna ;
Hennecke, Katharina ;
Pfeifer, Alexander ;
Faessler, Reinhard .
CELL, 2006, 125 (04) :665-677
[99]   Glutamine homeostasis and mitochondrial dynamics [J].
Mates, Jose M. ;
Segura, Juan A. ;
Campos-Sandoval, Jose A. ;
Lobo, Carolina ;
Alonso, Lorenzo ;
Alonso, Francisco J. ;
Marquez, Javier .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2009, 41 (10) :2051-2061
[100]   Role of murine cytomegalovirus US22 gene family members in replication in macrophages [J].
Ménard, C ;
Wagner, M ;
Ruzsics, Z ;
Holak, K ;
Brune, W ;
Campbell, AE ;
Koszinowski, UH .
JOURNAL OF VIROLOGY, 2003, 77 (10) :5557-5570