Programmed Necrosis, Not Apoptosis, in the Heart

被引:228
作者
Kung, Gloria
Konstantinidis, Klitos
Kitsis, Richard N. [1 ]
机构
[1] Albert Einstein Coll Med, Wilf Family Cardiovasc Res Inst, Bronx, NY 10461 USA
关键词
cell death; necrosis; apoptosis; myocardial infarction; heart failure; MITOCHONDRIAL PERMEABILITY TRANSITION; NECROTIC CELL-DEATH; ADENINE-NUCLEOTIDE TRANSLOCASE; LYSOSOMAL MEMBRANE PERMEABILIZATION; ISCHEMIA-REPERFUSION INJURY; ACUTE MYOCARDIAL-INFARCTION; ENDOPLASMIC-RETICULUM CA2+; ELECTRON-TRANSPORT CHAIN; C-EPSILON INTERACTS; FAILING HUMAN HEART;
D O I
10.1161/CIRCRESAHA.110.225730
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is well known that apoptosis is an actively mediated cell suicide process. In contrast, necrosis, a morphologically distinct form of cell death, has traditionally been regarded as passive and unregulated. Over the past decade, however, experiments in Caenorhabditis elegans and mammalian cells have revealed that a significant proportion of necrotic death is, in fact, actively mediated by the doomed cell. Although a comprehensive understanding of necrosis is still lacking, some key molecular events have come into focus. Cardiac myocyte apoptosis and necrosis are prominent features of the major cardiac syndromes. Accordingly, the recognition of necrosis as a regulated process mandates a reexamination of cell death in the heart. This review discusses pathways that mediate programmed necrosis, how they intersect with apoptotic pathways, roles of necrosis in heart disease, and new therapeutic opportunities that the regulated nature of necrosis presents. (Circ Res. 2011;108:1017-1036.)
引用
收藏
页码:1017 / 1036
页数:20
相关论文
共 180 条
  • [71] Fas triggers an alternative, caspase-8-independent cell death pathway using the kinase RIP as effector molecule
    Holler, N
    Zaru, R
    Micheau, O
    Thome, M
    Attinger, A
    Valitutti, S
    Bodmer, JL
    Schneider, P
    Seed, B
    Tschopp, J
    [J]. NATURE IMMUNOLOGY, 2000, 1 (06) : 489 - 495
  • [72] HUNTER FE, 1955, J BIOL CHEM, V216, P357
  • [73] Phospholipase A(2) is necessary for tumor necrosis factor alpha-induced ceramide generation in L929 cells
    Jayadev, S
    Hayter, HL
    Andrieu, N
    Gamard, CJ
    Liu, B
    Balu, R
    Hayakawa, M
    Ito, F
    Hannun, YA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (27) : 17196 - 17203
  • [74] Jeremias I, 2000, CIRCULATION, V102, P915
  • [75] Glycogen synthase kinase-3β mediates convergence of protection signaling to inhibit the mitochondrial permeability transition pore
    Juhaszova, M
    Zorov, DB
    Kim, SH
    Pepe, S
    Fu, Q
    Fishbein, KW
    Ziman, BD
    Wang, S
    Ytrehus, K
    Antos, CL
    Olson, EN
    Sollott, SJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (11) : 1535 - 1549
  • [76] Kajstura J, 1996, LAB INVEST, V74, P86
  • [77] μ-Calpain mediated cleavage of the Na+/Ca2+ exchanger in isolated mitochondria under A23187 induced Ca2+ stimulation
    Kar, Pulak
    Chakraborti, Tapati
    Samanta, Krishna
    Chakraborti, Sajal
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2009, 482 (1-2) : 66 - 76
  • [78] Calpain inhibition reduces infarct size and improves global hemodynamics and left ventricular contractility in a porcine myocardial ischemia/reperfusion model
    Khalil, PN
    Neuhof, C
    Huss, R
    Pollhammer, M
    Khalil, MN
    Neuhof, H
    Fritz, H
    Siebeck, M
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2005, 528 (1-3) : 124 - 131
  • [79] Cytosolic phospholipase A2, lipoxygenase metabolites, and reactive oxygen species
    Kim, Cheolmin
    Kim, Joo-Young
    Kim, Jae-Hong
    [J]. BMB REPORTS, 2008, 41 (08) : 555 - 559
  • [80] TNF-induced activation of the Nox1 NADPH oxidase and its role in the induction of necrotic cell death
    Kim, You-Sun
    Morgan, Michael J.
    Choksi, Swati
    Liu, Zheng-Gang
    [J]. MOLECULAR CELL, 2007, 26 (05) : 675 - 687