Necroptosis: An emerging type of cell death in liver diseases

被引:55
作者
Saeed, Waqar Khalid [1 ]
Jun, Dae Won [1 ]
机构
[1] Hanyang Univ, Sch Med, Dept Gastroenterol, Seoul 133070, South Korea
关键词
Necroptosis; Programmed necrosis; Apoptosis; Cell death; Liver disease; RECEPTOR-INTERACTING PROTEIN; MIXED-LINEAGE KINASE; ISCHEMIA-REPERFUSION INJURY; PROGRAMMED NECROSIS; MOLECULAR SWITCH; DOMAIN-LIKE; TNF-ALPHA; APOPTOSIS; RIP1; MICE;
D O I
10.3748/wjg.v20.i35.12526
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Cell death has been extensively evaluated for decades and it is well recognized that pharmacological interventions directed to inhibit cell death can prevent significant cell loss and can thus improve an organ' s physiological function. For long, only apoptosis was considered as a sole form of programmed cell death. Recently necroptosis, a RIP1/RIP3-dependent programmed cell death, has been identified as an apoptotic backup cell death mechanism with necrotic morphology. The evidences of necroptosis and protective effects achieved by blocking necroptosis have been extensively reported in recent past. However, only a few studies reported the evidence of necroptosis and protective effects achieved by inhibiting necroptosis in liver related disease conditions. Although the number of necroptosis initiators is increasing; however, interestingly, it is still unclear that what actually triggers necroptosis in different liver diseases or if there is always a different necroptosis initiator in each specific disease condition followed by specific downstream signaling molecules. Understanding the precise mechanism of necroptosis as well as counteracting other cell death pathways in liver diseases could provide a useful insight towards achieving extensive therapeutic significance. By targeting necroptosis and/or other parallel death pathways, a significant cell loss and thus a decrement in an organ's physiological function can be prevented. (C) 2014 Baishideng Publishing Group Inc. All rights reserved.
引用
收藏
页码:12526 / 12532
页数:7
相关论文
共 51 条
[1]
ARC is a novel therapeutic approach against acetaminophen-induced hepatocellular necrosis [J].
An, Junfeng ;
Mehrhof, Felix ;
Harms, Christoph ;
Laettig-Tuennemann, Gisela ;
Lee, Sabrina L. L. ;
Endres, Matthias ;
Li, Mingyi ;
Sellge, Gernot ;
Mandic, Ana D. ;
Trautwein, Christian ;
Donath, Stefan .
JOURNAL OF HEPATOLOGY, 2013, 58 (02) :297-305
[2]
NEMO and RIP1 Control Cell Fate in Response to Extensive DNA Damage via TNF-α Feedforward Signaling [J].
Biton, Sharon ;
Ashkenazi, Avi .
CELL, 2011, 145 (01) :92-103
[3]
A role for tumor necrosis factor receptor-2 and receptor-interacting protein in programmed necrosis and antiviral responses [J].
Chan, FKM ;
Shisler, J ;
Bixby, JG ;
Felices, M ;
Zheng, LX ;
Appel, M ;
Orenstein, J ;
Moss, B ;
Lenardo, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (51) :51613-51621
[4]
Anti-Necroptosis Chemical Necrostatin-1 Can Also Suppress Apoptotic and Autophagic Pathway to Exert Neuroprotective Effect in Mice Intracerebral Hemorrhage Model [J].
Chang, Pan ;
Dong, Wenwen ;
Zhang, Mingyang ;
Wang, Zufeng ;
Wang, Yaoqi ;
Wang, Tao ;
Gao, Yuan ;
Meng, Huanhuan ;
Luo, Bin ;
Luo, Chengliang ;
Chen, Xiping ;
Tao, Luyang .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2014, 52 (02) :242-249
[5]
RIP1-Dependent and Independent Effects of Necrostatin-1 in Necrosis and T Cell Activation [J].
Cho, YoungSik ;
McQuade, Thomas ;
Zhang, Haibing ;
Zhang, Jianke ;
Chan, Francis Ka-Ming .
PLOS ONE, 2011, 6 (08)
[6]
Phosphorylation-Driven Assembly of the RIP1-RIP3 Complex Regulates Programmed Necrosis and Virus-Induced Inflammation [J].
Cho, YoungSik ;
Challa, Sreerupa ;
Moquin, David ;
Genga, Ryan ;
Ray, Tathagat Dutta ;
Guildford, Melissa ;
Chan, Francis Ka-Ming .
CELL, 2009, 137 (06) :1112-1123
[7]
Chemical inhibitor of nonapoptotic cell death with therapeutic potential for ischemic brain injury [J].
Degterev A. ;
Huang Z. ;
Boyce M. ;
Li Y. ;
Jagtap P. ;
Mizushima N. ;
Cuny G.D. ;
Mitchison T.J. ;
Moskowitz M.A. ;
Yuan J. .
Nature Chemical Biology, 2005, 1 (2) :112-119
[8]
Expansion and evolution of cell death programmes [J].
Degterev, Alexei ;
Yuan, Junying .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2008, 9 (05) :378-390
[9]
Identification of RIP1 kinase as a specific cellular target of necrostatins [J].
Degterev, Alexei ;
Hitomi, Junichi ;
Germscheid, Megan ;
Ch'en, Irene L. ;
Korkina, Olga ;
Teng, Xin ;
Abbott, Derek ;
Cuny, Gregory D. ;
Yuan, Chengye ;
Wagner, Gerhard ;
Hedrick, Stephen M. ;
Gerber, Scott A. ;
Lugovskoy, Alexey ;
Yuan, Junying .
NATURE CHEMICAL BIOLOGY, 2008, 4 (05) :313-321
[10]
Ferroptosis: An Iron-Dependent Form of Nonapoptotic Cell Death [J].
Dixon, Scott J. ;
Lemberg, Kathryn M. ;
Lamprecht, Michael R. ;
Skouta, Rachid ;
Zaitsev, Eleina M. ;
Gleason, Caroline E. ;
Patel, Darpan N. ;
Bauer, Andras J. ;
Cantley, Alexandra M. ;
Yang, Wan Seok ;
Morrison, Barclay, III ;
Stockwell, Brent R. .
CELL, 2012, 149 (05) :1060-1072