Physiological consequences of programmed necrosis, an alternative form of cell demise

被引:24
作者
Cho, Young Sik [1 ]
Park, Seung Yeon [1 ]
Shin, Hee Suk [1 ]
Chan, Francis Ka-Ming [2 ]
机构
[1] Korea Res Inst Chem Technol, Bioorgan Sci Div, Pharmacol Res Ctr, Taejon 305600, South Korea
[2] Univ Massachusetts, Sch Med, Dept Pathol, Worcester, MA 01655 USA
关键词
apoptosis; inflammation; programmed necrosis; receptor interacting protein; TNF alpha; RECEPTOR-INTERACTING PROTEIN; APOPTOSIS-INDUCING FACTOR; POLY(ADP-RIBOSE) POLYMERASE-1; DEATH; INHIBITION; IDENTIFICATION; NECROPTOSIS; ACTIVATION; PATHWAYS; KINASE;
D O I
10.1007/s10059-010-0066-3
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
Cell death occurs spontaneously or in response to external stimuli, and can be largely subdivided into apoptosis and necrosis by the distinct morphological and biochemical features. Unlike apoptosis, necrosis was recognized as the passive and unwanted cell demise committed in a non-regulated and disorganized manner. However, under specific conditions such as caspase intervention, necrosis has been proposed to be regulated in a well-orchestrated way as a backup mechanism of apoptosis. The term programmed necrosis has been coined to describe such an alternative cell death. Recently, at least some regulators governing programmed necrosis have been identified and demonstrated to be interconnected via a wide network of signal pathways by further extensive studies. There is growing evidence that programmed necrosis is not only associated with pathophysiological diseases, but also provides innate immune response to viral infection. Here, we will introduce recent updates on the molecular mechanism and physiological significance of programmed necrosis.
引用
收藏
页码:327 / 332
页数:6
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