The cell on the edge of life and death: Crosstalk between autophagy and apoptosis

被引:67
作者
Kasprowska-Liskiewicz, Daniela [1 ]
机构
[1] Akad Wychowania Fizycznego Jerzego Kukuczki Katow, Lab Badan Mol, Katowice, Poland
来源
POSTEPY HIGIENY I MEDYCYNY DOSWIADCZALNEJ | 2017年 / 71卷
关键词
autophagy; apoptosis; BCL-2; family; p53; BCL-2; FAMILY-MEMBERS; ACTIVATED PROTEIN-KINASE; BECLIN; DAP-KINASE; MOLECULAR-MECHANISM; REGULATES AUTOPHAGY; MEDIATED CLEAVAGE; X-L; PHOSPHORYLATION; DEGRADATION;
D O I
10.5604/01.3001.0010.4672
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Recently, the crosstalk between autophagy and apoptosis has attracted broader attention. Basal autophagy serves to maintain cell homeostasis, while the upregulation of this process is an element of stress response that enables the cell to survive under adverse conditions. Autophagy may also determine the fate of the cell through its interactions with cell death pathways. The protein networks that control the initiation and the execution phase of these two processes are highly interconnected. Several scenarios for the crosstalk between autophagy and apoptosis exist. In most cases, the activation of autophagy represents an attempt of the cell to cope with stress, and protects the cell from apoptosis or delays its initiation. Generally, the simultaneous activation of pro-survival and pro-death pathways is prevented by the mutual inhibitory crosstalk between autophagy and apoptosis. But in some circumstances, autophagy or the proteins of the core autophagic machinery may promote cellular demise through excessive self-digestion (so-called "autophagic cell death") or by stimulating the activation of other cell death pathways. It is controversial whether cells actually die via autophagy, which is why the term "autophagic cell death" has been under intense debate lately. This review summarizes the recent findings on the multilevel crosstalk between autophagy and apoptosis in aspects of common regulators, mutual inhibition of these processes, the stimulation of apoptosis by autophagy or autophagic proteins and finally the role of autophagy as a death-execution mechanism.
引用
收藏
页码:825 / 841
页数:17
相关论文
共 103 条
[1]   Diversifying microRNA sequence and function [J].
Ameres, Stefan L. ;
Zamore, Phillip D. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2013, 14 (08) :475-488
[2]   Inhibition of hepatocyte autophagy increases tumor necrosis factor-dependent liver injury by promoting caspase-8 activation [J].
Amir, M. ;
Zhao, E. ;
Fontana, L. ;
Rosenberg, H. ;
Tanaka, K. ;
Gao, G. ;
Czaja, M. J. .
CELL DEATH AND DIFFERENTIATION, 2013, 20 (07) :878-887
[3]   Atg4D at the interface between autophagy and apoptosis [J].
Betin, Virginie M. S. ;
Lane, Jon D. .
AUTOPHAGY, 2009, 5 (07) :1057-1059
[4]   The role of cell signalling in the crosstalk between autophagy and apoptosis [J].
Booth, Laurence A. ;
Tavallai, Seyedmehrad ;
Hamed, Hossein A. ;
Cruickshanks, Nichola ;
Dent, Paul .
CELLULAR SIGNALLING, 2014, 26 (03) :549-555
[5]   Death-associated protein kinase (DAPK) and signal transduction: blebbing in programmed cell death [J].
Bovellan, Miia ;
Fritzsche, Marco ;
Stevens, Craig ;
Charras, Guillaume .
FEBS JOURNAL, 2010, 277 (01) :58-65
[6]   Beclin 1: a BH3-only protein that fails to induce apoptosis [J].
Boya, P. ;
Kroemer, G. .
ONCOGENE, 2009, 28 (21) :2125-2127
[7]   BAX and BAK1 are dispensable for ABT-737-induced dissociation of the BCL2-BECN1 complex and autophagy [J].
Bravo-San Pedro, Jose Manuel ;
Wei, Yongjie ;
Sica, Valentina ;
Maiuri, Maria Chiara ;
Zou, Zhongju ;
Kroemer, Guido ;
Levine, Beth .
AUTOPHAGY, 2015, 11 (03) :452-459
[8]   Global genomic profiling reveals an extensive p53-regulated autophagy program contributing to key p53 responses [J].
Broz, Daniela Kenzelmann ;
Mello, Stephano Spano ;
Bieging, Kathryn T. ;
Jiang, Dadi ;
Dusek, Rachel L. ;
Brady, Colleen A. ;
Sidow, Arend ;
Attardi, Laura D. .
GENES & DEVELOPMENT, 2013, 27 (09) :1016-1031
[9]   The regulation of autophagy - unanswered questions [J].
Chen, Yongqiang ;
Klionsky, Daniel J. .
JOURNAL OF CELL SCIENCE, 2011, 124 (02) :161-170
[10]   Bcl-2 complexed with Beclin-1 maintains full anti-apoptotic function [J].
Ciechomska, I. A. ;
Goemans, G. C. ;
Skepper, J. N. ;
Tolkovsky, A. M. .
ONCOGENE, 2009, 28 (21) :2128-2141