Reactive Oxygen Species (ROS) Regulates Different Types of Cell Death by Acting as a Rheostat

被引:287
作者
Villalpando-Rodriguez, Gloria E. [1 ,2 ]
Gibson, Spencer B. [1 ,2 ]
机构
[1] Univ Manitoba, Res Inst Oncol & Hematol, Canc Care Manitoba, Winnipeg, MB, Canada
[2] Univ Manitoba, Dept Biochem & Med Genet, Winnipeg, MB, Canada
关键词
NF-KAPPA-B; ACTIVATED PROTEIN-KINASE; ELECTRON-TRANSPORT-CHAIN; OXIDATIVE STRESS; INDUCED APOPTOSIS; SUPEROXIDE DISMUTASES; SIGNALING PLATFORM; HYDROGEN-PEROXIDE; DLG MOTIFS; VITAMIN-E;
D O I
10.1155/2021/9912436
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Reactive oxygen species (ROS) are essential for cellular signaling and response to stress. The level of ROS and the type of ROS determine the ability of cells to undergo cell death. Furthermore, dysregulation of the antioxidant pathways is associated with many diseases. It has become apparent that cell death can occur through different mechanisms leading to the classifications of different types of cell death such as apoptosis, ferroptosis, and necroptosis. ROS play essential roles in all forms of cell death, but it is only now coming into focus that ROS control and determine the type of cell death that occurs in any given cell. Indeed, ROS may act as a rheostat allowing different cell death mechanisms to be engaged and crosstalk with different cell death types. In this review, we will describe the ROS regulatory pathways and how they control different types of cell death under normal and disease states. We will also propose how ROS could provide a mechanism of crosstalk between cell death mechanisms and act as a rheostat determining the type of cell death.
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页数:17
相关论文
共 138 条
[1]   Mitochondria DNA deletions in atherosclerotic hypoperfused brain microvessels as a primary target for the development of Alzheimer's disease [J].
Aliyev, A ;
Chen, SG ;
Seyidova, D ;
Smith, MA ;
Perry, G ;
de la Torre, J ;
Aliev, G .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2005, 229 :285-292
[2]  
[Anonymous], 2007, ENCY STRESS
[3]  
[Anonymous], 1985, Oxidative Stress
[4]  
[Anonymous], 2008, PROGRAMMED CELL DEAT
[5]  
[Anonymous], 2019, Glutathione
[6]  
[Anonymous], 1997, OXYGEN RADICALS DIS
[7]   Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[8]   BIOLOGICAL DEFENSE MECHANISMS - PRODUCTION BY LEUKOCYTES OF SUPEROXIDE A POTENTIAL BACTERICIDAL AGENT [J].
BABIOR, BM ;
KIPNES, RS ;
CURNUTTE, JT .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (03) :741-744
[9]   Cysteine-mediated redox signalling in the mitochondria [J].
Bak, D. W. ;
Weerapana, E. .
MOLECULAR BIOSYSTEMS, 2015, 11 (03) :678-697
[10]   Mitochondrial complex I inhibition triggers a mitophagy-dependent ROS increase leading to necroptosis and ferroptosis in melanoma cells [J].
Basit, Farhan ;
van Oppen, Lisanne M. P. E. ;
Schoeckel, Laura ;
Bossenbroek, Hasse M. ;
van Emst-de Vries, Sjenet E. ;
Hermeling, Johannes C. W. ;
Grefte, Sander ;
Kopitz, Charlotte ;
Heroult, Melanie ;
Willems, Peter H. G. M. ;
Koopman, Werner J. H. .
CELL DEATH & DISEASE, 2017, 8 :e2716-e2716