Oxidative Stress-Induced Cellular Senescence: Is Labile Iron the Connecting Link?

被引:42
作者
Nousis, Lambros [1 ]
Kanavaros, Panagiotis [2 ]
Barbouti, Alexandra [2 ]
机构
[1] Univ Ioannina, Fac Med, Sch Hlth Sci, Dept Hyg & Epidemiol, Ioannina 45110, Greece
[2] Univ Ioannina, Fac Med, Sch Hlth Sci, Dept Anat Histol Embryol, Ioannina 45110, Greece
关键词
oxidative stress; reactive oxygen species; labile iron; cellular senescence; telomeres; DNA-damage; lipofuscin; mitochondria; lysosomes; H2O2-INDUCED DNA-DAMAGE; LYSOSOMAL AXIS THEORY; HYDROGEN-PEROXIDE; MITOCHONDRIAL DYSFUNCTION; LIPOFUSCIN ACCUMULATION; TELOMERIC DNA; PREMATURE SENESCENCE; INTRACELLULAR IRON; CHELATABLE IRON; PROTECT CELLS;
D O I
10.3390/antiox12061250
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
Cellular senescence, a cell state characterized by a generally irreversible cell cycle arrest, is implicated in various physiological processes and a wide range of age-related pathologies. Oxidative stress, a condition caused by an imbalance between the production and the elimination of reactive oxygen species (ROS) in cells and tissues, is a common driver of cellular senescence. ROS encompass free radicals and other molecules formed as byproducts of oxygen metabolism, which exhibit varying chemical reactivity. A prerequisite for the generation of strong oxidizing ROS that can damage macromolecules and impair cellular function is the availability of labile (redox-active) iron, which catalyzes the formation of highly reactive free radicals. Targeting labile iron has been proven an effective strategy to counteract the adverse effects of ROS, but evidence concerning cellular senescence is sparse. In the present review article, we discuss aspects of oxidative stress-induced cellular senescence, with special attention to the potential implication of labile iron.
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页数:21
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共 159 条
[21]   Nox family NADPH oxidases: Molecular mechanisms of activation [J].
Brandes, Ralf P. ;
Weissmann, Norbert ;
Schroeder, Katrin .
FREE RADICAL BIOLOGY AND MEDICINE, 2014, 76 :208-226
[22]   Lipofuscin: Mechanisms of age-related accumulation and influence on cell function [J].
Brunk, UT ;
Terman, A .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (05) :611-619
[23]   The mitochondrial-lysosomal axis theory of aging - Accumulation of damaged mitochondria as a result of imperfect autophagocytosis [J].
Brunk, UT ;
Terman, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2002, 269 (08) :1996-2002
[24]   Labile iron in cells and body fluids: physiology, pathology, and pharmacology [J].
Cabantchik, Zvi Ioav .
FRONTIERS IN PHARMACOLOGY, 2014, 5
[25]   Oxidative DNA damage & repair: An introduction [J].
Cadet, Jean ;
Davies, Kelvin J. A. .
FREE RADICAL BIOLOGY AND MEDICINE, 2017, 107 :2-12
[26]   The biology of replicative senescence [J].
Campisi, J .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (05) :703-709
[27]   Aging, Cellular Senescence, and Cancer [J].
Campisi, Judith .
ANNUAL REVIEW OF PHYSIOLOGY, VOL 75, 2013, 75 :685-705
[28]   4-Hydroxynonenal (HNE) modified proteins in metabolic diseases [J].
Castro, Jose Pedro ;
Jung, Tobias ;
Grune, Tilman ;
Siems, Werner .
FREE RADICAL BIOLOGY AND MEDICINE, 2017, 111 :309-315
[29]   Targeting cellular senescence based on interorganelle communication, multilevel proteostasis, and metabolic control [J].
Cavinato, Maria ;
Madreiter-Sokolowski, Corina T. ;
Buettner, Sabrina ;
Schosserer, Markus ;
Zwerschke, Werner ;
Wedel, Sophia ;
Grillari, Johannes ;
Graier, Wolfgang F. ;
Jansen-Duerr, Pidder .
FEBS JOURNAL, 2021, 288 (12) :3834-3854
[30]   Reduction in mitochondrial iron alleviates cardiac damage during injury [J].
Chang, Hsiang-Chun ;
Wu, Rongxue ;
Shang, Meng ;
Sato, Tatsuya ;
Chen, Chunlei ;
Shapiro, Jason S. ;
Liu, Ting ;
Thakur, Anita ;
Sawicki, Konrad T. ;
Prasad, Sathyamangla V. N. ;
Ardehali, Hossein .
EMBO MOLECULAR MEDICINE, 2016, 8 (03) :247-267