Iron homeostasis and oxidative stress: An intimate relationship

被引:658
作者
Galaris, Dimitrios [1 ]
Barbouti, Alexandra [2 ]
Pantopoulos, Kostas [3 ,4 ]
机构
[1] Univ Ioannina, Sch Med, Biol Chem Lab, Ioannina, Greece
[2] Univ Ioannina, Sch Med, Dept Anat Histol Embryol, Ioannina, Greece
[3] McGill Univ, Lady Davis Inst Med Res, Montreal, PQ, Canada
[4] McGill Univ, Dept Med, Montreal, PQ, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2019年 / 1866卷 / 12期
基金
加拿大健康研究院;
关键词
Iron metabolism; Oxygen; Oxidative stress; Redox signaling; Ferroptosis; Lipid peroxidation; NF-KAPPA-B; ADHESION MOLECULE EXPRESSION; HYPOXIA-INDUCIBLE FACTORS; H2O2-INDUCED DNA-DAMAGE; TRANSFERRIN RECEPTOR 1; HYDROGEN-PEROXIDE; REGULATORY PROTEIN-1; CELL-DEATH; INTRACELLULAR IRON; LIPID-PEROXIDATION;
D O I
10.1016/j.bbamcr.2019.118535
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
Iron is a transition metal and essential constituent of almost all living cells and organisms. As component of various metalloproteins it is involved in critical biochemical processes such as transport of oxygen in tissues, electron transfer reactions during respiration in mitochondria, synthesis and repair of DNA, metabolism of xenobiotics, etc. However, when present in excess within cells and tissues, iron disrupts redox homeostasis and catalyzes the propagation of reactive oxygen species (ROS), leading to oxidative stress. ROS are critical for physiological signaling pathways, but oxidative stress is associated with tissue injury and disease. At the cellular level, oxidative stress may lead to ferroptosis, an iron-dependent form of cell death. In this review, we focus on the intimate relationship between iron metabolism and oxidative stress in health and disease. We discuss aspects of redox- and iron-mediated signaling, toxicity, ferroptotic cell death, homeostatic pathways and pathophysiological implications.
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页数:15
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共 193 条
[21]   Free radical biology - terminology and critical thinking [J].
Azzi, A ;
Davies, KJA ;
Kelly, F .
FEBS LETTERS, 2004, 558 (1-3) :3-6
[22]   Intracellular iron, but not copper, plays a critical role in hydrogen peroxide-induced DNA damage [J].
Barbouti, A ;
Doulias, PT ;
Zhu, BZ ;
Frei, B ;
Galaris, D .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 31 (04) :490-498
[23]   Hydrogen peroxide inhibits caspase-dependent apoptosis by inactivating procaspase-9 in an iron-dependent manner [J].
Barbouti, Alexandra ;
Amorgianiotis, Christos ;
Kolettas, Evangelos ;
Kanavaros, Panagiotis ;
Galaris, Dimitrios .
FREE RADICAL BIOLOGY AND MEDICINE, 2007, 43 (10) :1377-1387
[24]   Regulation of PTP1B via glutathionylation of the active site cysteine 215 [J].
Barrett, WC ;
DeGnore, JP ;
König, S ;
Fales, HM ;
Keng, YF ;
Zhang, ZY ;
Yim, MB ;
Chock, PB .
BIOCHEMISTRY, 1999, 38 (20) :6699-6705
[25]   Iron neurochemistry in Alzheimer's disease and Parkinson's disease: targets for therapeutics [J].
Belaidi, Abdel A. ;
Bush, Ashley I. .
JOURNAL OF NEUROCHEMISTRY, 2016, 139 :179-197
[26]   Glutathione peroxidases [J].
Brigelius-Flohe, Regina ;
Maiorino, Matilde .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2013, 1830 (05) :3289-3303
[27]   Haemochromatosis [J].
Brissot, Pierre ;
Pietrangelo, Antonello ;
Adams, Paul C. ;
de Graaff, Barbara ;
McLaren, Christine E. ;
Loreal, Olivier .
NATURE REVIEWS DISEASE PRIMERS, 2018, 4
[28]   Non-transferrin bound iron: A key role in iron overload and iron toxicity [J].
Brissot, Pierre ;
Ropert, Martine ;
Le Lan, Caroline ;
Loreal, Olivier .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2012, 1820 (03) :403-410
[29]   Iron-Chelating Therapy for Transfusional Iron Overload [J].
Brittenham, Gary M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (02) :146-156
[30]   THE PECKING ORDER OF FREE-RADICALS AND ANTIOXIDANTS - LIPID-PEROXIDATION, ALPHA-TOCOPHEROL, AND ASCORBATE [J].
BUETTNER, GR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 300 (02) :535-543