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

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.

[1]  A. Goussia,et al.  Combined administration of membrane-permeable and impermeable iron-chelating drugs attenuates ischemia/reperfusion-induced hepatic injury. , 2022, Free radical biology & medicine.

[2]  K. Vávrová,et al.  Examination of diverse iron-chelating agents for the protection of differentiated PC12 cells against oxidative injury induced by 6-hydroxydopamine and dopamine , 2022, Scientific Reports.

[3]  K. Engeland Cell cycle regulation: p53-p21-RB signaling , 2022, Cell Death & Differentiation.

[4]  Aditi U. Gurkar,et al.  Lipids as Regulators of Cellular Senescence , 2022, Frontiers in Physiology.

[5]  F. d’Adda di Fagagna,et al.  Telomere dysfunction in ageing and age-related diseases , 2022, Nature Cell Biology.

[6]  J. Passos,et al.  Cellular senescence: all roads lead to mitochondria , 2022, The FEBS journal.

[7]  J. Campisi,et al.  The metabolic roots of senescence: mechanisms and opportunities for intervention , 2021, Nature Metabolism.

[8]  M. Kharchenko,et al.  Outcomes of Deferoxamine Action on H2O2-Induced Growth Inhibition and Senescence Progression of Human Endometrial Stem Cells , 2021, International journal of molecular sciences.

[9]  M. Bruchez,et al.  Telomeric 8-oxo-guanine drives rapid premature senescence in the absence of telomere shortening , 2021, Nature Structural & Molecular Biology.

[10]  E. Gilson,et al.  Neutrophils: mediating TelOxidation and senescence , 2021, The EMBO journal.

[11]  P. Jat,et al.  Mechanisms of Cellular Senescence: Cell Cycle Arrest and Senescence Associated Secretory Phenotype , 2021, Frontiers in Cell and Developmental Biology.

[12]  Shane A. Evans,et al.  Neutrophils induce paracrine telomere dysfunction and senescence in ROS‐dependent manner , 2021, The EMBO journal.

[13]  V. Gorgoulis,et al.  Implication of Dietary Iron-Chelating Bioactive Compounds in Molecular Mechanisms of Oxidative Stress-Induced Cell Ageing , 2021, Antioxidants.

[14]  Tim Baldensperger,et al.  Protein oxidation - Formation mechanisms, detection and relevance as biomarkers in human diseases , 2021, Redox biology.

[15]  M. Cavinato,et al.  Targeting cellular senescence based on interorganelle communication, multilevel proteostasis, and metabolic control , 2020, The FEBS journal.

[16]  K. Pantopoulos,et al.  Basics and principles of cellular and systemic iron homeostasis. , 2020, Molecular aspects of medicine.

[17]  Dean P. Jones,et al.  Reactive oxygen species (ROS) as pleiotropic physiological signalling agents , 2020, Nature Reviews Molecular Cell Biology.

[18]  B. Friguet,et al.  Proteome Oxidative Modifications and Impairment of Specific Metabolic Pathways During Cellular Senescence and Aging , 2020, Proteomics.

[19]  T. Grune Oxidized protein aggregates: Formation and biological effects. , 2020, Free radical biology & medicine.

[20]  N. Mizushima,et al.  Lysosome biology in autophagy , 2020, Cell Discovery.

[21]  V. Gorgoulis,et al.  Implications of Oxidative Stress and Cellular Senescence in Age-Related Thymus Involution , 2020, Oxidative medicine and cellular longevity.

[22]  M. Beekman,et al.  Senescent human melanocytes drive skin ageing via paracrine telomere dysfunction , 2019, The EMBO journal.

[23]  C. Schmitt,et al.  Cellular Senescence: Defining a Path Forward , 2019, Cell.

[24]  H. Ichijo,et al.  Iron homeostasis and iron-regulated ROS in cell death, senescence and human diseases. , 2019, Biochimica et biophysica acta. General subjects.

[25]  K. Pantopoulos,et al.  Iron homeostasis and oxidative stress: An intimate relationship. , 2019, Biochimica et biophysica acta. Molecular cell research.

[26]  E. Fielder,et al.  Mitochondrial dysfunction and cell senescence: deciphering a complex relationship , 2019, FEBS letters.

[27]  Simon C Watkins,et al.  Targeted and Persistent 8-Oxoguanine Base Damage at Telomeres Promotes Telomere Loss and Crisis. , 2019, Molecular cell.

[28]  J. Shay,et al.  Telomeres and telomerase: three decades of progress , 2019, Nature Reviews Genetics.

[29]  S. Cloonan,et al.  Mitochondrial Iron in Human Health and Disease. , 2019, Annual review of physiology.

[30]  Dean P. Jones,et al.  The Exposome: Molecules to Populations. , 2019, Annual review of pharmacology and toxicology.

[31]  V. Gorgoulis,et al.  In situ evidence of cellular senescence in Thymic Epithelial Cells (TECs) during human thymic involution , 2019, Mechanisms of Ageing and Development.

[32]  G. Gestri,et al.  Neuropilin-1 Controls Endothelial Homeostasis by Regulating Mitochondrial Function and Iron-Dependent Oxidative Stress , 2018, iScience.

[33]  V. Gladyshev,et al.  Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells , 2018, Aging cell.

[34]  S. Park,et al.  Adjustment of the lysosomal-mitochondrial axis for control of cellular senescence , 2018, Ageing Research Reviews.

[35]  M. Calero,et al.  An Overview of the Role of Lipofuscin in Age-Related Neurodegeneration , 2018, Front. Neurosci..

[36]  M. Demaria,et al.  Hallmarks of Cellular Senescence. , 2018, Trends in cell biology.

[37]  Susan Smith Telomerase can't handle the stress , 2018, Genes & development.

[38]  G. Marverti,et al.  Targeting Oxidatively Induced DNA Damage Response in Cancer: Opportunities for Novel Cancer Therapies , 2018, Oxidative medicine and cellular longevity.

[39]  Y. Suh,et al.  Age- and Tissue-Specific Expression of Senescence Biomarkers in Mice , 2018, Front. Genet..

[40]  A. Tzakos,et al.  Lipophilic ester and amide derivatives of rosmarinic acid protect cells against H2O2-induced DNA damage and apoptosis: The potential role of intracellular accumulation and labile iron chelation , 2018, Redox biology.

[41]  Gopal Jayaraj,et al.  Pathways of cellular proteostasis in aging and disease , 2018, The Journal of cell biology.

[42]  A. Stier,et al.  Does oxidative stress shorten telomeres in vivo? A review , 2017, Biology Letters.

[43]  A. Sfera,et al.  Ferrosenescence: The iron age of neurodegeneration? , 2017, Mechanisms of Ageing and Development.

[44]  B. Stockwell,et al.  Ferroptosis: A Regulated Cell Death Nexus Linking Metabolism, Redox Biology, and Disease , 2017, Cell.

[45]  Tobias Jung,et al.  4‐Hydroxynonenal (HNE) modified proteins in metabolic diseases , 2017, Free radical biology & medicine.

[46]  A. Bush,et al.  Iron accumulation in senescent cells is coupled with impaired ferritinophagy and inhibition of ferroptosis , 2017, Redox biology.

[47]  Caroline L. Wilson,et al.  Cellular senescence drives age-dependent hepatic steatosis , 2017, Nature Communications.

[48]  K. Davies,et al.  Oxidative DNA damage & repair: An introduction. , 2017, Free radical biology & medicine.

[49]  H. Griffiths,et al.  Lipid (per) oxidation in mitochondria: an emerging target in the ageing process? , 2017, Biogerontology.

[50]  V. Korolchuk,et al.  Mitochondria in Cell Senescence: Is Mitophagy the Weakest Link? , 2017, EBioMedicine.

[51]  Hanna Salmonowicz,et al.  Detecting senescence: a new method for an old pigment , 2017, Aging cell.

[52]  S. Rivella,et al.  A Red Carpet for Iron Metabolism , 2017, Cell.

[53]  Tobias Jung,et al.  Mitochondrial contribution to lipofuscin formation , 2017, Redox biology.

[54]  Zhe Wang,et al.  Autophagy impairment with lysosomal and mitochondrial dysfunction is an important characteristic of oxidative stress-induced senescence , 2017, Autophagy.

[55]  J. Lingner,et al.  Peroxiredoxin 1 Protects Telomeres from Oxidative Damage and Preserves Telomeric DNA for Extension by Telomerase. , 2016, Cell reports.

[56]  Tobias Jung,et al.  Happily (n)ever after: Aging in the context of oxidative stress, proteostasis loss and cellular senescence , 2016, Redox biology.

[57]  Dimitris Kletsas,et al.  Robust, universal biomarker assay to detect senescent cells in biological specimens , 2016, Aging cell.

[58]  Michalis D. Mantzaris,et al.  Hydroxytyrosol inhibits hydrogen peroxide-induced apoptotic signaling via labile iron chelation , 2016, Redox biology.

[59]  S. Myong,et al.  Oxidative guanine base damage regulates human telomerase activity , 2016, Nature Structural &Molecular Biology.

[60]  A. Thakur,et al.  Reduction in mitochondrial iron alleviates cardiac damage during injury , 2016, EMBO molecular medicine.

[61]  Ashley I Bush,et al.  Iron neurochemistry in Alzheimer's disease and Parkinson's disease: targets for therapeutics , 2016, Journal of neurochemistry.

[62]  Laura C. Greaves,et al.  Mitochondria are required for pro‐ageing features of the senescent phenotype , 2016, The EMBO journal.

[63]  A. Cuervo,et al.  Proteostasis and aging , 2015, Nature Network Boston.

[64]  D. Baker,et al.  Cellular senescence in aging and age-related disease: from mechanisms to therapy , 2015, Nature Medicine.

[65]  P. Townsend,et al.  The DNA damage response and immune signaling alliance: Is it good or bad? Nature decides when and where. , 2015, Pharmacology & therapeutics.

[66]  R. Morimoto,et al.  The biology of proteostasis in aging and disease. , 2015, Annual review of biochemistry.

[67]  V. Abbate,et al.  Iron-sensitive fluorescent probes: monitoring intracellular iron pools. , 2015, Metallomics : integrated biometal science.

[68]  M. Conrad,et al.  Glutathione peroxidase 4 (Gpx4) and ferroptosis: what's so special about it? , 2015, Molecular & cellular oncology.

[69]  H. Sies,et al.  Oxidative stress: a concept in redox biology and medicine , 2015, Redox biology.

[70]  A. Walch,et al.  Inactivation of the ferroptosis regulator Gpx4 triggers acute renal failure in mice , 2014, Nature Cell Biology.

[71]  R. Brandes,et al.  Nox family NADPH oxidases: Molecular mechanisms of activation. , 2014, Free radical biology & medicine.

[72]  F. d’Adda di Fagagna,et al.  Stable Cellular Senescence Is Associated with Persistent DDR Activation , 2014, PloS one.

[73]  Manuel Serrano,et al.  Cellular senescence: from physiology to pathology , 2014, Nature Reviews Molecular Cell Biology.

[74]  N. Chandel,et al.  ROS Function in Redox Signaling and Oxidative Stress , 2014, Current Biology.

[75]  P. Gonzalez-Cabo,et al.  Mitochondrial dysfunction induced by frataxin deficiency is associated with cellular senescence and abnormal calcium metabolism , 2014, Front. Cell. Neurosci..

[76]  Antonio Ayala,et al.  Lipid Peroxidation: Production, Metabolism, and Signaling Mechanisms of Malondialdehyde and 4-Hydroxy-2-Nonenal , 2014, Oxidative medicine and cellular longevity.

[77]  Z. Cabantchik Labile iron in cells and body fluids: physiology, pathology, and pharmacology , 2014, Front. Pharmacol..

[78]  M. Narita,et al.  Cellular senescence and its effector programs , 2014, Genes & development.

[79]  W. Koppenol,et al.  The complex interplay of iron metabolism, reactive oxygen species, and reactive nitrogen species: insights into the potential of various iron therapies to induce oxidative and nitrosative stress. , 2013, Free radical biology & medicine.

[80]  J. Sharpe,et al.  Senescence Is a Developmental Mechanism that Contributes to Embryonic Growth and Patterning , 2013, Cell.

[81]  Manuel Serrano,et al.  The Hallmarks of Aging , 2013, Cell.

[82]  S. Verhulst,et al.  Telomere length behaves as biomarker of somatic redundancy rather than biological age , 2013, Aging cell.

[83]  J. Campisi Aging, cellular senescence, and cancer. , 2013, Annual review of physiology.

[84]  T. Grune,et al.  Lipofuscin: formation, effects and role of macroautophagy☆ , 2013, Redox biology.

[85]  Michalis D. Mantzaris,et al.  Lipophilic caffeic acid derivatives protect cells against H2O2-Induced DNA damage by chelating intracellular labile iron. , 2012, Journal of agricultural and food chemistry.

[86]  Kerstin Schneeberger,et al.  Telomerase gene therapy in adult and old mice delays aging and increases longevity without increasing cancer , 2012, EMBO molecular medicine.

[87]  C. Lawless,et al.  A senescent cell bystander effect: senescence-induced senescence , 2012, Aging cell.

[88]  F. D. D. Fagagna,et al.  Telomeric DNA damage is irreparable and causes persistent DNA-damage-response activation , 2012, Nature Cell Biology.

[89]  Clara Correia-Melo,et al.  Telomeres are favoured targets of a persistent DNA damage response in ageing and stress-induced senescence , 2012, Nature Communications.

[90]  J. Campisi,et al.  Four faces of cellular senescence , 2011, The Journal of cell biology.

[91]  V. Lobo,et al.  Free radicals, antioxidants and functional foods: Impact on human health , 2010, Pharmacognosy reviews.

[92]  O. Soehnlein,et al.  Phagocyte partnership during the onset and resolution of inflammation , 2010, Nature Reviews Immunology.

[93]  E. Gilson,et al.  TRF2/RAP1 and DNA–PK mediate a double protection against joining at telomeric ends , 2010, The EMBO journal.

[94]  Tobias Jung,et al.  Lipofuscin-bound iron is a major intracellular source of oxidants: role in senescent cells. , 2010, Free radical biology & medicine.

[95]  Anil Wipat,et al.  Feedback between p21 and reactive oxygen production is necessary for cell senescence , 2010, Molecular systems biology.

[96]  E. Arriaga,et al.  Mitochondrial turnover and aging of long-lived postmitotic cells: the mitochondrial-lysosomal axis theory of aging. , 2010, Antioxidants & redox signaling.

[97]  L. Valenti,et al.  Tumorigenesis and Neoplastic Progression Iron-Dependent Regulation of MDM2 Influences p53 Activity and Hepatic Carcinogenesis , 2010 .

[98]  Margaret A. Strong,et al.  Short telomeres are sufficient to cause the degenerative defects associated with aging. , 2009, American journal of human genetics.

[99]  T. de Lange How Telomeres Solve the End-Protection Problem , 2009, Science.

[100]  G. Ferbeyre,et al.  Mitochondrial Dysfunction Contributes to Oncogene-Induced Senescence , 2009, Molecular and Cellular Biology.

[101]  Michael P. Murphy,et al.  How mitochondria produce reactive oxygen species , 2008, The Biochemical journal.

[102]  H. Chung,et al.  Mitochondrial iron accumulation with age and functional consequences , 2008, Aging cell.

[103]  U. Brunk,et al.  Lysosomes in iron metabolism, ageing and apoptosis , 2008, Histochemistry and Cell Biology.

[104]  K. Pantopoulos,et al.  Oxidative Stress and Iron Homeostasis: Mechanistic and Health Aspects , 2008 .

[105]  E. Kolettas,et al.  Hydrogen peroxide inhibits caspase-dependent apoptosis by inactivating procaspase-9 in an iron-dependent manner. , 2007, Free radical biology & medicine.

[106]  Tilman Grune,et al.  Lipofuscin: formation, distribution, and metabolic consequences. , 2007, Annals of the New York Academy of Sciences.

[107]  M. Blasco,et al.  Telomere length, stem cells and aging. , 2007, Nature chemical biology.

[108]  U. Brunk,et al.  Autophagy, ageing and apoptosis: the role of oxidative stress and lysosomal iron. , 2007, Archives of biochemistry and biophysics.

[109]  T. Kirkwood,et al.  Mitochondrial Dysfunction Accounts for the Stochastic Heterogeneity in Telomere-Dependent Senescence , 2007, PLoS biology.

[110]  W. Zwerschke,et al.  Sustained inhibition of oxidative phosphorylation impairs cell proliferation and induces premature senescence in human fibroblasts , 2006, Experimental Gerontology.

[111]  F. Petrat,et al.  Chelation and determination of labile iron in primary hepatocytes by pyridinone fluorescent probes. , 2006, The Biochemical journal.

[112]  U. Brunk,et al.  Oxidative stress, accumulation of biological 'garbage', and aging. , 2006, Antioxidants & redox signaling.

[113]  K. Riganakos,et al.  Protection against nuclear DNA damage offered by flavonoids in cells exposed to hydrogen peroxide: the role of iron chelation. , 2005, Free radical biology & medicine.

[114]  T. Lange,et al.  Shelterin: the protein complex that shapes and safeguards human telomeres , 2005 .

[115]  D. Galaris,et al.  DNA protecting and genotoxic effects of olive oil related components in cells exposed to hydrogen peroxide , 2005, Free radical research.

[116]  U. Brunk,et al.  Role of compartmentalized redox-active iron in hydrogen peroxide-induced DNA damage and apoptosis. , 2005, The Biochemical journal.

[117]  Jinshui Fan,et al.  Oxidative damage in telomeric DNA disrupts recognition by TRF1 and TRF2 , 2005, Nucleic acids research.

[118]  S. Jackson,et al.  Functional links between telomeres and proteins of the DNA-damage response. , 2004, Genes & development.

[119]  P. Jansen-Dürr,et al.  Senescence-associated changes in respiration and oxidative phosphorylation in primary human fibroblasts. , 2004, The Biochemical journal.

[120]  B. Ames,et al.  Iron Accumulation during Cellular Senescence , 2004, Annals of the New York Academy of Sciences.

[121]  S. Oikawa,et al.  Mechanism of Telomere Shortening by Oxidative Stress , 2004, Annals of the New York Academy of Sciences.

[122]  John M Sedivy,et al.  Telomere shortening triggers senescence of human cells through a pathway involving ATM, p53, and p21(CIP1), but not p16(INK4a). , 2004, Molecular cell.

[123]  N. Carter,et al.  A DNA damage checkpoint response in telomere-initiated senescence , 2003, Nature.

[124]  J. Turrens,et al.  Mitochondrial formation of reactive oxygen species , 2003, The Journal of physiology.

[125]  S. Christoforidis,et al.  Endosomal and lysosomal effects of desferrioxamine: protection of HeLa cells from hydrogen peroxide-induced DNA damage and induction of cell-cycle arrest. , 2003, Free radical biology & medicine.

[126]  G. Saretzki,et al.  MitoQ counteracts telomere shortening and elongates lifespan of fibroblasts under mild oxidative stress , 2003, Aging cell.

[127]  T. Tsuzuki,et al.  Oxidative nucleotide damage: consequences and prevention , 2002, Oncogene.

[128]  Or Kakhlon,et al.  The labile iron pool: characterization, measurement, and participation in cellular processes(1). , 2002, Free radical biology & medicine.

[129]  C. Chi,et al.  Increase in mitochondrial mass in human fibroblasts under oxidative stress and during replicative cell senescence. , 2002, Journal of biomedical science.

[130]  U. Brunk,et al.  Lipofuscin: mechanisms of age-related accumulation and influence on cell function. , 2002, Free radical biology & medicine.

[131]  U. Brunk,et al.  The mitochondrial-lysosomal axis theory of aging: accumulation of damaged mitochondria as a result of imperfect autophagocytosis. , 2002, European journal of biochemistry.

[132]  B. Frei,et al.  Intracellular iron, but not copper, plays a critical role in hydrogen peroxide-induced DNA damage. , 2001, Free radical biology & medicine.

[133]  T. Zglinicki,et al.  Lipofuscin accumulation in proliferating fibroblasts in vitro: an indicator of oxidative stress , 2001, Experimental Gerontology.

[134]  K. Davies Oxidative Stress, Antioxidant Defenses, and Damage Removal, Repair, and Replacement Systems , 2000, IUBMB life.

[135]  S. Oikawa,et al.  Site‐specific DNA damage at GGG sequence by oxidative stress may accelerate telomere shortening , 1999, FEBS letters.

[136]  M. Blasco,et al.  Disease states associated with telomerase deficiency appear earlier in mice with short telomeres , 1999, The EMBO journal.

[137]  J. Griffith,et al.  Mammalian Telomeres End in a Large Duplex Loop , 1999, Cell.

[138]  F. Petrat,et al.  Determination of the chelatable iron pool of isolated rat hepatocytes by digital fluorescence microscopy using the fluorescent probe, phen green SK , 1999, Hepatology.

[139]  Sandy Chang,et al.  Longevity, Stress Response, and Cancer in Aging Telomerase-Deficient Mice , 1999, Cell.

[140]  J. Campisi The biology of replicative senescence. , 1997, European journal of cancer.

[141]  G. Saretzki,et al.  Mild hyperoxia shortens telomeres and inhibits proliferation of fibroblasts: a model for senescence? , 1995, Experimental cell research.

[142]  P. Kruk,et al.  DNA damage and repair in telomeres: relation to aging. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[143]  D. McLachlan,et al.  Intramuscular desferrioxamine in patients with Alzheimer's disease , 1991, The Lancet.

[144]  C. Harley,et al.  Telomeres shorten during ageing of human fibroblasts , 1990, Nature.

[145]  R. S. Sohal,et al.  Effect of ferric iron and desferrioxamine on lipofuscin accumulation in cultured rat heart myocytes , 1988, Mechanisms of Ageing and Development.

[146]  S. Linn,et al.  Toxic DNA damage by hydrogen peroxide through the Fenton reaction in vivo and in vitro. , 1988, Science.

[147]  A M Olovnikov,et al.  A theory of marginotomy. The incomplete copying of template margin in enzymic synthesis of polynucleotides and biological significance of the phenomenon. , 1973, Journal of theoretical biology.

[148]  J. D. Watson Origin of Concatemeric T7DNA , 1972 .

[149]  L. Hayflick,et al.  The serial cultivation of human diploid cell strains. , 1961, Experimental cell research.

[150]  J. Lingner,et al.  Impact of oxidative stress on telomere biology. , 2018, Differentiation; research in biological diversity.

[151]  I. Wittig,et al.  Generator-specific targets of mitochondrial reactive oxygen species. , 2015, Free radical biology & medicine.

[152]  L. Defebvre,et al.  Targeting Chelatable Iron as a Therapeutic Modality in Parkinson ’ s Disease , 2016 .

[153]  D. Galaris,et al.  Protective Effects of Olive Oil Components Against Hydrogen Peroxide-Induced DNA Damage: The Potential Role of Iron Chelation , 2010 .

[154]  T. de Lange,et al.  Shelterin: the protein complex that shapes and safeguards human telomeres. , 2005, Genes & development.

[155]  T. von Zglinicki Oxidative stress shortens telomeres. , 2002, Trends in biochemical sciences.

[156]  T. Zglinicki,et al.  Accumulation of single-strand breaks is the major cause of telomere shortening in human fibroblasts. , 2000, Free radical biology & medicine.

[157]  T. Zglinicki,et al.  Lipofuscin accumulation and ageing of fibroblasts. , 1995, Gerontology.

[158]  M Chevion,et al.  A site-specific mechanism for free radical induced biological damage: the essential role of redox-active transition metals. , 1988, Free radical biology & medicine.