Blue Light Induces Mitochondrial DNA Damage and Free Radical Production in Epithelial Cells*

Exposure of biological chromophores to ultraviolet radiation can lead to photochemical damage. However, the role of visible light, particularly in the blue region of the spectrum, has been largely ignored. To test the hypothesis that blue light is toxic to non-pigmented epithelial cells, confluent cultures of human primary retinal epithelial cells were exposed to visible light (390–550 nm at 2.8 milliwatts/cm2) for up to 6 h. A small loss of mitochondrial respiratory activity was observed at 6 h compared with dark-maintained cells, and this loss became greater with increasing time. To investigate the mechanism of cell loss, the damage to mitochondrial and nuclear genes was assessed using the quantitative PCR. Light exposure significantly damaged mitochondrial DNA at 3 h (0.7 lesion/10 kb DNA) compared with dark-maintained controls. However, by 6 h of light exposure, the number of lesions was decreased in the surviving cells, indicating DNA repair. Isolated mitochondria exposed to light generated singlet oxygen, superoxide anion, and the hydroxyl radical. Antioxidants confirmed the superoxide anion to be the primary species responsible for the mitochondrial DNA lesions. The effect of lipofuscin, a photoinducible intracellular generator of reactive oxygen intermediates, was investigated for comparison. Exposure of lipofuscin-containing cells to visible light caused an increase in both mitochondrial and nuclear DNA lesions compared with non-pigmented cells. We conclude that visible light can cause cell dysfunction through the action of reactive oxygen species on DNA and that this may contribute to cellular aging, age-related pathologies, and tumorigenesis.

[1]  I. Kraljić,et al.  A NEW METHOD FOR THE DETECTION OF SINGLET OXYGEN IN AQUEOUS SOLUTIONS , 1978 .

[2]  B. Halliwell,et al.  Superoxide-dependent formation of hydroxyl radicals: detection of hydroxyl radicals by the hydroxylation of aromatic compounds. , 1981, Analytical biochemistry.

[3]  R. Tyrrell,et al.  LETHAL ACTION OF ULTRAVIOLET AND VISIBLE (BLUE‐VIOLET) RADIATIONS AT DEFINED WAVELENGTHS ON HUMAN LYMPHOBLASTOID CELLS: ACTION SPECTRA AND INTERACTION SITES , 1984, Photochemistry and photobiology.

[4]  N. Krinsky,et al.  Superoxide anion is generated from cellular metabolites by solar radiation and its components. , 1985, Journal of free radicals in biology & medicine.

[5]  M. Peak,et al.  INDUCTION OF DNA‐PROTEIN CROSSLINKS IN HUMAN CELLS BY ULTRAVIOLET and VISIBLE RADIATIONS: ACTION SPECTRUM , 1985, Photochemistry and photobiology.

[6]  E. Huberman,et al.  Mutagenesis and cytotoxicity in human epithelial cells by far- and near-ultraviolet radiations: action spectra. , 1987, Radiation research.

[7]  J. Vamecq,et al.  Pathophysiology of peroxisomal beta-oxidation. , 1989, Essays in biochemistry.

[8]  P. Newburger,et al.  Measurement of superoxide release in the phagovacuoles of immune complex-stimulated human neutrophils. , 1990, Journal of immunological methods.

[9]  M. Peak,et al.  HYDROXYL RADICAL QUENCHING AGENTS PROTECT AGAINST DNA BREAKAGE CAUSED BY BOTH 365‐nm UVA AND BY GAMMA RADIATION , 1990, Photochemistry and photobiology.

[10]  J. L. Emmerson,et al.  Genotoxicity studies on the preemergence herbicide trifluralin. , 1991, Mutation research.

[11]  R Lubart,et al.  Effects of visible and near-infrared lasers on cell cultures. , 1992, Journal of photochemistry and photobiology. B, Biology.

[12]  P. Söderberg,et al.  Cytochrome oxidase activity in rat retina after exposure to 404 nm blue light. , 1992, Current eye research.

[13]  M. Boulton,et al.  Lipofuscin is a photoinducible free radical generator. , 1993, Journal of photochemistry and photobiology. B, Biology.

[14]  J. Chappell,et al.  Dihydrorhodamine 123: a fluorescent probe for superoxide generation? , 1993, European journal of biochemistry.

[15]  R. Setlow,et al.  Wavelengths effective in induction of malignant melanoma. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[16]  G F Vrensen,et al.  Blue-light-induced dysfunction of the blood-retinal barrier at the pigment epithelium in albino versus pigmented rabbits. , 1994, Experimental eye research.

[17]  K. Davies,et al.  Adaptive response and oxidative stress. , 1994, Environmental health perspectives.

[18]  R. Setlow,et al.  Temporal changes in the incidence of malignant melanoma: explanation from action spectra. , 1994, Mutation research.

[19]  V. Massey Activation of molecular oxygen by flavins and flavoproteins. , 1994, The Journal of biological chemistry.

[20]  M. Boulton,et al.  Blue Light-induced Reactivity of Retinal Age Pigment , 1995, The Journal of Biological Chemistry.

[21]  M. Peak,et al.  INDUCTION OF SLOWLY DEVELOPING ALKALI‐LABILE SITES IN HUMAN P3 CELL DNA BY UVA AND BLUE‐ AND GREEN‐LIGHT PHOTONS: ACTION SPECTRUM , 1995, Photochemistry and photobiology.

[22]  B. Van Houten,et al.  Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[23]  U. Brunk,et al.  Lipofuscin accumulation in cultured retinal pigment epithelial cells causes enhanced sensitivity to blue light irradiation. , 1997, Free radical biology & medicine.

[24]  Chang-an Yu,et al.  Generation of Superoxide Anion by Succinate-Cytochromec Reductase from Bovine Heart Mitochondria* , 1998, The Journal of Biological Chemistry.

[25]  Takashi Tokoro,et al.  Observation of ultrastructural changes in cultured retinal pigment epithelium following exposure to blue light , 1998, Graefe's Archive for Clinical and Experimental Ophthalmology.

[26]  B. Epe,et al.  Oxidative DNA damage induced by visible light in mammalian cells: extent, inhibition by antioxidants and genotoxic effects. , 1998, Mutation research.

[27]  B. Godley,et al.  Hydrogen peroxide causes significant mitochondrial DNA damage in human RPE cells. , 1999, Experimental eye research.

[28]  R. Stierum,et al.  Mitochondrial DNA repair pathways. , 1999, Journal of bioenergetics and biomembranes.

[29]  Timothy A. Skimina,et al.  Activation of flavin-containing oxidases underlies light-induced production of H2O2 in mammalian cells. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[30]  T. Tokoro,et al.  Processes of blue light-induced damage to retinal pigment epithelial cells lacking phagosomes. , 1999, Japanese journal of ophthalmology.

[31]  S. Davies,et al.  Photodamage to human RPE cells by A2-E, a retinoid component of lipofuscin. , 2000, Investigative ophthalmology & visual science.

[32]  B. Godley,et al.  Hydrogen peroxide stimulates apoptosis in cultured human retinal pigment epithelial cells , 2001, Current eye research.

[33]  R. Aebersold,et al.  The mitochondrial antioxidant defence system and its response to oxidative stress , 2001, Proteomics.

[34]  G. Dianov,et al.  Base excision repair in nuclear and mitochondrial DNA. , 2001, Progress in nucleic acid research and molecular biology.

[35]  F. A. Shamsi,et al.  Photocytotoxicity of lipofuscin in human retinal pigment epithelial cells. , 2001, Free radical biology & medicine.

[36]  F. A. Shamsi,et al.  Inhibition of RPE lysosomal and antioxidant activity by the age pigment lipofuscin. , 2001, Investigative ophthalmology & visual science.

[37]  H. Remmen,et al.  Oxidative damage to mitochondria and aging , 2001, Experimental Gerontology.

[38]  S. Ledoux,et al.  Base excision repair of mitochondrial DNA damage in mammalian cells. , 2001, Progress in nucleic acid research and molecular biology.

[39]  V. Bunik,et al.  Inactivation of the 2-oxo acid dehydrogenase complexes upon generation of intrinsic radical species. , 2002, European journal of biochemistry.

[40]  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.

[41]  Yau-Huei Wei,et al.  Oxidative Stress, Mitochondrial DNA Mutation, and Impairment of Antioxidant Enzymes in Aging 1 , 2002, Experimental biology and medicine.

[42]  V. Kagan,et al.  Toward Mechanism‐based Antioxidant Interventions , 2002, Annals of the New York Academy of Sciences.

[43]  B. Van Houten,et al.  Mitochondrial DNA repair and aging. , 2002, Mutation research.

[44]  Chi-Hung Lin,et al.  Critical role of mitochondrial reactive oxygen species formation in visible laser irradiation-induced apoptosis in rat brain astrocytes (RBA-1). , 2002, Journal of Biomedical Sciences.

[45]  M. Goyns Genes, telomeres and mammalian ageing , 2002, Mechanisms of Ageing and Development.

[46]  E. R. Taylor,et al.  Superoxide Activates Uncoupling Proteins by Generating Carbon-centered Radicals and Initiating Lipid Peroxidation , 2003, Journal of Biological Chemistry.

[47]  N. Hamasaki,et al.  Mitochondrial Oxidative Stress and Mitochondrial DNA , 2003, Clinical chemistry and laboratory medicine.

[48]  A. Takeshita,et al.  Oxidative Stress Mediates Tumor Necrosis Factor-&agr;–Induced Mitochondrial DNA Damage and Dysfunction in Cardiac Myocytes , 2003, Circulation.

[49]  T. Kaneko,et al.  Protective effects of flavonoids on the cytotoxicity of linoleic acid hydroperoxide toward rat pheochromocytoma PC12 cells. , 2003, Chemico-biological interactions.

[50]  G. Cecchini,et al.  Function and structure of complex II of the respiratory chain. , 2003, Annual review of biochemistry.

[51]  G. Vrensen,et al.  Spectral sensitivity of the blood-retinal barrier at the pigment epithelium for blue light in the 400–500 nm range , 1993, Graefe's Archive for Clinical and Experimental Ophthalmology.

[52]  B. Epe,et al.  Reactive oxygen species derived from the mitochondrial respiratory chain are not responsible for the basal levels of oxidative base modifications observed in nuclear DNA of Mammalian cells. , 2004, Free radical biology & medicine.

[53]  Cristina Bianchi,et al.  The Mitochondrial Production of Reactive Oxygen Species in Relation to Aging and Pathology , 2004, Annals of the New York Academy of Sciences.

[54]  Effects of Flavonoids on the Resistance of Microsomes to Lipid Peroxidation In Vitro and Ex Vivo , 2003, Bulletin of Experimental Biology and Medicine.

[55]  T. Peng,et al.  Mitochondrial Swelling and Generation of Reactive Oxygen Species Induced by Photoirradiation Are Heterogeneously Distributed , 2004, Annals of the New York Academy of Sciences.

[56]  E. Gottlieb,et al.  Mitochondria-derived Reactive Oxygen Species Mediate Blue Light–induced Death of Retinal Pigment Epithelial Cells¶ , 2004, Photochemistry and photobiology.

[57]  Yau-Huei Wei,et al.  Mitochondrial alterations, cellular response to oxidative stress and defective degradation of proteins in aging , 2004, Biogerontology.

[58]  Brian Herman,et al.  Oxidative stress-induced apoptosis is associated with alterations in mitochondrial caspase activity and Bcl-2-dependent alterations in mitochondrial pH (pHm) , 2004, Brain Research Bulletin.

[59]  T. Peng,et al.  Visualization of the antioxidative effects of melatonin at the mitochondrial level during oxidative stress‐induced apoptosis of rat brain astrocytes , 2004, Journal of pineal research.