Dynamics of H2O2 availability to ARPE-19 cultures in models of oxidative stress

Free Radical Biology and Medicine

Volumn 48, Issue 8, 2010, Pages 1064-1070

  Kaczara, Patrycja ^a   Sarna, Tadeusz ^a   Burke, Janice M ^b  

^a JAGIELLONIAN UNIVERSITY   (Poland)

^b MEDICAL COLLEGE OF WISCONSIN   (United States)

Author keywords

ARPE 19 cells; Free radicals; Glucose oxidase; Hydrogen peroxide; Oxidative stress

Indexed keywords

GLUCOSE OXIDASE; HYDROGEN PEROXIDE;

ARTICLE; CELL AGING; CELL CULTURE; CELL DAMAGE; CHRONIC STRESS; CONTROLLED STUDY; CYTOTOXICITY; HUMAN; HUMAN CELL; MEMBRANE DAMAGE; OXIDATIVE STRESS; PIGMENT EPITHELIUM; PRIORITY JOURNAL; CELL LINE; METABOLISM; PHYSIOLOGY;

CELL LINE; GLUCOSE OXIDASE; HUMANS; HYDROGEN PEROXIDE; OXIDATIVE STRESS; PIGMENT EPITHELIUM OF EYE; RETINAL PIGMENT EPITHELIUM;

EID: 77950520685     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2010.01.022     Document Type: Article

References (50)

1. Cai J., Nelson K.C., Wu M., Sternberg P., Jones D.P. Oxidative damage and protection of the RPE. Prog. Retinal Eye Res. 2000, 19:205-221.
2. Beatty S., Koh H.-H., Henson D., Boulton M. The role of oxidative stress in the pathogenesis of age-related macular degeneration. Surv. Ophthalmol. 2000, 45:115-134.
3. Zarbin M.A. Current concepts in the pathogenesis of age-related macular degeneration. Arch. Ophthalmol. 2004, 122:598-614.
4. Algvere P.V., Marshall J., Seregard S. Age-related maculopathy and the impact of blue light hazard. Acta Ophthalmol. Scand. 2006, 84:4-15.
5. Wu J., Seregard S., Algvere P.V. Photochemical damage of the retina. Surv. Ophthalmol. 2006, 51:461-481.
6. Miceli M.V., Liles M.R., Newsome D.A. Evaluation of oxidative processes in human pigment epithelial cells associated with retinal outer segment phagocytosis. Exp. Cell Res. 1994, 214:242-249.
7. Sarna T., Burke J.M., Korytowski W., ŔZanowska M., Skumatz C.M.B, Zareba A., Zareba M. Loss of melanin from human RPE with aging: possible role of melanin photooxidation. Exp. Eye Res. 2003, 76:89-98.
8. Korytowski W., Pilas B., Sarna T., Kalyanaraman B. Photoinduced generation of hydrogen peroxide and hydroxyl radicals in melanins. Photochem. Photobiol. 1987, 45:185-190.
9. Zareba M., Raciti M.W., Henry M.M., Sarna T., Burke J.M. Oxidative stress in ARPE-19 cultures: do melanosomes confer cytoprotection?. Free Radic. Biol. Med. 2006, 40:87-100.
10. Ballinger S.W., Van Houten B., Jin G.-F., Conklin C.A., Godley B.F. Hydrogen peroxide causes significant mitochondrial DNA damage in human RPE cells. Exp. Eye Res. 1999, 68:765-772.
11. Geiger R.C., Waters C.M., Kamp D.W., Glucksberg M.R. KGF prevents oxygen-mediated damage in ARPE-19 cells. Invest. Ophthalmol. Visual Sci. 2005, 46:3435-3442.
12. Yang P., Peairs J.J., Tano R., Jaffe G.J. Oxidant-mediated Act activation in human RPE cells. Invest. Ophthalmol. Visual Sci. 2006, 47:4598-4606.
13. Kim M.-H., Chung J., Yang J., Chung S.-M., Kwag N.-H., Yoo J.-S. Hydrogen peroxide-induced cell death in a human retinal pigment epithelial cell line, ARPE-19. Korean J. Ophthalmol. 2003, 17:19-28.
14. 2-, HNE-, or tBH-treated ARPE-19 cells. Free Radic. Biol. Med. 2002, 33:1419-1432.
15. Alizadeh M., Wada M., Gelfman C.M., Handa J.T., Hjelmeland L.M. Downregulation of differentiation specific gene expression by oxidative stress in ARPE-19 cells. Invest. Ophthalmol. Visual Sci. 2001, 42:2706-2713.
16. Tsao Y.-P., Ho T.-C., Chen S.-L., Cheng H.-C. Pigment epithelium-derived factor inhibits oxidative stress-induced cell death by activation of extracellular signal-regulated kinases in cultured retinal pigment epithelial cells. Life Sci. 2006, 79:545-550.
17. Bienert G.P., Schjoerring J.K., Jahn T.P. Membrane transport of hydrogen peroxide. Biochim. Biophys. Acta 2006, 1758:994-1003.
18. Halliwell B., Clement M.V., Long L.H. Hydrogen peroxide in the human body. FEBS Lett. 2000, 486:10-13.
19. Winterbourn C.C. Hydroxyl radical production in body fluids: roles of metal ions, ascorbate and superoxide. Biochem. J. 1981, 198:125-131.
20. Wang X., Martindale J.L., Liu Y., Holbrook N.J. The cellular response to oxidative stress: influences of mitogen-activated protein kinase signaling pathways on cell survival. Biochem. J. 1998, 333:291-300.
21. Arnold R.S., Shi J., Murad E., Whalen A.M., Sun C.Q., Polavarapu R., Parthasarathy S., Petros J.A., Lambeth J.D. Hydrogen peroxide mediates the cell growth and transformation caused by the mitogenic oxidase Nox1. Proc. Natl. Acad. Sci. USA 2001, 98:5550-5555.
22. Rhee S.G., Bae Y.S., Lee S.-R., Kwon J. Hydrogen peroxide: a key messenger that modulates protein phosphorylation through cysteine oxidation. Sci. STKE 2000, 2000:1-6.
23. Hensley K., Robinson K.A., Gabbita S.P., Salsman S., Floyd R.A. Reactive oxygen species, cell signaling, and cell injury. Free Radic. Biol. Med. 2000, 28:1456-1462.
24. 2 permeation through cytoplasmic and peroxisomal membranes: comparison with experimental data. Biochim. Biophys. Acta 2004, 1673:149-159.
25. Makino N., Mise T., Sagara J.-i. Kinetics of hydrogen peroxide elimination by astrocytes and C6 glioma cells: analysis based on a mathematical model. Biochim. Biophys. Acta 2008, 1780:927-936.
26. Nowak D. Hydrogen peroxide release from human polymorphonuclear leukocytes measured with horseradish peroxidase and o-dianisidine: effect of various stimulators and cytochalasin B. Biomed. Biochim. Acta 1990, 49:353-362.
27. Nourooz-Zadeh J., Tajaddini-Sarmadi J., Wolff S.P. Measurement of plasma hydroperoxide concentrations by the ferrous oxidation-xylenol orange assay in conjunction with triphenylphosphine. Anal. Biochem. 1994, 220:403-409.
28. Banerjee D., Kumar P.A., Kumar B., Madhusoodanan U.K., Nayak S., Jacob J. Determination of absolute hydrogen peroxide concentration by spectrophotometric method. Curr. Sci. 2002, 83:1193-1194.
29. Verleur N., Wanders R.J.A. Permeability properties of peroxisomes in digitonin-permeabilized rat hepatocytes: evidence for free permeability towards a variety of substrates. Eur. J. Biochem. 1993, 218:75-82.
30. 2 gradients across biomembranes. FEBS Lett. 2000, 475:121-126.
31. Hamsley A., Pegg M., Crane D., Masters C. On the compartmentalization of catalase, fatty acyl-CoA oxidase and urate oxidase in mammalian livers, and the influence of clofibrate treatment on this microlocalization. Mol. Cell. Biochem. 1988, 83:187-194.
32. Long L.H., Evans P.J., Halliwell B. Hydrogen peroxide in human urine: implications for antioxidant defense and redox regulation. Biochem. Biophys. Res. Commun. 1999, 262:605-609.
33. Kim Y.H., Berry A.H., Spencer D.S., Stites W.E. Comparing the effect on protein stability of methionine oxidation versus mutagenesis: steps toward engineering oxidative resistance in proteins. Protein Eng. 2001, 14:343-347.
34. Shechter Y., Burstein Y., Patchornik A. Selective oxidation of methionine residues in proteins. Biochemistry 1975, 14:4497-4503.
35. Qin S., De Vries G.W. α2 but not α1 AMP-activated protein kinase mediates oxidative stress-induced inhibition of retinal pigment epithelium cell phagocytosis of photoreceptor outer segments. J. Biol. Chem. 2008, 283:6744-6751.
36. Meyskens F.L., Chau H.V., Tohidian N., Buckmeier J. Luminol-enhanced chemiluminescent response of human melanocytes and melanoma cells to hydrogen peroxide stress. Pigment Cell Res. 1997, 10:184-189.
37. 2 is a consequence of lysosomal rupture. Biochem. J. 2001, 356:549-555.
38. Zhang X., Zhou J., Fernandes A.F., Sparrow J.R., Pereira P., Taylor A., Shang F. The proteasome: a target of oxidative damage in cultured human retina pigment epithelial cells. Invest. Ophthalmol. Visual Sci. 2008, 49:3622-3630.
39. Kleppe K. The effect of hydrogen peroxide on glucose oxidase from Aspergillus niger. Biochemistry 1966, 5:139-143.
40. Bao J., Furumoto K., Yoshimoto M., Fukunaga K., Nakao K. Competitive inhibition by hydrogen peroxide produced in glucose oxidation catalyzed by glucose oxidase. Biochem. Eng. J. 2003, 13:69-72.
41. Zhu D., Tan K.S., Zhang X., Sun A.Y., Sun G.Y., Lee J.C.-M. Hydrogen peroxide alters membrane and cytoskeleton properties and increases intercellular connections in astrocytes. J. Cell Sci. 2005, 118:3695-3703.
42. Horowitz L.D., Wallner J.S., Decker D.E., Buxser S.E. Efficacy of lipid soluble, membrane-protective agents against hydrogen peroxide cytotoxicity in cardiac myocytes. Free Radic. Biol. Med. 1996, 21:743-753.
43. Block E.R. Hydrogen peroxide alters the physical state and function of the plasma membrane of pulmonary artery endothelial cells. J. Cell. Physiol. 1991, 146:362-369.
44. Jarret S.G., Boulton M.E. Antioxidant up-regulation and increased nuclear DNA protection play key roles in adaptation to oxidative stress in epithelial cells. Free Radic. Biol. Med. 2005, 38:1382-1391.
45. Treichel J.L., Henry M.M., Skumatz C.M.B., Eells J.T., Burke J.M. Antioxidants and ocular cell type differences in cytoprotection from formic acid toxicity in vitro. Toxicol. Sci. 2004, 82:183-192.
46. Bucolo C., Drago F., Lin L.-R., Reddy V.N. Neuroactive steroids protect retinal pigment epithelium against oxidative stress. Neuroreport 2005, 16:1203-1207.
47. Lukinova N., Iacovelli J., Dentchev T., Wolkow N., Hunter A., Amado D., Ying G.-S., Sparrow J.R., Dunaief J.L. Iron chelation protects the retinal pigment epithelial cell line ARPE-19 against cell death triggered by diverse stimuli. Invest. Ophthalmol. Visual Sci. 2009, 50:1440-1447.
48. Zhu D.-H., Wu J., Spee C., Ryan S.J., Hinton D.R. BMP4 mediates oxidative stress-induced retinal pigment epithelial cell senescence and is overexpressed in age-related macular degeneration. J. Biol. Chem 2009, 284:9529-9539.
49. Zareba M., Sarna T., Szewczyk G., Burke J.M. Photobleaching of melanosomes from retinal pigment epithelium. II. Effects on the response of living cells to photic stress. Photochem. Photobiol. 2007, 83:925-930.
50. Burke J.M., Zareba M. Sublethal photic stress and the motility of RPE phagosomes and melanosomes. Invest. Ophthalmol. Visual Sci. 2009, 50:1940-1947.