The interplay between nitric oxide and peroxiredoxins

Immunobiology

Volumn 213, Issue 9-10, 2008, Pages 815-822

  Abbas, Kahina ^a   Breton, Jacques ^a   Drapier, Jean Claude ^a  

^a CNRS   (France)

Author keywords

Immunostimulation; Macrophage; Nitric oxide; Peroxiredoxins; Redox signaling; Sulfiredoxin

Indexed keywords

CYSTEINE; HYDROGEN PEROXIDE; N METHYL DEXTRO ASPARTIC ACID; NITRIC OXIDE; PEROXIDE; PEROXIREDOXIN; PEROXYNITRITE; REACTIVE OXYGEN METABOLITE; SULFENIC ACID DERIVATIVE;

AMINO TERMINAL SEQUENCE; CATALYSIS; CYTOTOXICITY; DOPAMINERGIC NERVE CELL; ENZYME ACTIVITY; ENZYME INACTIVATION; EUKARYOTE; IMMUNOSTIMULATION; MACROPHAGE; MAMMAL; NONHUMAN; OXIDATION; OXIDATION REDUCTION STATE; OXIDATIVE STRESS; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROTEIN EXPRESSION; REDUCTION; REVIEW; SIGNAL TRANSDUCTION; YEAST;

ANIMALS; GENE EXPRESSION REGULATION; HUMANS; HYDROGEN PEROXIDE; MACROPHAGES; MICE; NITRIC OXIDE; OXIDATION-REDUCTION; OXIDATIVE STRESS; PEROXIREDOXINS; PROTEIN ISOFORMS; PROTEIN PROCESSING, POST-TRANSLATIONAL; SULFINIC ACIDS;

EID: 52749093875     PISSN: 01712985     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.imbio.2008.07.029     Document Type: Review

References (60)

1. Alamillo J.M., and Garcia-Olmedo F. Effects of urate, a natural inhibitor of peroxynitrite-mediated toxicity, in the response of Arabidopsis thaliana to the bacterial pathogen Pseudomonas syringae. Plant J. 25 (2001) 529-540
2. Bedard K., and Krause K.H. The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiol. Rev. 87 (2007) 245-313
3. Biteau B., Labarre J., and Toledano M.B. ATP-dependent reduction of cysteine-sulphinic acid by S. cerevisiae sulphiredoxin. Nature 425 (2003) 980-984
4. Bryk R., Griffin P., and Nathan C. Peroxynitrite reductase activity of bacterial peroxiredoxins. Nature 407 (2000) 211-215
5. Budanov A.V., Sablina A.A., Feinstein E., Koonin E.V., and Chumakov P.M. Regeneration of peroxiredoxins by p53-regulated sestrins, homologs of bacterial AhpD. Science 304 (2004) 596-600
6. Chang T.S., Jeong W., Choi S.Y., Yu S., Kang S.W., and Rhee S.G. Regulation of peroxiredoxin I activity by Cdc2-mediated phosphorylation. J. Biol. Chem. 277 (2002) 25370-25376
7. Chang T.S., Jeong W., Woo H.A., Lee S.M., Park S., and Rhee S.G. Characterization of mammalian sulfiredoxin and its reactivation of hyperoxidized peroxiredoxin through reduction of cysteine sulfinic acid in the active site to cysteine. J. Biol. Chem. 279 (2004) 50994-51001
8. Diet A., Abbas K., Bouton C., Guillon B., Tomasello F., Fourquet S., Toledano M.B., and Drapier J.C. Regulation of peroxiredoxins by nitric oxide in immunostimulated macrophages. J. Biol. Chem. 282 (2007) 36199-36205
9. Drapier J.C., and Bouton C. Modulation by nitric oxide of metalloprotein regulatory activities. Bioessays 18 (1996) 549-556
10. Dubuisson M., Vander Stricht D., Clippe A., Etienne F., Nauser T., Kissner R., Koppenol W.H., Rees J.F., and Knoops B. Human peroxiredoxin 5 is a peroxynitrite reductase. FEBS Lett. 571 (2004) 161-165
11. Ehrt S., Schnappinger D., Bekiranov S., Drenkow J., Shi S., Gingeras T.R., Gaasterland T., Schoolnik G., and Nathan C. Reprogramming of the macrophage transcriptome in response to interferon-gamma and Mycobacterium tuberculosis: signaling roles of nitric oxide synthase-2 and phagocyte oxidase. J. Exp. Med. 194 (2001) 1123-1140
12. Fang J., Nakamura T., Cho D.H., Gu Z., and Lipton S.A. S-nitrosylation of peroxiredoxin 2 promotes oxidative stress-induced neuronal cell death in Parkinson's disease. Proc. Natl. Acad. Sci. USA 104 (2007) 18742-18747
13. Fernandez-Tome P., Lizasoain I., Leza J.C., Lorenzo P., and Moro M.A. Neuroprotective effects of DETA-NONOate, a nitric oxide donor, on hydrogen peroxide-induced neurotoxicity in cortical neurones. Neuropharmacology 38 (1999) 1307-1315
14. Findlay V.J., Townsend D.M., Morris T.E., Fraser J.P., He L., and Tew K.D. A novel role for human sulfiredoxin in the reversal of glutathionylation. Cancer Res. 66 (2006) 6800-6806
15. Finkel T. Oxygen radicals and signaling. Curr. Opinion Cell Biol. 10 (1998) 248-253
16. Forman H.J., Torres M., and Fukuto J. Redox signaling. Mol. Cell. Biochem. 234-235 (2002) 49-62
17. Gallagher B.M., and Phelan S.A. Investigating transcriptional regulation of Prdx6 in mouse liver cells. Free Radical Biol. Med. 42 (2007) 1270-1277
18. Geremia E., Baratta D., Zafarana S., Giordano R., Pinizzotto M.R., La Rosa M.G., and Garozzo A. Antioxidant enzymatic systems in neuronal and glial cell-enriched fractions of rat brain during aging. Neurochem. Res. 15 (1990) 719-723
19. Gorbunov N.V., Yalowich J.C., Gaddam A., Thampatty P., Ritov V.B., Kisin E.R., Elsayed N.M., and Kagan V.E. Nitric oxide prevents oxidative damage produced by tert-butyl hydroperoxide in erythroleukemia cells via nitrosylation of heme and non-heme iron. Electron paramagnetic resonance evidence. J. Biol. Chem. 272 (1997) 12328-12341
20. Hirotsu S., Abe Y., Okada K., Nagahara N., Hori H., Nishino T., and Hakoshima T. Crystal structure of a multifunctional 2-Cys peroxiredoxin heme-binding protein 23 kDa/proliferation-associated gene product. Proc. Natl. Acad. Sci. USA 96 (1999) 12333-12338
21. Hofseth L.J., Robles A.I., Espey M.G., and Harris C.C. Nitric oxide is a signaling molecule that regulates gene expression. Methods Enzymol. 396 (2005) 326-340
22. Immenschuh S., and Baumgart-Vogt E. Peroxiredoxins, oxidative stress, and cell proliferation. Antioxid. Redox Signal 7 (2005) 768-777
23. Immenschuh S., Tan M., and Ramadori G. Nitric oxide mediates the lipopolysaccharide dependent upregulation of the heme oxygenase-1 gene expression in cultured rat Kupffer cells. J. Hepatol. 30 (1999) 61-69
24. Ishii T., Itoh K., Sato H., and Bannai S. Oxidative stress-inducible proteins in macrophages. Free Radical Res. 31 (1999) 351-355
25. Ishii T., Itoh K., Takahashi S., Sato H., Yanagawa T., Katoh Y., Bannai S., and Yamamoto M. Transcription factor Nrf2 coordinately regulates a group of oxidative stress-inducible genes in macrophages. J. Biol. Chem. 275 (2000) 16023-16029
26. Jaffrey, S.R., Snyder, S.H., 2001. The biotin switch method for the detection of S-nitrosylated proteins. Science STKE 2001, PL1.
27. Jang H.H., Lee K.O., Chi Y.H., Jung B.G., Park S.K., Park J.H., Lee J.R., Lee S.S., Moon J.C., Yun J.W., Choi Y.O., Kim W.Y., Kang J.S., Cheong G.W., Yun D.J., Rhee S.G., Cho M.J., and Lee S.Y. Two enzymes in one; two yeast peroxiredoxins display oxidative stress-dependent switching from a peroxidase to a molecular chaperone function. Cell 117 (2004) 625-635
28. Kamata H., Honda S., Maeda S., Chang L., Hirata H., and Karin M. Reactive oxygen species promote TNFalpha-induced death and sustained JNK activation by inhibiting MAP kinase phosphatases. Cell 20 (2005) 649-661
29. Kanner J., Harel S., and Granit R. Nitric oxide as an antioxidant. Arch. Biochem. Biophys. 289 (1991) 130-136
30. Komaki-Yasuda K., Kawazu S., and Kano S. Disruption of the Plasmodium falciparum 2-Cys peroxiredoxin gene renders parasites hypersensitive to reactive oxygen and nitrogen species. FEBS Lett. 547 (2003) 140-144
31. Kropotov A., Usmanova N., Serikov V., Zhivotovsky B., and Tomilin N. Mitochondrial targeting of human peroxiredoxin V protein and regulation of PRDX5 gene expression by nuclear transcription factors controlling biogenesis of mitochondria. FEBS J. 274 (2007) 5804-5814
32. Leslie N.R., Bennett D., Lindsay Y.E., Stewart H., Gray A., and Downes C.P. Redox regulation of PI 3-kinase signalling via inactivation of PTEN. EMBO J. 22 (2003) 5501-5510
33. Mitsumoto A., Takanezawa Y., Okawa K., Iwamatsu A., and Nakagawa Y. Variants of peroxiredoxins expression in response to hydroperoxide stress. Free Radical Biol. Med. 30 (2001) 625-635
34. 2-induced cell death. J. Biol. Chem. 280 (2005) 28775-28784
35. Mowbray A.L., Kang D.H., Rhee S.G., Kang S.W., and Jo H. Laminar shear stress up-regulates peroxiredoxins (PRX) in endothelial cells: PRX 1 as a mechanosensitive antioxidant. J. Biol. Chem. 283 (2008) 1622-1627
36. Nathan C., and Shiloh M.U. Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens. Proc. Natl. Acad. Sci. USA 97 (2000) 8841-8848
37. Neumann C.A., Krause D.S., Carman C.V., Das S., Dubey D.P., Abraham J.L., Bronson R.T., Fujiwara Y., Orkin S.H., and Van Etten R.A. Essential role for the peroxiredoxin Prdx1 in erythrocyte antioxidant defence and tumour suppression. Nature 424 (2003) 561-565
38. Perry T.L., Godin D.V., and Hansen S. Parkinson's disease: a disorder due to nigral glutathione deficiency?. Neurosci. Lett. 33 (1982) 305-310
39. 2 is not reflected in its reaction with other oxidants and thiol reagents. J. Biol. Chem. 282 (2007) 11885-11892
40. Peterson T.M., and Luckhart S. A mosquito 2-Cys peroxiredoxin protects against nitrosative and oxidative stresses associated with malaria parasite infection. Free Radical Biol. Med. 40 (2006) 1067-1082
41. Phalen T.J., Weirather K., Deming P.B., Anathy V., Howe A.K., van der Vliet A., Jonsson T.J., Poole L.B., and Heintz N.H. Oxidation state governs structural transitions in peroxiredoxin II that correlate with cell cycle arrest and recovery. J. Cell Biol. 175 (2006) 779-789
42. Philbert M.A., Beiswanger C.M., Waters D.K., Reuhl K.R., and Lowndes H.E. Cellular and regional distribution of reduced glutathione in the nervous system of the rat: histochemical localization by mercury orange and o-phthaldialdehyde-induced histofluorescence. Toxicol. Appl. Pharmacol. 107 (1991) 215-227
43. Poole L.B., and Nelson K.J. Discovering mechanisms of signaling-mediated cysteine oxidation. Curr. Opinion Chem. Biol. 12 (2008) 18-24
44. 2, a necessary evil for cell signaling. Science 312 (2006) 1882-1883
45. Rhee S.G., Chae H.Z., and Kim K. Peroxiredoxins: a historical overview and speculative preview of novel mechanisms and emerging concepts in cell signaling. Free Radical Biol. Med. 38 (2005) 1543-1552
46. Rhee S.G., Kang S.W., Jeong W., Chang T.S., Yang K.S., and Woo H.A. Intracellular messenger function of hydrogen peroxide and its regulation by peroxiredoxins. Curr. Opinion Cell Biol. 17 (2005) 183-189
47. Romero-Puertas M.C., Laxa M., Matte A., Zaninotto F., Finkemeier I., Jones A.M., Perazzolli M., Vandelle E., Dietz K.J., and Delledonne M. S-nitrosylation of peroxiredoxin II E promotes peroxynitrite-mediated tyrosine nitration. Plant Cell 19 (2007) 4120-4130
48. Sato D., Yanaka A., Shibahara T., Matsui H., Nakahara A., Yanagawa T., Warabi E., Ishii T., and Hyodo I. Peroxiredoxin I protects gastric mucosa from oxidative injury induced by H. pylori infection. J. Gastroenterol. Hepatol. (2007)
49. Shiloh M.U., and Nathan C.F. Reactive nitrogen intermediates and the pathogenesis of Salmonella and mycobacteria. Curr. Opinion Microbiol. 3 (2000) 35-42
50. Sian J., Dexter D.T., Lees A.J., Daniel S., Agid Y., Javoy-Agid F., Jenner P., and Marsden C.D. Alterations in glutathione levels in Parkinson's disease and other neurodegenerative disorders affecting basal ganglia. Ann. Neurol. 36 (1994) 348-355
51. Stamler J.S., Lamas S., and Fang F.C. Nitrosylation. The prototypic redox-based signaling mechanism. Cell 106 (2001) 675-683
52. Sun J., Steenbergen C., and Murphy E. S-nitrosylation: NO-related redox signaling to protect against oxidative stress. Antioxid. Redox Signal 8 (2006) 1693-1705
53. Thomas D.D., Ridnour L.A., Espey M.G., Donzelli S., Ambs S., Hussain S.P., Harris C.C., DeGraff W., Roberts D.D., Mitchell J.B., and Wink D.A. Superoxide fluxes limit nitric oxide-induced signaling. J. Biol. Chem. 281 (2006) 25984-25993
54. Trujillo M., Clippe A., Manta B., Ferrer-Sueta G., Smeets A., Declercq J.P., Knoops B., and Radi R. Pre-steady state kinetic characterization of human peroxiredoxin 5: taking advantage of Trp84 fluorescence increase upon oxidation. Arch. Biochem. Biophys. 467 (2007) 95-106
55. Wang X., Phelan S.A., Forsman-Semb K., Taylor E.F., Petros C., Brown A., Lerner C.P., and Paigen B. Mice with targeted mutation of peroxiredoxin 6 develop normally but are susceptible to oxidative stress. J. Biol. Chem. 278 (2003) 25179-25190
56. Wink D.A., Hanbauer I., Krishna M.C., DeGraff W., Gamson J., and Mitchell J.B. Nitric oxide protects against cellular damage and cytotoxicity from reactive oxygen species. Proc. Natl. Acad. Sci. USA 90 (1993) 9813-9817
57. Wong C.M., Zhou Y., Ng R.W., Kung Hf H.F., and Jin D.Y. Cooperation of yeast peroxiredoxins Tsa1p and Tsa2p in the cellular defense against oxidative and nitrosative stress. J. Biol. Chem. 277 (2002) 5385-5394
58. Woo H.A., Kang S.W., Kim H.K., Yang K.S., Chae H.Z., and Rhee S.G. Reversible oxidation of the active site cysteine of peroxiredoxins to cysteine sulfinic acid. Immunoblot detection with antibodies specific for the hyperoxidized cysteine-containing sequence. J. Biol. Chem. 278 (2003) 47361-47364
59. Wood Z.A., Poole L.B., and Karplus P.A. Peroxiredoxin evolution and the regulation of hydrogen peroxide signaling. Science 300 (2003) 650-653
60. Wood Z.A., Schroder E., Robin Harris J., and Poole L.B. Structure, mechanism and regulation of peroxiredoxins. Trends Biochem. Sci. 28 (2003) 32-40