In vivo imaging of reactive oxygen and nitrogen species in inflammation using the luminescent probe L-012

Free Radical Biology and Medicine

Volumn 47, Issue 6, 2009, Pages 760-766

  Kielland, Anders ^a   Blom, Thomas ^b   Nandakumar, Kutty Selva ^b   Holmdahl, Rikard ^b   Blomhoff, Rune ^a   Carlsen, Harald ^a  

^a UNIVERSITY OF OSLO   (Norway)

^b LUND UNIVERSITY   (Sweden)

Author keywords

Chemiluminescence; Free radical; In vivo; Inflammation; L 012; Luminescence; Molecular imaging; Mouse; Optical imaging; RNS; ROS

Indexed keywords

REACTIVE NITROGEN SPECIES; REACTIVE OXYGEN METABOLITE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE 2;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTHRITIS; ARTICLE; CHEMOLUMINESCENCE; CONTROLLED STUDY; GENE MUTATION; IN VIVO STUDY; INFLAMMATION; MOLECULAR IMAGING; MOUSE; NONHUMAN; OTITIS; PRIORITY JOURNAL;

ACETOPHENONES; ANIMALS; CYCLIC N-OXIDES; DIAGNOSTIC IMAGING; INFLAMMATION; LUMINESCENT AGENTS; LUMINOL; MICE; NADPH OXIDASE; NG-NITROARGININE METHYL ESTER; NITRIC OXIDE SYNTHASE; OXIDATIVE STRESS; REACTIVE NITROGEN SPECIES; REACTIVE OXYGEN SPECIES; SENSITIVITY AND SPECIFICITY; SPIN LABELS; SUPEROXIDE DISMUTASE;

ANIMALIA; MUS;

EID: 68549128495     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2009.06.013     Document Type: Article

References (43)

1. McCord J.M. The evolution of free radicals and oxidative stress. Am. J. Med. 108 (2000) 652-659
2. Jackson M.J., Papa S., Bolanos J., Bruckdorfer R., Carlsen H., Elliott R.M., Flier J., Griffiths H.R., Heales S., Holst B., Lorusso M., Lund E., Oivind Moskaug J., Moser U., Di Paola M., Polidori M.C., Signorile A., Stahl W., Vina-Ribes J., and Astley S.B. Antioxidants, reactive oxygen and nitrogen species, gene induction and mitochondrial function. Mol. Aspects Med. 23 (2002) 209-285
3. Reeves E.P., Lu H., Jacobs H.L., Messina C.G., Bolsover S., Gabella G., Potma E.O., Warley A., Roes J., and Segal A.W. Killing activity of neutrophils is mediated through activation of proteases by K+flux. Nature 416 (2002) 291-297
4. Segal A.W., Geisow M., Garcia R., Harper A., and Miller R. The respiratory burst of phagocytic cells is associated with a rise in vacuolar pH. Nature 290 (1981) 406-409
5. Valko M., Leibfritz D., Moncol J., Cronin M.T., Mazur M., and Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int. J. Biochem. Cell Biol. 39 (2007) 44-84
6. Kumar A., Wu H., Collier-Hyams L.S., Hansen J.M., Li T., Yamoah K., Pan Z.Q., Jones D.P., and Neish A.S. Commensal bacteria modulate cullin-dependent signaling via generation of reactive oxygen species. EMBO J. 26 (2007) 4457-4466
7. Yao H., Yang S.R., Kode A., Rajendrasozhan S., Caito S., Adenuga D., Henry R., Edirisinghe I., and Rahman I. Redox regulation of lung inflammation: role of NADPH oxidase and NF-kappaB signalling. Biochem. Soc. Trans. 35 (2007) 1151-1155
8. Fialkow L., Wang Y., and Downey G.P. Reactive oxygen and nitrogen species as signaling molecules regulating neutrophil function. Free Radic. Biol. Med. 42 (2007) 153-164
9. Gelderman K.A., Hultqvist M., Pizzolla A., Zhao M., Nandakumar K.S., Mattsson R., and Holmdahl R. Macrophages suppress T cell responses and arthritis development in mice by producing reactive oxygen species. J. Clin. Invest. 117 (2007) 3020-3028
10. Gelderman K.A., Hultqvist M., Holmberg J., Olofsson P., and Holmdahl R. T cell surface redox levels determine T cell reactivity and arthritis susceptibility. Proc. Natl. Acad. Sci. U.S.A. 103 (2006) 12831-12836
11. Gelderman K.A., Hultqvist M., Olsson L.M., Bauer K., Pizzolla A., Olofsson P., and Holmdahl R. Rheumatoid arthritis: the role of reactive oxygen species in disease development and therapeutic strategies. Antioxid. Redox Signal. 9 (2007) 1541-1567
12. Olofsson P., Holmberg J., Tordsson J., Lu S., Akerstrom B., and Holmdahl R. Positional identification of Ncf1 as a gene that regulates arthritis severity in rats. Nat. Genet. 33 (2003) 25-32
13. Halliwell B., and Whiteman M. Measuring reactive species and oxidative damage in vivo and in cell culture: how should you do it and what do the results mean?. Br. J. Pharmacol. 142 (2004) 231-255
14. Videla L.A., Correa L., Rivera M., and Sir T. Zymosan-induced luminol-amplified chemiluminescence of whole blood phagocytes in experimental and human hyperthyroidism. Free Radic. Biol. Med. 14 (1993) 669-675
15. Van Dyke K., Patel S., and Vallyathan V. Lucigenin chemiluminescence assay as an adjunctive tool for assessment of various stages of inflammation: a study of quiescent inflammatory cells. J. Biosci. 28 (2003) 115-119
16. Lucas M., and Solano F. Coelenterazine is a superoxide anion-sensitive chemiluminescent probe: its usefulness in the assay of respiratory burst in neutrophils. Anal. Biochem. 206 (1992) 273-277
17. Wardman P. Fluorescent and luminescent probes for measurement of oxidative and nitrosative species in cells and tissues: progress, pitfalls, and prospects. Free Radic. Biol. Med. 43 (2007) 995-1022
18. Chen W.T., Tung C.H., and Weissleder R. Imaging reactive oxygen species in arthritis. Mol. Imaging 3 (2004) 159-162
19. Nishinaka Y., Aramaki Y., Yoshida H., Masuya H., Sugawara T., and Ichimori Y. A new sensitive chemiluminescence probe, L-012, for measuring the production of superoxide anion by cells. Biochem. Biophys. Res. Commun. 193 (1993) 554-559
20. Imada I., Sato E.F., Miyamoto M., Ichimori Y., Minamiyama Y., Konaka R., and Inoue M. Analysis of reactive oxygen species generated by neutrophils using a chemiluminescence probe L-012. Anal. Biochem. 271 (1999) 53-58
21. Daiber A., Oelze M., August M., Wendt M., Sydow K., Wieboldt H., Kleschyov A.L., and Munzel T. Detection of superoxide and peroxynitrite in model systems and mitochondria by the luminol analogue L-012. Free Radic. Res. 38 (2004) 259-269
22. Daiber A., August M., Baldus S., Wendt M., Oelze M., Sydow K., Kleschyov A.L., and Munzel T. Measurement of NAD(P)H oxidase-derived superoxide with the luminol analogue L-012. Free Radic. Biol. Med. 36 (2004) 101-111
23. Massoud T.F., and Gambhir S.S. Molecular imaging in living subjects: seeing fundamental biological processes in a new light. Genes. Dev. 17 (2003) 545-580
24. Carlsen H., Moskaug J.O., Fromm S.H., and Blomhoff R. In vivo imaging of NF-kappa B activity. J. Immunol. 168 (2002) 1441-1446
25. Hultqvist M., Olofsson P., Holmberg J., Backstrom B.T., Tordsson J., and Holmdahl R. Enhanced autoimmunity, arthritis, and encephalomyelitis in mice with a reduced oxidative burst due to a mutation in the Ncf1 gene. Proc. Natl. Acad. Sci. USA 101 (2004) 12646-12651
26. Park H.S., Jung H.Y., Park E.Y., Kim J., Lee W.J., and Bae Y.S. Cutting edge: direct interaction of TLR4 with NAD(P)H oxidase 4 isozyme is essential for lipopolysaccharide-induced production of reactive oxygen species and activation of NF-kappa B. J. Immunol. 173 (2004) 3589-3593
27. Pozsgai G., Sandor K., Perkecz A., Szolcsanyi J., Helyes Z., Brain S.D., and Pinter E. Topical acetone treatment induces neurogenic oedema on the sensitized mouse ear: an in vivo study using transient receptor potential vanilloid 1 (TRPV1) receptor knockout mice. Inflamm. Res. 56 (2007) 459-467
28. Nandakumar K.S., and Holmdahl R. Efficient promotion of collagen antibody induced arthritis (CAIA) using four monoclonal antibodies specific for the major epitopes recognized in both collagen induced arthritis and rheumatoid arthritis. J. Immunol. Methods 304 (2005) 126-136
29. Henderson R.B., Hobbs J.A., Mathies M., and Hogg N. Rapid recruitment of inflammatory monocytes is independent of neutrophil migration. Blood 102 (2003) 328-335
30. Miletic A.V., Graham D.B., Montgrain V., Fujikawa K., Kloeppel T., Brim K., Weaver B., Schreiber R., Xavier R., and Swat W. Vav proteins control MyD88-dependent oxidative burst. Blood 109 (2007) 3360-3368
31. Nandakumar K.S., Backlund J., Vestberg M., and Holmdahl R. Collagen type II (CII)-specific antibodies induce arthritis in the absence of T or B cells but the arthritis progression is enhanced by CII-reactive T cells. Arthritis Res. Ther. 6 (2004) R544-R550
32. Sohn H.Y., Gloe T., Keller M., Schoenafinger K., and Pohl U. Sensitive superoxide detection in vascular cells by the new chemiluminescence dye L-012. J. Vasc. Res. 36 (1999) 456-464
33. Hahn S.M., Tochner Z., Krishna C.M., Glass J., Wilson L., Samuni A., Sprague M., Venzon D., Glatstein E., Mitchell J.B., et al. Tempol, a stable free radical, is a novel murine radiation protector. Cancer Res. 52 (1992) 1750-1753
34. Ximenes V.F., Kanegae M.P., Rissato S.R., and Galhiane M.S. The oxidation of apocynin catalyzed by myeloperoxidase: proposal for NADPH oxidase inhibition. Arch. Biochem. Biophys. 457 (2007) 134-141
35. Werner C.G., Godfrey V., Arnold R.R., Featherstone G.L., Bender D., Schlossmann J., Schiemann M., Hofmann F., and Pryzwansky K.B. Neutrophil dysfunction in guanosine 3′,5′-cyclic monophosphate-dependent protein kinase I-deficient mice. J. Immunol. 175 (2005) 1919-1929
36. Rickinger O., Sheriff H., and Hirschelmann R. Effects of (D-Ala2)methionine enkephalinamide in PMA-induced mouse ear edema. Agents Actions 41 (1994) 118-119
37. Ii M., Yoshida H., Aramaki Y., Masuya H., Hada T., Terada M., Hatanaka M., and Ichimori Y. Improved enzyme immunoassay for human basic fibroblast growth factor using a new enhanced chemiluminescence system. Biochem. Biophys. Res. Commun. 193 (1993) 540-545
38. Bedard K., and Krause K.H. The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiol. Rev. 87 (2007) 245-313
39. Huycke M.M., Abrams V., and Moore D.R. Enterococcus faecalis produces extracellular superoxide and hydrogen peroxide that damages colonic epithelial cell DNA. Carcinogenesis 23 (2002) 529-536
40. Soesatyo M., Biewenga J., Kraal G., and Sminia T. The localization of macrophage subsets and dendritic cells in the gastrointestinal tract of the mouse with special reference to the presence of high endothelial venules. An immuno-and enzyme-histochemical study. Cell Tissue Res. 259 (1990) 587-593
41. Kunisawa J., Takahashi I., and Kiyono H. Intraepithelial lymphocytes: their shared and divergent immunological behaviors in the small and large intestine. Immunol. Rev. 215 (2007) 136-153
42. Sanders L.M., Henderson C.E., Hong M.Y., Barhoumi R., Burghardt R.C., Carroll R.J., Turner N.D., Chapkin R.S., and Lupton J.R. Pro-oxidant environment of the colon compared to the small intestine may contribute to greater cancer susceptibility. Cancer Lett. 208 (2004) 155-161
43. Samuni A., Krishna C.M., Cook J., Black C.D., and Russo A. On radical production by PMA-stimulated neutrophils as monitored by luminol-amplified chemiluminescence. Free Radic. Biol. Med. 10 (1991) 305-313