ESR detection of intraphagosomal superoxide in polymorphonuclear leukocytes using 5-(diethoxyphosphoryl)-5-methyl-1-pyrroline-N-oxide

References

• Barber M.J., Rosen G.M., Siegel L.M., Rauckman E.J. Evidence for formation of superoxide and formate radicals in Methanobacterium formicicum. Journal of Bacteriology 1983; 153: 1282–1286
   PubMedGoogle Scholar
• Babior B.M., Kipnes R.S., Curnutte J.T. Biological defense mechanisms. The production by leukocytes of superoxide, a potential bactericidal agent. Journal of Clinical Investigation 1973; 52: 741–744
   PubMed Web of Science ®Google Scholar
• Bogomolski-Yahalom V., Matzner Y. Disorders of neutrophil function. Blood Review 1995; 9: 183–190
   PubMed Web of Science ®Google Scholar
• Bokoch G.M. Chemoattractant signaling and leukocyte activation. Blood 1995; 86: 1649–1660
   PubMed Web of Science ®Google Scholar
• Segal A.W. The NADPH oxidase and chronic granulomatous disease. Molecular medicine Today 1996; 2: 129–135
   PubMedGoogle Scholar
• Inanami O., Johnson J.L., McAdara J.K., Benna J.E.L., Faust L.P., Newburger P.E., Babior B.M. Activation of the leukocyte NADPH oxidase by phorbol ester requires the phosphorylation of p47PHOX on serine 303 or 304. Journal of Biological Chemistry 1998; 273: 9539–9543
   PubMed Web of Science ®Google Scholar
• Inanami O., Johnson J.L., Babior B.M. The leukocyte NADPH oxidase subunit p47PHOX: the role of the cysteine residues. Archives of Biochemistry and Biophysics 1998; 350: 36–40
   PubMed Web of Science ®Google Scholar
• Yamamori T., Inanami O., Nagahata H., Cui Y.D., Kuwabara M. Roles of p38 MAPK, PKC and PI3-K in the signaling pathways of NADPH oxidase activation and phagocytosis in bovine polymorphonuclear leukocytes. FEBS Letters 2000; 467: 253–258
   PubMed Web of Science ®Google Scholar
• Ambruso D.R., Johnston R.B., Jr. Lactoferrin enhances hydroxyl radical production by human neutrophils, neutrophil particulate fractions, and an enzymatic generating system. Journal of Clinical Investigation 1981; 67: 353–360
   Google Scholar
• Ohno Y., Hirai K., Kanoh T., Uchino H., Ogawa K. Subcellular localization of H2O2 production in human neutrophils stimulated with particles and an effect of cytochalasin-B on the cells. Blood 1982; 60: 253–260
   PubMed Web of Science ®Google Scholar
• Bellavite P., Serra M.C., Davoli A., Rossi F. Selective enrichment of NADPH oxidase activity in phagosomes from guinea pig polymorphonuclear leukocytes. Inflammation 1982; 6: 21–29
   PubMedGoogle Scholar
• Briggs R.T., Drath D.B., Karnovsky M.L., Karnovsky M.J. Localization of NADH oxidase on the surface of human polymorphonuclear leukocytes by a new cytochemical method. Journal of Cell Biology 1975; 67: 566–586
   PubMed Web of Science ®Google Scholar
• Woodman R.C., Ruedi J.M., Jesaitis A.J., Okamura N., Quinn M.T., Smith R.M., Curnutte J.T., Babior B.M. Respiratory burst oxidase and three of four oxidase-related polypeptides are associated with the cytoskeleton of human neutrophils. Journal of Clinical Investigation 1991; 87: 1345–1351
   PubMed Web of Science ®Google Scholar
• Berton G., Bellavite P., de-Nicola G., Dri P., Rossi F. Plasma membrane and phagosome localisation of the activated NADPH oxidase in elicited peritoneal macrophages of the guinea-pig. Journal of Pathology 1982; 136: 241–252
   PubMedGoogle Scholar
• Jiang X., Kobayashi T., Nahirney P.C., Saz E.G.D., Seguchi H. Ultracytochemical study on the localization of superoxide producing sites in stimulated rat neutrophils. Anatomical Record 2000; 258: 156–165
   PubMedGoogle Scholar
• Kobayashi T., Robinson J.M., Seguchi H. Identification of intracellular sites of superoxide production in stimulated neutrophils. Journal of Cell Science 1998; 111: 81–91
   PubMed Web of Science ®Google Scholar
• Britigan B.E., Cohen M.S., Rosen G.M. Detection of the production of oxygen-centered free radicals by human neutrophils using spin trapping techniques: a critical perspective. Journal of Leukocyte Biology 1987; 41: 349–362
   PubMed Web of Science ®Google Scholar
• Britigan B.E., Rosen G.M., Chai Y., Cohen M.S. Do human neutrophils make hydroxyl radical? Determination of free radicals generated by human neutrophils activated with a soluble or particulate stimulus using electron paramagnetic resonance spectrometry. Journal of Biological Chemistry 1986; 261: 4426–4431
   PubMed Web of Science ®Google Scholar
• Britigan B.E., Rosen G.M., Thompson B.Y., Chai Y., Cohen M.S. Stimulated human neutrophils limit iron-catalyzed hydroxyl radical formation as detected by spin-trapping techniques. Journal of Biological Chemistry 1986; 261: 17026–17032
   PubMed Web of Science ®Google Scholar
• Kuwabara M., Nishimura Y., Sato F., Takahashi T.A., Tajima M., Takahashi K., Nagahata H. Spin-trapping and chemiluminescence studies of neutrophils from a Holstein-Friesian calf with bovine leukocyte adhesion deficiency. Free Radical Research Communications 1993; 18: 309–318
   PubMed Web of Science ®Google Scholar
• Pou S., Rosen G.M., Britigan B.E., Cohen M.S. Intracellular spin-trapping of oxygen-centered radicals generated by human neutrophils. Biochimica and Biophysica Acta 1989; 991: 459–464
   PubMedGoogle Scholar
• Kotake Y., Reinke L.A., Tanigawa T., Koshida H. Determination of the rate of superoxide generation from biological systems by spin trapping: use of rapid oxygen depletion to measure the decay rate of spin adducts. Free Radical Biology and Medicine 1994; 17: 215–223
   PubMed Web of Science ®Google Scholar
• Kleinhanse F.W., Barefoot S.T. Spin trap determination of free radical burst kinetics in stimulated neutrophils. Journal of Biological Chemistry 1987; 262: 12452–12457
   PubMedGoogle Scholar
• Finkelstein E., Rosen G.M., Rauckman E.J. Production of hydroxyl radical by decomposition of superoxide spin-trapped adducts. Molecular Pharmacology 1982; 21: 262–265
   PubMed Web of Science ®Google Scholar
• Frejaville C., Karoui H., Tuccio B., Le Moigne F., Culcasi M., Pietri S., Lauricella R., Tordo P. 5-Diethyoxyphosphoryl-5-methyl-1-pyrroline N-Oxide (DEPMPO): a New Phosphorylated Nitrone for the efficient In Vitro and In Vivo Spin Trapping of Oxygen-centred Radicals. Journal of Chemical Society, Chemical Communications 1994; 15: 1793–1794
   Google Scholar
• Frejaville C., Karoui H., Tuccio B., Le Moigne F., Culcasi M., Pietri S., Lauricella R., Tordo P. 5-(Diethoxyphosphoryl)-5-methyl-1-pyrroline N-oxide: a new efficient phosphorylated nitrone for the in vitro and in vivo spin trapping of oxygen-centered radicals. Journal of Medical Chemistry 1995; 38: 258–265
   PubMed Web of Science ®Google Scholar
• Roubaud V., Sankarapandi S., Kuppusamy P., Tordo P., Zweier J.L. Quantitative measurement of superoxide generation and oxygen consumption from leukocytes using electron paramagnetic resonance spectroscopy. Analitical Biochemistry 1998; 247: 210–217
   Google Scholar
• Chamulitrat W. Activation of the superoxide-generating NADPH oxidase of intestinal lymphocytes produces highly reactive free radicals from sulfite. Free Radical Biology and Medicine 1999; 27: 411–421
   PubMed Web of Science ®Google Scholar
• Samuni A., Carmichael A.J., Russo A., Mitchell J.B., Riesz P. On the spin trapping and ESR detection of oxygen-derived radicals generated inside cells. Proceedings of the National Academy of Sciences of the U.S.A. 1986; 83: 7593–7597
   PubMed Web of Science ®Google Scholar
• Timmins G.S., Liu K.J., Bechara E.J.H., Kotake Y., Swartz H.M. Trapping of free radicals with direct in vivo EPR detection: a comparison of 5,5-dimethyl-1-pyrroline-N-oxide and 5-diethoxyphosphoryl-5-methyl-1-pyrroline-N-oxide as spin traps for HO· and SO4-. Free Radical Biology and Medicine 1999; 27: 329–333
   PubMed Web of Science ®Google Scholar
• Kuwabara M., Nagahata H., Takahashi T.A., Inanami O. Spin-trapping detection of superoxides in polymorphonuclear leukocytes stimulated with serum-opsonized zymosan. Japanese Journal of Veterinary Research 2000; 48: 3–13
   PubMedGoogle Scholar