Spin Trapping of Superoxide from Glass Adherent Polymorphonuclear Leukocytes Induced by N-Formylmethionyl-Leucyl-Phenylalanine

References

• Anderson B. O., Brown J. M., Harken A. H. Mechanisms of neutrophil-mediated tissue injury. Journal of Surgical Research 1991; 51: 170–179, 1991
   PubMed Web of Science ®Google Scholar
• Fehr J., Moser R., Leppert D., Groscurth P. Anti-adhesive properties of biological surfaces are protective against stimulated granulocytes. Journal of Clinical Investigation 1985; 76: 535–542
   PubMed Web of Science ®Google Scholar
• Nathan G. F. Neutrophil activation on biological surfaces. Massive secretion of hydrogen peroxide in response to products of macrophages and lymphocytes. Journal of Clinical Investigation 1987; 80: 1550–1560
   PubMed Web of Science ®Google Scholar
• Nathan G. F. Respiratory burst in adherent human neutrophils: Triggering by colony-stimulation factors CSF-GM and CSF-G. Blood 1989; 73: 301–306
   PubMed Web of Science ®Google Scholar
• Shappel S. B., Toman C., Anderson D. C., Taylor A. A., Entman M. L., Smith C. W. Mac-1 (CD11b/CD18) mediates adherence-dependent hydrogen peroxide production by human and canine neutrophils. Journal of Immunology 1990; 144: 2702–2711
   PubMedGoogle 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
• Ferrante A., Thong Y. H. Separation of mononuclear and polymorphonuclear leukocytes from human blood by one-step Hypaque-Ficoll method is dependent on blood column height. Journal of Immunological Methods 1982; 48: 81–85
   PubMed Web of Science ®Google Scholar
• Green M. R., Hill H. A.O., Okolow-Zubkowska M. J., Segal A. W. The production of hydroxyl and superoxide radicals by stimulated human neutrophils-Measarements by EPR spec-troscopy. FEBS Letters 1979; 100: 23–26
   PubMed Web of Science ®Google Scholar
• Aida Y., Pabst M. J. Neutrophil responses to lipopolysaccharide. Effect of adherence on triggering and priming of the respiratory burst. Journal of Immunology 1991; 146: 1271–1276
   PubMed Web of Science ®Google Scholar
• Britigan B. E., Rosen G. M., Chai Y., Cohen M. S. Do human neutrophils make hydroxyl radical?. Journal of Biological Chemistry 1986; 261: 4426–4431
   PubMed Web of Science ®Google Scholar
• Samuni A., Black C. D.V., Krishna G. M., Malech H. L., Bernstein E. F., Russo A. A Hydroxyl radical production by stimulated neutrophils reappraised. Journal of Biological Chemistry 1988; 263: 13797–13801
   PubMed Web of Science ®Google Scholar
• Dahinden C. A., Fehr J., Hugle T. E. Role of cell surface contact in the kinetics of superoxide production by granulocytes. Journal of Clinical Investigation 1983; 72: 113–121
   PubMed Web of Science ®Google Scholar
• Neuman M., Kownatzki E. The effect of adherence on the generation of reactive oxygen species by human neutrophilic granulocytes. Agents and Actions 1989; 26: 183–185
   PubMedGoogle Scholar
• Hoffstein S. T., Gennaro D. E., Manzi R. M. Surface contact inhibits neutrophil superoxide generation induced by soluble stimuli. Laboratory Investigation 1985; 52: 515–522
   PubMed Web of Science ®Google Scholar
• Rebut-Bonneton C., Bailly S., Pasquier C. Superoxide anion production in glass-adherent polymorphonuclear leukocytes and its relationship to calcium movement. Journal of Leukocyte Biology 1988; 44: 402–410
   PubMed Web of Science ®Google Scholar
• Laurent F., Benoliel A. M., Capo C., Bongrand P. Oxidative metabolism of polymorphonuclear leukocytes: modulation by adhesive stimuli. Journal of Leukocyte Biology 1991; 49: 217–226
   PubMed Web of Science ®Google Scholar
• Tanigawa T., Kotake Y., Reinke L. A. 1993, manuscript in preparation
   Google Scholar
• Albelda S., Buck C. Integrins and other cell adhesion molecules. FASEB Journal 1990; 4: 2868–2880
   PubMed Web of Science ®Google Scholar
• Todd R. F., III, Arnaut M. A., Rosen R. E., Crowly C. A., Peter W. A., Babior B. M. Subcellular localization of the large subunit of Mol (Molα; formerly gp110), a surface glycoprotein associated with neutrophil adhesion. Journal of Clinical Investigation 1984; 74: 1280–1290
   PubMed Web of Science ®Google Scholar
• Philips M. R., Buyon J. P., Winchester R., Weissmann G., Abramson S. B. Up-regulation of the iC3b receptor (CR3) is neither necessary nor sufficient to promote neutrophil aggregation. Journal of Clinical Investigation 1988; 82: 495–501
   PubMed Web of Science ®Google Scholar
• Schleiffenbaum B., Moser R., Patarroyo M., Fehr J. The cell surface glycoprotein Mac-1 (CD11b/CD18) mediates neutrophil adhesion and modulates degranulation independently of its quantitative cell surface expression. Journal of Immunology 1989; 142: 3537–3545
   PubMed Web of Science ®Google Scholar
• Fehr J., Dahinden C. Modulating influence of chemotactic factor-induced cell adhesiveness on granulocyte function. Journal of Clinical Investigation 1979; 64: 8–16
   PubMed Web of Science ®Google Scholar
• Southwick F. S., Dabiri G. A., Paschetto M., Zigmond S. H. Polymorphonuclear leukocyte adherence induces actin polymerization by transduction pathway which differs from that used by chemoattractants. Journal of Cell Biology 1989; 109: 1561–1569
   PubMed Web of Science ®Google Scholar
• Howard T. H., Oresajo C. O. The kinetics of chemotactic peptide-induced change in Factin content, F-actin distribution, and the shape of neutrophils. Journal of Cell Biology 1985; 101: 1078–1085
   PubMedGoogle Scholar
• Jesaitis A. J., Tolley J. O., Allen R. A. Receptor-cytoskeleton interactions and membrane traffic may regulate chemoattractant-induced superoxide production in human granulocytes. Journal of Biological Chemistry 1986; 261: 13662–13669
   PubMed Web of Science ®Google Scholar
• Woodman R. C., Ruedi J. M., Jesaitis A. J., Okamura N., Quinn M. T., Smith R. M. Curnutte 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
• Nathan C., Srimal S., Farber C., Sanchez E., Kabbash L., Asch A., Gailit J., Wright S. D. Cytokine-induced respiratory burst of human neutrophils: Dependence on extracellular matrix proteins and CD11/CD18 integrins. Journal of Cell Biology 1989; 109: 1341–1349
   PubMed Web of Science ®Google Scholar
• Docampo R., Casellas A. M., Madeira E. D., Cardoni R. L., Moreno S. N.J., Mason R. P. Oxygen-derived radicals from Trypanosoma cruzi-stimulated human neutrophils. FEBS Letters 1983; 155: 25–30
   PubMedGoogle 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: effect of temperature and cellular metabolism. Journal of Biological Chemistry 1986; 261: 17026–17032
   PubMed Web of Science ®Google Scholar
• Rosen G. M., Britigan B. E., Cohen M. S., Ellington S. P., Barber M. J. Detection of phagocyte-derived free radicals with spin trapping techniques: effect of temperature and cellular metabolism. Biochimica Biophysics Acta 1988; 969: 236–241
   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 Biophysica Acta 1989; 991: 459–464
   PubMedGoogle Scholar
• Pou S., Cohen M. S., Britigan B. E., Rosen G. M. Spin-trapping and human neutrophils. Limits of detection of hydroxyl radical. Journal of Biological Chemistry 1989; 264: 12299–12302
   PubMed Web of Science ®Google Scholar
• Britigan B. E., Hamill D. R. The interaction of 5,5-dimethyl-1-pyrroline-N-oxide with human myeloperoxidase and its potential impact on spin trapping of neutrophil-derived free radicals. Archives of Biochemistry and Biophysics 1989; 175: 72–81
   Google Scholar
• Britigan B. E., Hassett D. J., Rosen G. M., Hamill D. R., Cohen M. S. Neutrophil degranulation inhibits potential hydroxyl-radical formation. Relative impact of myeloperoxidase and lactoferrin release on hydroxyl-radical production by iron-supplemented neutrophils assessed by spin-trapping techniques. Biochemical Journal 1989; 264: 447–455
   PubMedGoogle Scholar
• Britigan B. E., Hamill D. R. Effect of the spin trap 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) on human neutrophil function: Novel inhibition of neutrophil stimulus-response coupling?. Free Radical Biology and Medicine 1990; 8: 459–470
   PubMedGoogle Scholar
• Cohen M. S., Britigan B. E., Chai Y. S., Pou S., Roeder T. L., Rosen G. M. Phagocyte-derived free radicals stimulated by ingestion of iron-rich Staphylococcus aureus: A spin-trapping study. Journal of Infectious Diseases 1991; 163: 819–824
   PubMedGoogle Scholar
• Ramos C. L., Pou S., Britigan B. E., Cohen M. S., Rosen G. M. Spin trapping evidence for myeloperoxidase-dependent hydroxyl radical formation by human neutrophils and monocytes. Journal of Biological Chemistry 1992; 267: 8307–8312
   PubMed Web of Science ®Google Scholar
• Ueno I., Kohno M., Mitsuta K., Mizuta Y., Kanegasaki S. S. Reevaluation of the spin-trapped adduct formed from 5,5-dimethyl-1-pyrroline-1-oxide during the respiratory burst in neutrophils. Journal of Biochemistry 1989; 105: 905–910
   PubMed Web of Science ®Google Scholar
• Samuni A., Samuni A., Swartz H. M. The cellular-induced decay of DMPO spin adducts of .OH and .O2-. Free Radical Biology and Medicine 1989; 6: 179–183
   PubMed Web of Science ®Google Scholar
• Samuni A., Krishna M., Reisz P., Finkelstein E., Russo A. Superoxide reaction with nitroxide spin-adducts. Free Radical Biology and Medicine 1989; 6: 141–148
   PubMed Web of Science ®Google Scholar
• Black C. D.V., Cook J. A., Russo A., Samuni A. Superoxide production by stimulated neutrophils: temperature effect. Free Radical Research Communications 1991; 12–13: 27–37
   Google Scholar
• Hume D. A., Gordon S., Thornalley P. J., Bannister J. V. The production of oxygen-centered radicals by Bacillus-Calmette-Guerin-activated macrophages. Biochimica Biophysica Acta 1983; 763: 245–250
   PubMed Web of Science ®Google Scholar