Superoxide release is involved in membrane potential changes in mouse peritoneal macrophages

Free Radical Biology and Medicine

Volumn 24, Issue 1, 1998, Pages 168-174

  Gamaley, Irene A ^a   Kirpichnikova, Ksenia M ^a   Klyubin, Igor V ^a  

^a INSTITUTE OF CYTOLOGY   (Russian Federation)

Author keywords

Chemiluminescence; Free radicals; Intracellular Ca2+; K+ channels; Membrane potential; Oxonol dye; Superoxide

Indexed keywords

CALCIUM ION; CATALASE; FORMYLMETHIONYLLEUCYLPHENYLALANINE; GAMMA INTERFERON; LIPOPOLYSACCHARIDE; POTASSIUM ION; QUINIDINE; REACTIVE OXYGEN METABOLITE; SUPEROXIDE; SUPEROXIDE DISMUTASE; THROMBOCYTE ACTIVATING FACTOR; XANTHINE; XANTHINE OXIDASE;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CELL MEMBRANE DEPOLARIZATION; CELL MEMBRANE POTENTIAL; CHEMOLUMINESCENCE; CONTROLLED STUDY; HYPERPOLARIZATION; MOUSE; NONHUMAN; PERITONEUM MACROPHAGE; POTASSIUM CELL LEVEL; PRIORITY JOURNAL;

ANIMALS; CHEMILUMINESCENT MEASUREMENTS; MACROPHAGES, PERITONEAL; MEMBRANE POTENTIALS; MICE; N-FORMYLMETHIONINE LEUCYL-PHENYLALANINE; PLATELET ACTIVATING FACTOR; REACTIVE OXYGEN SPECIES; RESPIRATORY BURST; SUPEROXIDES;

ANIMALIA;

EID: 0031983383     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0891-5849(97)00212-8     Document Type: Article

References (52)

1. Morel F., Doussiere J., Vignais P. V. The superoxide-generating oxidase of phagocytic cells. Physiological, molecular and pathological aspects. Eur. J. Biochem. 201:1991;523-546.
2. Thelen M., Dewald B., Baggiolini M. Neutrophil signal transduction and activation of the respiratory burst. Physiol. Rev. 73:1993;797-821.
3. Schreck R., Rieber P., Baeuerle P. A. Reactive oxygen intermediates as apparently widely used messengers in the activation of the NF-kappa B transcription factor and HIV-1. EMBO J. 10:1991;2247-2258.
4. 2 for platelet-derived growth factor signal transduction. Science. 270:1995;296-299.
5. DelBuono B. J., Simons E. R. Role of the plasma membrane in signal transduction in human polymorphonuclear leukocytes. J. Cell. Physiol. 154:1993;80-91.
6. 4 induce hyperpolarization of human endothelial cells but depolarization of neutrophils. Biochem. Biophys. Res. Commun. 153:1988;805-810.
7. Holevinsky K. O., Nelson D. J. Simultaneous detection of free radical release and membrane current during phagocytosis. J. Biol. Chem. 270:1995;8328-8336.
8. Ahlin A., Gyllenhammar H., Ringertz B., Palmblad J. Neutrophil membrane potential changes and homotypic aggregation kinetics are pH-dependent: studies of chronic granulomatous disease. J. Lab. Clin. Med. 125:1995;392-401.
9. Seeds M. C., Parce J. W., Szejda P., Bass D. A. Independent stimulation of membrane potential changes and the oxidative metabolic burst in polymorphonuclear leukocytes. Blood. 65:1985;233-240.
10. + channels in N1E-115 neuroblastoma cells by platelet-activating factor. Biochem. Biophys. Res. Commun. 218:1996;745-748.
11. + movements in the membrane signal induced by PAF-acether. Biochem. Pharmacol. 35:1986;2811-2815.
12. Sullivan R., Melnick D. A., Malech H. L., Meshulam T., Simons E. R., Lazzari K. G., Proto P. J., Gadenne A. S., Leavitt J. L., Griffin J. D. The effects of phorbol myristate acetate and chemotactic peptide on transmembrane potentials and cytosolic free calcium in mature granulocytes evolve sequentially as the cells differentiate. J. Biol. Chem. 262:1987;1274-1281.
13. Lazzari K. G., Proto P., Simons E. R. Neutrophil hyperpolarization in response to a chemotactic peptide. J. Biol. Chem. 265:1990;10959-10967.
14. Gamaley I. A., Kirpichnikova K. M., Klyubin I. V. Activation of murine macrophages by hydrogen peroxide. Cell. Signal. 6:1994;949-957.
15. Jones G. S., VanDyke K., Castranova V. Transmembrane potential changes associated with superoxide release from human granulocytes. J. Cell. Physiol. 106:1981;75-83.
16. 2+ and in membrane potential of human neutrophils. J. Biol. Chem. 261:1986;9710-9713.
17. Jones O. T. G. The regulation of superoxide production by the NADPH oxidase of neutrophils and other mammalian cells. BioEssays. 16:1994;919-923.
18. 2 induced hyperpolarization of pancreatic B-cells. Pflugers Arch. 426:1994;552-554.
19. i of cultured rat arterial smooth muscle cells. Biochem. Biophys. Res. Commun. 209:1995;139-145.
20. Franceschi D., Graham D., Sarasua M., Zollinger R. M. Jr. Mechanisms of oxygen free radical-induced calcium overload in endothelial cells. Surgery. 108:1990;292-297.
21. Gamaley I. A., Kaulin A. B., Kirpichnikova K. M. Macrophage membrane potential described by oxonol dye fluorescence measurements. Tsitologia. 33:1991;60-66.
22. Scott J. A., Rabito C. A. Oxygen radicals and plasma membrane potential. Free Rad. Biol. Med. 5:1988;237-246.
23. Randriamampita C., Trautmann A. Ionic channels in murine macrophages. J. Cell Biol. 105:1987;761-769.
24. 2+-sensitive potassium channels described by oxonol dye fluorescence measurements. J. Cell. Physiol. 125:1985;72-81.
25. Seligmann B. E., Gallin J. I. Comparison of indirect probes of membrane potential utilized in studies of human neutrophils. J. Cell. Physiol. 115:1983;105-115.
26. + conducting channel. Biochem. J. 251:1987;563-567.
27. Demaurex N., Schrenzel J., Jaconi M. E., Lew D. P., Krause K. H. Proton channels, plasma membrane potential, and respiratory burst in human neutrophils. Eur. J. Haematol. 51:1993;309-312.
28. Seligmann B. S., Gallin E. K., Martin D. L., Shain W., Gallin J. I. Interaction of chemotactic factors with human polymorphonuclear leukocytes: Studies using a membrane-potential sensitive cyanine dye. J. Membrane Biol. 52:1980;257-272.
29. Kuroki M., Kamo N., Kobatake Y., Okimasu E., Utsumi K. Measurement of membrane potential in polymorphonuclear leukocytes and its changes during surface stimulation. Biochim. Biophys. Acta. 693:1982;326-334.
30. Tsunoda Y., Matsumiya H. Calcium-activated membrane depolarisation via modulation of chloride efflux from parietal cells during gastrin stimulation. FEBS Lett. 222:1987;149-153.
31. Martin M. A., Nauseef W. M., Clark R. A. Depolarization blunts the oxidative burst of human neutrophils. Parallel effects of monoclonal antibodies, depolarizing buffers, and glycolytic inhibitors. J. Immunol. 140:1988;3928-3935.
32. - efflux. Am. J. Physiol. 259:1990;C531-C540.
33. Kiefer H., Schulze R. The membrane potential of lymphocytes changes only in response to specific stimulation. Biosci. Rep. 2:1982;583-588.
34. Henry-Toulme N., Sarthou P., Bolard J. Early membrane potential and cytoplasmic calcium changes during mitogenic stimulation of WEHI 231 cell line by polyene antibiotics, lipopolysaccharide and anti-immunoglobulin. Biochim. Biophys. Acta. 1051:1990;285-292.
35. Iwagaki H., Fuchimoto S., Miyake M., Aoki H., Orita K. Interferon-gamma activates the voltage-gated calcium channel in RPMI 4788 cells. Biochem. Biophys. Res. Commun. 153:1988;1276-1281.
36. Novak M. J., Cohen H. J. Depolarization of polymorphonuclear leukocytes by Porphyromonas (Bacteroides) gingivalis 381 in the absence of respiratory burst activation. Infect. Immun. 59:1991;3134-3142.
37. 2+ influx into platelets by platelet-activating factor and other aggregation inducers. Eur. J. Biochem. 198:1991;267-273.
38. Ince C., Coremans J. M. C. C., Ypey D. L., Leijh P. C. J., Verveen A. A., van Furth R. Phagocytosis by human macrophages is accompanied by changes in ionic channel currents. J. Cell Biol. 106:1988;1873-1878.
39. McKinney L. C., Gallin E. K. Effect of adherence, cell morphology, and lipopolysaccharide on potassium conductance and passive membrane properties of murine macrophages J774.1 cells. J. Membrane Biol. 116:1990;47-56.
40. + current in macrophages by platelet activating factor. Biochem. Biophys. Res. Commun. 182:1992;372-378.
41. Pandiella A., Magni M., Lovisolo D., Meldolesi J. The effects of epidermal growth factor on membrane potential. Rapid hyperpolarization followed by persistent fluctuations. J. Biol. Chem. 264:1989;12914-12921.
42. Chen G., Yamamoto Y., Miwa K., Suzuki H. Hyperpolarization of arterial smooth muscle induced by endothelial humoral substances. Am. J. Physiol. 260:1991;H1888-H1892.
43. Klyubin I. V., Kirpichnikova K. M., Gamaley I. A. Hydrogen peroxide-induced chemotaxis of mouse peritoneal neutrophils. Eur. J. Cell Biol. 70:1996;347-351.
44. 2+-activated ion channels in human neutrophils. J. Clin. Invest. 85:1990;491-498.
45. Alonso-Torre S. R., Trautmann A. Calcium responses elicited by nucleotides in macrophages interaction between two receptor subtypes. J. Biol. Chem. 268:1993;18640-18647.
46. Gallin E. K. Calcium and voltage activated potassium channels in human macrophages. Biophys. J. 46:1984;821-827.
47. + conductances. J. Membrane Biol. 103:1988;55-66.
48. Soldati L., Persechini P. M. Depolarization of macrophage polykaryons in the absence of external sodium induces a cyclic stimulation of a calcium-activated potassium conductance. Biochim. Biophys. Acta. 972:1988;283-292.
49. Tare M., Parkington H. C., Coleman H. A., Neild T. O., Dusting G. J. Hyperpolarization and relaxation of arterial smooth muscle caused by nitric oxide derived from endothelium. Nature. 346:1990;69-71.
50. Kuo S. S., Saad A. H., Koong A. C., Hahn G. M., Giaccia A. J. Potassium-channel activation in response to low doses of gamma-irradiation involves reactive oxygen intermediates in nonexcitatory cells. Proc. Natl. Acad. Sci. U. S. A. 90:1993;908-912.
51. Fialkow L., Chan C. K., Grinstein S., Downey G. P. Regulation of tyrosine phosphorylation in neutrophils by the NADPH oxidase. Role of reactive oxygen intermediates. J. Biol. Chem. 268:1993;17131-17137.
52. Nose K., Ohba M. Functional activation of the egr-1 (early growth response-1) gene by hydrogen peroxide. Biochem. J. 316:1996;381-383.