Plasma membrane depolarization reduces nitric oxide (NO) production in P388D.1 macrophage-like cells during Leishmania major infection

Cellular Immunology

Volumn 222, Issue 1, 2003, Pages 58-68

  Scott, Kristine D ^a   Stafford, James L ^a   Galvez, Fernando ^a   Belosevic, Miodrag ^a   Goss, Greg G ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

Author keywords

K+ channels; Membrane potential; Nitric oxide; Protozoan parasites; Vm

Indexed keywords

2 AMINO 4 PHOSPHONOBUTYRIC ACID; NITRIC OXIDE; POTASSIUM CHANNEL; POTASSIUM CHANNEL BLOCKING AGENT; QUININE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CELL MEMBRANE DEPOLARIZATION; CELL STRAIN; CONTROLLED STUDY; DRUG EFFECT; HOST CELL; LEISHMANIA MAJOR; MACROPHAGE; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROMASTIGOTE; PROTOZOAL INFECTION;

CINCHONA PUBESCENS; LEISHMANIA MAJOR; PROTOZOA;

EID: 0037869114     PISSN: 00088749     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0008-8749(03)00077-7     Document Type: Article

References (44)

1. Brown H., Kozlowski R., Perry H. The importance of ion channels for macrophage and microglial activation in vitro. Glia. 22:1998;94-97.
2. Stuehr D.J., Marletta M.A. Induction of nitrite, nitrate synthesis in murine macrophages by BCG infection, lymphokines, or interferon-γ J. Immunol. 139:1987;518-525.
3. Marletta M.A., Yoon P.S., Iyengar R., Leaf C.D., Wishnok J.S. Macrophage oxidation of L-arginine to nitrite and nitrate - nitric-oxide is an intermediate. Biochemistry. 27:1988;8706-8711.
4. Palmer R.M.J., Ferrige A.G., Moncada S. Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor. Nature. 327:1987;524-526.
5. James S.L. Role of nitric oxide in parasitic infections. Microbiol. Rev. 59:1995;533-547.
6. Alexander J., Russell D.J. The interaction of Leishmania species with macrophages. Adv. Parasitol. 31:1992;175-254.
7. Kane M.M., Mosser D.M. Leishmania parasites and their ploys to disrupt macrophage activation. Curr. Opin. Hematol. 7:2000;26-31.
8. Nandan D., Lo R., Reiner N.E. Activation of phosphotyrosine phosphatase activity attenuates mitogen-activated protein kinase signaling and inhibits c-FOS and nitric oxide synthase expression in macrophages infected with Leishmania donovani. Infect. Immun. 67(8):1999;4055-4063.
9. Olivier M., Romero-Gallo B.-J., Matte C., Blanchette J., Posner B.I., Tremblay M.J., Faure R. Modulation of interferon-γ-induced macrophage activation by phosphotyrosine phosphatase inhibition. Effect on murine Leishmaniasis progression. J. Biol. Chem. 273(22):1998;13944-13949.
10. Descoteaux A., Turco S.J., Sacks D.L., Matlashewski G. Leishmania donovani lipophosphoglycan selectively inhibits signal transduction in macrophages. J. Immunol. 146(8):1991;2747-2753.
11. Assreuy J., Cunha F.Q., Epperlein M., Noronha-Dutra A., O'Donnell C.A., Liew F.Y., Moncada S. Production of nitric oxide and superoxide by activated macrophages and killing of Leishmania major. Eur. J. Immunol. 24:1994;672-676.
12. Green S.J., Meltzer M.S., Hibbs J.B. Jr., Nacy C.A. Activated macrophages destroy intracellular Leishmania major amastigotes by an L-arginine-dependent killing mechanism. J. Immunol. 144(1):1990;278-283.
13. Liew F.Y., Li Y., Millott S. Tumor necrosis factor-α synergizes with IFN-γ in mediating killing of Leishmania major through the induction of nitric oxide. J. Immunol. 145(12):1990;4306-4310.
14. Liew F.Y., Li Y., Moss D., Parkinson C., Rogers M.V., Moncada S. Resistance to Leishmania major infection correlates with the induction of nitric oxide synthase in murine macrophages. Eur. J. Immunol. 21:1991;3009-3014.
15. Descoteaux A., Prive C. Leishmania donovani promastigotes evade the activation of mitogen-activated protein kinases p38, c-Jun N-terminal kinase, and extracellular signal-related kinase-1/2 during infection in naïve macrophages. Eur. J. Immunol. 30:2000;2235-2244.
16. Nandan D., Knutson K.L., Lo R., Reiner N.E. Exploitation of host cell signaling machinery: activation of macrophage phosphotyrosine phosphatases as a novel mechanism of molecular microbial pathogenesis. J. Leuk. Biol. 67:2000;464-470.
17. Ray M., Gam A.A., Boykins R.A., Kenney R.T. Inhibition of interferon-γ signaling by Leishmania donovani. J. Infect. Dis. 181:2000;1121-1128.
18. Feng G.-.J., Goodridge H.S., Harnett M.M., Wei X.-.Q., Nikolaev A.V., Higson A.P., Liew F.Y. Extracellular signal-related kinase (ERK) and p38 mitogen-activated protein (MAP) kinases differentially regulate the lipopolysaccharide-mediated induction of inducible nitric oxide synthase and IL-12 in macrophages: Leishmania phosphoglycans subvert macrophage Il-12 production by targeting ERK MAP kinase. J. Immunol. 163:1999;6403-6412.
19. Calahan M.D., Wulff H., Chandy K.G. Molecular properties and physiological roles of ion channels in the immune system. J. Clin. Immunol. 21(4):2001;235-252.
20. 2+ -mediated monocyte function Am. J. Physiol. Cell Physiol. 283:2002;C990-C1000.
21. + channels improves experimental autoimmune encephalomyelitis and inhibits T cell activation J. Immunol. 166:2001;936-944.
22. + channel. J. Immunol. 159:1997;6209-6215.
23. Gallin E.K. Ion channels in leukocytes. Physiol. Rev. 71:1991;775-811.
24. Gallin E.K., Livengood D.R. Inward rectification in mouse macrophages: evidence for a negative resistance region. Am. J. Physiol. Cell Physiol. 241(1):1981;C9-C17.
25. + conductances J. Membr. Biol. 103:1988;55-66.
26. Hille B. Ionic Channels of Excitable Membranes. 2nd ed. 1992;Sinauer Associates, Sunderland.
27. Randriamampita C., Trautmann A. Ionic channels in murine macrophages. J. Cell Biol. 105:1987;761-769.
28. Lowry M.A.R., Goldberg J.I., Belosevic M. Induction of nitric oxide (NO) synthesis in murine macrophages requires potassium channel activity. Clin. Exp. Immunol. 111:1998;597-603.
29. Forero M.E., Marin M., Corrales A., Llano I., Moreno H., Comacho M. Leishmania amazonensis infection induces changes in the electrophysiological properties of macrophage-like cells. J. Membr. Biol. 170:1999;173-180.
30. + channel blocking by aminopyridines Biophys. Chem. 96(1):2002;1-14.
31. Koren H.S., Handwergen B.S., Wunderlich J.R. Identification of macrophage-like characteristics in a cultured murine tumor line. J. Immunol. 114:1975;894-897.
32. Belosevic M., Davis C.E., Meltzer M.S., Nacy C.A. Regulation of activated macrophage antimicrobial activities. Identification of lymphokines that cooperate with IFN-γ for induction of resistance to infection. J. Immunol. 141(3):1988;890-896.
33. Green L.C., Wagner D.A., Glogowski J., Skipper P.L., Wishnok J.S., Tannenbaum S.R. Analysis of nitrate, nitrite, and 15-nitrate in biological fluids. Anal. Biochem. 126:1982;131-138.
34. Dall'Asta V., Gatti R., Orlandini G., Rossi P., Rotoli B., Sala R., Bussolati O., Gazzola G. Membrane potential changes visualizes in complete growth media through confocal laser scanning microscopy of bis-oxonol-loaded cells. Exp. Cell Res. 231:1997;260-268.
35. Grissmer S., Nguyen A.N., Cahalan M.D. Calcium-activated potassium channels in resting and activated human T lymphocytes. Expression levels, calcium dependence, ion selectivity, and pharmacology. J. Gen. Physiol. 102(4):1993;601-630.
36. Gallin E.K., Sheehy P.A. Differential expression of inward and outward potassium currents in the macrophage-like cell line J774.1. J. Physiol. 369:1985;475-500.
37. Chandy K.G., Gutman G.A., Grissmer S. Physiological role, molecular structure, and evolutionary relationships of voltage gated potassium channels in T lymphocytes. Sem. Neurosci. 5:1993;125-134.
38. Thompson S. Aminopyridine block of transient potassium current. J. Gen. Physiol. 80:1980;1-18.
39. Eder C. Ion channels in microglia (brain macrophages). Am. J. Physiol. Cell Physiol. 275(44):1998;C327-C342.
40. Maruyama N., Kakuta Y., Yamauchi K., Ohkawara Y., Aizawa T., Ohrui T., Nara M., Oshiro T., Ohno I., Tamura G. Quinine inhibits production of tumor necrosis factor-α from human alveolar macrophages. Am. J. Respir. Cell Mol. Biol. 10(5):1994;514-520.
41. Haslberger A., Romanin C., Koerber R. Membrane potential modulates release of tumor necrosis factor in lipopolysaccharide-stimulated mouse macrophages. Mol. Biol. Cell. 3:1992;451-460.
42. Schlicter L., Sidell N., Hagiwara S. Potassium channels mediate killing in human natural killer cells. Proc. Natl. Acad. Sci. USA. 83:1986;451-455.
43. + flux Nature. 416:2002;291-297.
44. + channel in transmembrane signaling J. Immunol. 166:2001;1009-1015.