Silver activates mast cells through reactive oxygen species production and a thiol-sensitive store-independent Ca2+ influx

Free Radical Biology and Medicine

Volumn 40, Issue 11, 2006, Pages 1949-1959

  Yoshimaru, Tetsuro ^a   Suzuki, Yoshihiro ^a   Inoue, Toshio ^a   Niide, Osamu ^a   Ra, Chisei ^a  

^a NIHON UNIVERSITY   (Japan)

Author keywords

Ca2+ influx; Free radicals; Mast cells; Reactive oxygen species; Silver

Indexed keywords

CALCIUM; DITHIOTHREITOL; EBSELEN; FLUORESCENT DYE; FREE RADICAL; MANGANESE TETRAKIS 4 (BENZOIC ACID)PORPHYRIN; PORPHYRIN DERIVATIVE; REACTIVE OXYGEN METABOLITE; SCOPOLETIN; SILVER; SILVER DERIVATIVE; SILVER SULFATE; THIOL; UNCLASSIFIED DRUG; WORTMANNIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CALCIUM TRANSPORT; CELL ACTIVATION; CELL CULTURE; CONTROLLED STUDY; DEGRANULATION; DRUG ACTIVITY; DRUG INHIBITION; DRUG RESPONSE; FLOW CYTOMETRY; LEUKEMIA CELL; MAST CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL;

1-PHOSPHATIDYLINOSITOL 3-KINASE; ANIMALS; CALCIUM; CELL DEGRANULATION; ENZYME ACTIVATION; FLOW CYTOMETRY; ION TRANSPORT; LUMINESCENCE; MAST CELLS; MICE; MICE, INBRED C57BL; OXIDATION-REDUCTION; REACTIVE OXYGEN SPECIES; SILVER; SULFHYDRYL COMPOUNDS;

ANIMALIA;

EID: 33646561541     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2006.01.023     Document Type: Article

References (38)

1. Eneström S., and Hultman P. Does amalgam affect the immune system? A controversial issue. Int. Arch. Allergy Immunol. 106 (1995) 180-203
2. Anderson T., and Bruze M. In vivo testing of the protective efficacy of gloves against allergen-containing products using an open chamber system. Contact Dermatitis 41 (1999) 260-263
3. Budinger L., and Hertl M. Immunologic mechanisms in hypersensitivity reactions to metal ions: an overview. Allergy 55 (2000) 108-115
4. Martin S.F. T lymphocyte-mediated immune responses to chemical haptens and metal ions: implications for allergic and autoimmune disease. Int. Arch. Allergy Immunol. 134 (2004) 186-198
5. Thierse H.J., Gamerdinger K., Junkes C., Guerreiro N., and Weltzien H.U. T cell receptor (TCR) interaction with haptens: metal ions as non-classical haptens. Toxicology 209 (2005) 101-107
6. Röger J., Zillikens D., Hartmann A.A., Burg G., and Gleichmann E. Systemic autoimmune disease in a patient with long-standing exposure to mercury. Eur. J. Dermatol. 2 (1992) 168-170
7. Fournie G.J., Saoudi A., Druet P., and Pelletier L. Th2-type immunopathological manifestations induced by mercury chloride or gold salts in the rat: signal transduction pathways, cellular mechanisms and genetic control. Autoimmun. Rev. 1 (2002) 205-212
8. Galli S.J., Kalesnikoff J., Grimbaldeston M.A., Piliponsky A.M., Williams C.M., and Tsai M. Mast cells as "tunable" effector and immunoregulatory cells: recent advances. Annu. Rev. Immunol. 23 (2005) 749-786
9. Kiely P.D.W., Pecht I., and Oliveira D.B.G. Mercuric chloride-induced vasculitis in the Brown Norway rat: αβ T-cell dependent and -independent phase: role of the mast cell. J. Immunol. 159 (1997) 5100-5106
10. Rottem M., and Mekori Y.A. Mast cells and autoimmunity. Autoimmun. Rev. 4 (2005) 21-27
11. Marshall J.S., and Jawdat D.M. Mast cells in innate immunity. J. Allergy Clin. Immunol. 114 (2004) 21-27
12. Galli S.J., Nakae S., and Tsai M. Mast cells in the development of adaptive immune responses. Nat. Immunol. 6 (2005) 135-142
13. Mathieson P.W., Thiru S., and Oliveira D.B. Mercuric chloride-treated brown Norway rats develop widespread tissue injury including necrotizing vasculitis. Lab. Invest. 67 (1992) 121-129
14. Kiely P.D., Thiru S., and Oliveira D.B. Inflammatory polyarthritis induced by mercuric chloride in the Brown Norway rat. Lab. Invest. 73 (1995) 284-293
15. + induces cell degranulation and mediator release. Biochem. Biophys. Res. Commun. 283 (2001) 707-714
16. Suzuki Y., Yoshimaru T., Matsui T., and Ra C. Silver activates calcium signals in rat basophilic leukemia-2H3 mast cells by a mechanism that differs from the FcεRI-activated response. J. Immunol. 169 (2002) 3954-3962
17. Suzuki Y., Yoshimaru T., Inoue T., Niide O., and Ra C. Role of oxidants in mast cell activation. Chem. Immunol. Allergy 87 (2005) 34-42
18. Heneberg P., and Draber P. Regulation of Cys-based protein tyrosine phosphatases via reactive oxygen and nitrogen species in mast cells and basophils. Curr. Med. Chem. 12 (2005) 1859-1871
19. Wu Z., Turner Z.R., and Oliveira D.B. IL-4 gene expression up-regulated by mercury in rat mast cells: a role of oxidant stress in IL-4 transcription. Int. Immunol. 13 (2001) 297-304
20. Wolfreys K., and Oliveira D.B. Alterations in intracellular reactive oxygen species generation and redox potential modulate mast cell function. Eur. J. Immunol. 27 (1997) 297-306
21. Frossi B., De Carli M., Daniel K.C., Rivera J., and Pucillo C. Oxidative stress stimulates IL-4 and IL-6 production in mast cells by an APE/Ref-1-dependent pathway. Eur. J. Immunol. 33 (2003) 2168-2177
22. Suzuki Y., Yoshimaru T., Matsui T., Inoue T., Niide O., Nunomura S., and Ra C. FcεRI signaling of mast cells activates intracellular production of hydrogen peroxide: role in the regulation of calcium signals. J. Immunol. 171 (2003) 6119-6127
23. Yoshimaru T., Suzuki Y., Matsui T., Yamashita K., Ochiai T., Yamaki M., and Shimizu K. Blockade of superoxide generation prevents high-affinity immunoglobulin E receptor-mediated release of allergic mediators by rat mast cell line and human basophils. Clin. Exp. Allergy 32 (2002) 612-618
24. 2 release by human blood monocytes and mouse peritoneal macrophages. J. Immunol. Methods 78 (1985) 323-336
25. 2 production, in vitro, from Kupffer cells stimulated by phorbol myristate acetate. FEBS Lett. 335 (1993) 167-170
26. Swindle E.J., Metcalfe D.D., and Coleman J.W. Rodent and human mast cells produce functionally significant intracellular reactive oxygen species but not nitric oxide. J. Biol. Chem. 279 (2004) 48751-48759
27. Schewe T. Molecular actions of ebselen-an antiinflammatory antioxidant. Gen. Pharmacol. 26 (1995) 1153-1169
28. Putney Jr. J.W., Broad L.M., Braun F.J., Lievremont J.P., and Bird G.S. Mechanisms of capacitative calcium entry. J. Cell Sci. 114 (2001) 2223-2229
29. 2+ entry: dynamic interplay between endoplasmic reticulum, mitochondria and plasma membrane. J. Physiol. 547 (2003) 333-348
30. Saitoh S., Arudchandran R., Manetz T.S., Zhang W., Sommers C.L., Love P.E., Rivera J., and Samelson L.E. LAT is essential for FcεRI-mediated mast cell activation. Immunity 12 (2000) 525-535
31. Rivera J. Molecular adapters in FcεRI signaling and the allergic response. Curr. Opin. Immunol. 14 (2002) 688-693
32. Karlsson A., Nixon J.B., and McPhail L.C. Phorbol myristate acetate induces neutrophil NADPH-oxidase activity by two separate signal transduction pathways: dependent or independent of phosphatidylinositol 3-kinase. J. Leukocyte Biol. 67 (2000) 396-404
33. Robinson C.J., Abraham A.A., and Balazs T. Induction of anti-nuclear antibodies by mercuric chloride in mice. Clin. Exp. Immunol. 28 (1984) 300-306
34. Hultman P., Enestrom S., Turley S.J., and Pollard K.M. Selective induction of anti-fibrillarin autoantibodies by silver nitrate in mice. Clin. Exp. Immunol. 96 (1994) 285-291
35. Prouvost-Danon A., Abadie A., Sapin C., Bazin H., and Druet P. Induction of IgE synthesis and potentiation of anti-ovalbumin IgE antibody response by HgCl2 in the rat. J. Immunol. 126 (1981) 699-792
36. Pusey C.D., Bowman C., Morgan A., Weetman A.P., Hartley B., and Lockwood C.M. Kinetics and pathogenicity of autoantibodies induced by mercuric chloride in the brown Norway rat. Clin. Exp. Immunol. 81 (1990) 76-82
37. Esnault V.L., Mathieson P.W., Thiru S., Oliveira D.B., and Martin-Lockwood C. Autoantibodies to myeloperoxidase in brown Norway rats treated with mercuric chloride. Lab. Invest. 67 (1992) 114-120
38. Kiely P.D., Thiru S., and Oliveira D.B. Inflammatory polyarthritis induced by mercuric chloride in the Brown Norway rat. Lab. Invest. 73 (1995) 284-293