Maitotoxin-induced calcium influx in erythrocyte ghosts and rat glioma C6 cells, and blockade by gangliosides and other membrane lipids

Chemical Research in Toxicology

Volumn 12, Issue 10, 1999, Pages 993-1001

  Konoki, Keiichi ^a   Hashimoto, Masaki ^a   Murata, Michio ^a,b   Tachibana, Kazuo ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ION; CONCANAVALIN A; FLUORESCENT DYE; FURA 2; GANGLIOSIDE; GANGLIOSIDE GM1; GANGLIOSIDE GM3; GLYCOSPHINGOLIPID; LECTIN; MAITOTOXIN; MEMBRANE LIPID; OLIGOSACCHARIDE; SIALIC ACID; TUNICAMYCIN;

ANIMAL CELL; ARTICLE; CALCIUM TRANSPORT; CAPPING PHENOMENON; CELL MEMBRANE; CELL SURFACE; CONTROLLED STUDY; ERYTHROCYTE GHOST; GLIOMA CELL; GLYCOSYLATION; NONHUMAN; RAT;

ANIMALS; ANTI-BACTERIAL AGENTS; BRAIN NEOPLASMS; CALCIUM; CALCIUM RADIOISOTOPES; CONCANAVALIN A; ERYTHROCYTE MEMBRANE; FLUORESCENT DYES; FURA-2; GANGLIOSIDES; GLIOMA; MARINE TOXINS; MEMBRANE LIPIDS; MEMBRANE POTENTIALS; MODELS, MOLECULAR; MOLECULAR CONFORMATION; OXOCINS; RATS; TUMOR CELLS, CULTURED; TUNICAMYCIN;

ANIMALIA;

EID: 0032706518     PISSN: 0893228X     EISSN: None     Source Type: Journal    
DOI: 10.1021/tx990014m     Document Type: Article

References (40)

1. Yasumoto, T., Bagnis, R., and Vernoux, J. P. (1976) Toxicity of surgeonfish 2. Properties of the principal water-soluble toxin. Bull. Jpn. Soc. Fish. 42, 359-365.
2. Yokoyama, A., Murata, M., Oshima, Y., Iwashita, T., and Yasumoto, T. (1988) Some chemical properties of maitotoxin, a putative calcium channel agonist isolated from a marine dinoflagellate. J. Biochem. 104, 184-187.
3. Murata, M., Naoki, H., Matsunaga, S., Satake, M., and Yasumoto, T. (1994) Structure and partial stereochemical assignments for maitotoxin, the most toxic and largest natural non-biopolymer. J. Am. Chem. Soc. 116, 7098-7107.
4. Sasaki, M., Matsumori, N., Maruyama,T., Nonomura, T., Murata, M., Tachibana, K., and Yasumoto, T. (1996) The complete structure of maitotoxin, part I: Configuration of the C1-C14 side chain. Angew. Chem., Int. Ed. 35, 1672-1675.
5. Zheng, W., DeMattei, J. A., Wu, J.-P., Duan, J. J.-W., Cook, L. R., Oinuma, H., and Kishi, Y. (1996) Complete relative stereochemistry of maitotoxin. J. Am. Chem. Soc. 118, 7946-7968.
6. Gusovsky, F., and Daly, J. W. (1990) Maitotoxin: a unique pharmacological tool for research on calcium-dependent mechanisms. Biochem. Pharmacol. 39, 1633-1639.
7. Gusovsky, F., Yasumoto, T., and Daly, J. W. (1989) Maitotoxin, a potent, general activator of phosphoinositide breakdown. FEBS Lett. 243, 307-312.
8. Choi, O. H., Padgett, W. L., Nishizawa, Y., Gusovsky, F., Yasumoto, T., and Daly, J. W. (1989) Maitotoxin: effects on calcium channels, phosphoinositide breakdown, and arachinodate release in pheochromocytoma PC12 cells. Mol. Pharmacol. 37, 222-230.
9. Ohizumi, Y., Kajiwara, A., and Yasumoto, T. (1983) Excitatory effect of the most potent marine toxin, maitotoxin, on the Guinea-pig vas deferens. J. Pharmacol. Exp. Ther. 227, 199-204.
10. Taglialatela, M., Amoroso, S., Yasumoto, T., Renzo, G. D., and Annunziato, L. (1986) Maitotoxin and BAY-K-8644: two putative calcium channel activators with different efects on endogeneous dopamine release from tuberoinfundibular neurons. Brain Res. 381, 356-358.
11. 2+ channel activating function of maitotoxin, the most potent marine toxin known, in clonal rat pheochromocytoma cells. J. Biol. Chem. 258, 10944-10949.
12. Soergel, D., Gusovsky, F., Yasumoto, T., and Daly, J. W. (1990) Stimulatory effects of maitotoxin on insulin release in insulinoma HIT cells: role of calcium uptake and phosphoinositide breakdown. J. Pharmacol. Exp. Ther. 255, 1360-1365.
13. 1 pituitary cells via activation of type L voltage-dependent calcium channels. J. Biol. Chem. 267, 25025-25031.
14. 1 rat pituitary cells nimodipine-sensitive and -insensitive mechanisms. Biochem. Pharmacol. 51, 759-769.
15. Soergel, D., Yasumoto, T., Daly, J. W., and Gusovsky, F. (1992) Maitotoxin effects are blocked by SK&F 96365, an inhibitor of receptor-mediated calcium entry. Mol. Pharmacol. 41, 487-493.
16. 2+ flux in cells by maitotoxin. Eur. J. Pharmacol. 227, 43-49.
17. Nishio, M., Muramatsu, I., and Yasumoto, T. (1996) Na-permeable channels induced by maitotoxin in Guinea-pig single ventricular cells. Eur. J. Pharmacol. 297, 293-298.
18. Escobar, L. I., Salvador, C., Martinez, M., and Vaca, L. (1998) Maitotoxin, a cationic channel activator. Neurobiology 6, 59-74.
19. Daly, J. W., Lueder, J., Padgett, W. L., Yangmee, S., and Gusovsky, F. (1995) Maitotoxin-elicited calcium influx in cultured cells: effect of calcium-channel blockers. Biochem. Parmacol. 50, 1187-1197.
20. 2+ influx in rat glioma C6 cells by alkylamines. J. Nat. Toxins 5, 209-217.
21. Bressler, J. P., Belloni-Olivi, L., and Forman, S. (1993) Effect of ganglioside GM1 on arachidonic acid release in bovine aortic endothelial cells. Life Sci. 54, 49-60.
22. Trainer, V. L., Baden, D. G., and Catterall, W. A. (1994) Identification of peptide components of the brevetoxin receptor site of rat brain sodium channels. J. Biol. Chem. 269, 19904-19909.
23. Gawley, R. E., Rein, K. S., Jeglitsch, G., Adams, D. J., Theodorakis, E. A., Tiebes, J., Nicolaou, K. C., and Baden, D. G. (1995) The relationship of brevetoxin "length" and A-ring functionality to binding and activity in neuronal sodium channels. Chem. Biol. 2, 533-541.
24. Matile, S., Berova, N., and Nakanishi, K. (1996) Exciton coupled circular dichroic studies of self-assembled brevetoxin-porphyrin conjugates in lipid bilayers and polar solvents. Chem. Biol. 3, 379-392.
25. Matile, S., and Nakanishi, K. (1996) Selective cation movement across lipid bilayers containing brevetoxin B. Angew. Chem., Int. Ed. 35, 757-759.
26. 2+ pump revealed by fluorescent chelator dyes in human red blood cell ghosts. J. Gen. Physiol. 99, 41-62.
27. 2+ indicators with greatly improved fluorescence properties. J. Biol. Chem. 260, 3440-3450.
28. i oscillations in transgenically derived β-cells. J. Biol. Chem. 263, 10402-10410.
29. Loew, L. M., Benson, L., Lazarovici, P., and Rosenberg, I. (1985) Fluorometric analysis of transferable membrane pores. Biochemistry 24, 2101-2104.
30. Sladeczek, F., Schmidt, B. H., Alonso, R., Vian, L., Tep, A., Yasumoto, T., Cory, R. N., and Bockaert, J. (1988) New insights into maitotoxin action. Eur. J. Biochem. 174, 663-670.
31. Thomas, A. P., and Delaville, F. (1991) The use of fluorescent indicators for measurements of cytosolic-free calcium concentration in cell populations and single cells. In Cellular Calcium (McCormack J. G., and Cobbold, P. H., Eds.) pp 1-53, IRL Press, Oxford, U.K.
32. Leavitt, R., Schlesinger, S., and Kornfeld, S. (1977) Tunicamycin inhibits glycosylation and multiplication of sindbis and vesicular stomatitis viruses. J. Virol. 21, 375-385.
33. Burger, M. M., and Noonan, K. D. (1970) Restoration of normal growth by covering of agglutinin sites on tumor cell surface. Nature 228, 512-515.
34. 2+ channel activator candidate. J. Biol. Chem. 257, 7287-7289.
35. 2+ entry into synaptosomes. Eur. J. Pharmacol. 122, 379-380.
36. 2+ levels and membrane potential in purified rat brain synaptosomes. Biochim. Biophys. Acta 1026, 126-132.
37. 2+ entry in MDCK renal epithelial cells. Mol. Pharmacol. 45, 300-305.
38. Thompson, T. E., and Tillack, T. W. (1985) Organization of glycosphingolipids in bilayers and plasma membranes of mamalian cells. Annu. Rev. Biophys. Biophys. Chem. 14, 361-386.
39. Miller-Podraza, H., Bradley, R. M., and Fishman, P. H. (1982) Biosynthesis and localization of gangliosides in cultured cells. Biochemistry 21, 3260-3265.
40. Acquotti, D., Fronza, G., Ragg, E., and Sonnino, S. (1991) Three-dimensional structure of GD1b and GD1b-monolactone gangliosides in dimethylsulphoxide: a nuclear Overhauser effect investigation supported by molecular dynamics calculations. Chem. Phys. Lipids 59, 107-125.