ATP-dependent copper transporter, in the Golgi apparatus of rat hepatocytes, transports Cu(II) not Cu(I)

American Journal of Physiology - Gastrointestinal and Liver Physiology

Volumn 271, Issue 5 34-5, 1996, Pages

  Bingham, M J ^b   Ong, T J ^b   Ingledew, W J ^b   McArdle, H J ^a  

^a UNIVERSITY OF DUNDEE   (United Kingdom)

^b NONE

Author keywords

adenosine 5' triphosphate dependent transport; ATP7B; Wilson disease

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATE; ALKALINE PHOSPHATASE; CARRIER PROTEIN; COPPER ION; DIVALENT CATION; GALACTOSYLTRANSFERASE; MONOVALENT CATION;

ANIMAL TISSUE; ARTICLE; GOLGI COMPLEX; ION TRANSPORT; LIVER MICROSOME; NONHUMAN; PRIORITY JOURNAL; RAT; WILSON DISEASE;

EID: 0029847157     PISSN: 01931857     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpgi.1996.271.5.g741     Document Type: Article

References (29)

1. Askwith, C., D. Eide, A. van Ho, P. Bernard S, L. Li, S. Davis-Kaplan, D. Sipe, and J. Kaplan. The FET3 gene of S. cerevisiae encodes a multicopper oxidase required for ferrous iron uptake. Cell 76: 403-410, 1994.
2. Bingham, M. J., A. Burchell, and H. J. McArdle. Identification of an ATP-dependent copper transport system in endoplasmic reticulum vesicles isolated from rat liver. J. Physiol. Lond. 482: 583-587, 1995.
3. Bradford, M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal. Biochem. 72: 248-254, 1976.
4. Bremner, I. Involvement of metallothionein in the hepatic metabolism of copper. J. Nutr. 117: 19-29, 1987.
5. Bull, P. C., G. R. Thomas, J. M. Rommens, J. R. Forbes, and D. W. Cox. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nature Genet. 5: 327-337, 1993.
6. Dijkstra, M., G. In't Veld, G. J. van den Berg, M. Muller, F. Kuipers, and R. J. Vonk. Adenosine triphosphate-dependent copper transport in isolated rat liver plasma membrane. J. Clin. Invest. 95: 412-416, 1995.
7. Dijkstra, M., F. Kuipers, R. Havinga, E. P. Smit, and R. J. Vonk. Bile secretion of trace elements in rats with a congenital defect in hepatobiliary transport of glutathione. Pediatr. Res. 28: 339-343, 1990.
8. Durnam, D. M., F. Perrin, F. Gannon, and R. D. Palmiter. Isolation and characterization of the mouse metallothionein-I gene. Proc. Natl. Acad. Sci. USA 77: 6511-6515, 1980.
9. Farrell, R. A., H. J. McArdle, and J. Camakaris. Effects of metallothionein on the observed copper distribution in cell extracts. J. Inorg. Biochem. 48: 303-316, 1993.
10. Freedman, J. H., M. R. Ciriolo, and J. Peisach. The role of glutathione in copper metabolism and toxicity. J. Biol. Chem. 264: 5598-5605, 1989.
11. Freedman, J. H., and J. Peisach. Intracellular copper transport in cultured hepatoma cells. Biochem. Biophys. Res. Commun. 164: 134-140, 1989.
12. Freedman, J. H., R. J. Weiner, and J. Peisach. Resistance to copper toxicity of cultured hepatoma cells. J. Biol. Chem. 261: 11840-11848, 1986.
13. Houwen, R., M. Dijkstra, F. Kuipers, E. P. Smit, R. Havinga, and R. J. Vonk. Two pathways for biliary copper excretion in the rat. The role of glutathione. Biochem. Pharmacol. 39: 1039-1044, 1990.
14. Keusch, J., P. M. Lydyard, D. A. Isenberg, and P. J. Delves. β-1,4-Galactosyltransferase activity in B cells detected using a simple ELISA-based assay. Glycobiology 5: 365-370, 1995.
15. Linder, M. C. Biochemistry of copper. In: Biochemistry of the Elements, edited by E. Frieden. New York: Plenum, 1991, p. 331-342.
16. McArdle, H. J. The transport of iron and copper across the cell membrane: different mechanisms for different metals? Proc. Nutr. Soc. 51: 199-209, 1992.
17. McArdle, H. J., S. M. Gross, I. Creaser, A. M. Sargeson, and D. M. Danks. The effect of chelators on copper metabolism and copper pools in mouse hepatocytes. Am. J. Physiol. 256 (Gastrointest. Liver Physiol. 19): G667-G672, 1989.
18. Palida, F. A., and M. J. Ettinger. Identification of proteins involved in intracellular copper metabolism. J. Biol. Chem. 266: 4586-4592, 1991.
19. Palida, F. A., A. Mas, K. Bethin, P. A. Lonergan, and M. J. Ettinger. Cytosolic copper-binding proteins in rat and mouse hepatocytes incubated continuously with Cu(II). Biochem. J. 268: 359-366, 1990.
20. Petrukhin, K., S. G. Fischer, M. Pirastu, R. E. Tanzi, I. Chernov, M. Devoto, L. M. Brzustowicz, E. Cayanis, E. Vitale, J. J. Russo, D. Matseoane, B. Boukhgalter, W. Wasco, A. L. Figus, J. Loudianos, A. Cao, I. Sternlieb, O. Egrafov, E. Parano, L. Pavone, D. Warburton, J. Ott, G. K. Penchaszadeh, I. H. Scheinberg, and T. C. Gilliam. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene. Nature Genet. 5: 338-343, 1993.
21. Rickwood, D. (Editor). Preparative Centrifugation. A Practical Approach. Oxford, UK: Oxford University Press, 1992.
22. Seagrave, J., J. L. Hanners, W. Taylor, and H. A. O'Brien. Transfer of copper from metallothionein to nonmetallothionein proteins in cultured cells. Biol. Tracer Elem. Res. 10: 163-173, 1986.
23. Solioz, M., and A. Odermatt. Copper and silver transport by CopB-ATPase in membrane vesicles of Enterococcus hirae. J. Biol. Chem. 270: 9217-9221, 1995.
24. Solioz, M., A. Odermatt, and R. Krapf. Copper pumping ATPases: common concepts in bacteria and man. FEBS Lett. 346: 44-47, 1994.
25. Tanzi, R. E., K. Petrukhin, I. Chernov, J. L. Pellequer, W. Wasco, B. Ross, D. M. Romano, E. Parano, L. Pavone, L. M. Brzustowicz, M. Devoto, J. Peppercorn, A. I. Bush, I. Sternlieb, M. Pirastu, J. F. Gusella, O. Evgrafov, G. K. Penchaszadeh, B. Honig, I. S. Edelman, M. B. Soares, I. H. Scheinberg, and T. C. Gilliam. The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Nature Genet. 5: 344-350, 1993.
26. Terada, K., Y. Kawarada, N. Miura, O. Yasui, K. Koyama, and T. Sugiyama. Copper incorporation into ceruloplasmin in rat livers. Biochim. Biophys. Acta 1270: 58-62, 1995.
27. 67Cu. Am. J. Physiol. 224: 682-686, 1973.
28. Van den Berg, G. J., and H. J. McArdle. A plasma membrane NADH oxidase is involved in copper uptake by plasma membrane vesicles isolated from rat liver. Biochim. Biophys. Acta 1195: 276-280, 1994.
29. Yuan, D. S., R. Stearmen, A. Dancis, T. Dunn, T. Beeler, and R. D. Klausner. The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake. Proc. Natl. Acad. Sci. USA 92: 2632-2636, 1995.