Cu metabolism in the liver

Advances in Experimental Medicine and Biology

Volumn 448, Issue , 1999, Pages 29-37

  McArdle, Harry J ^a   Bingham, Michelle J ^b   Summer, Karl ^c   Ong, T J ^b  

^a ROWETT RESEARCH INSTITUTE   (United Kingdom)

^b UNIVERSITY OF DUNDEE   (United Kingdom)

^c INSTITUTE OF EPIDEMIOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSYLHOMOCYSTEINASE; CARRIER PROTEIN; COPPER; GLUTATHIONE; HISTIDINE; OXIDOREDUCTASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; UNCLASSIFIED DRUG; WILSON DISEASE PROTEIN;

CELL MEMBRANE TRANSPORT; CELL METABOLISM; CONFERENCE PAPER; COPPER METABOLISM; ENZYME LOCALIZATION; GENE MUTATION; LIVER; LIVER CELL MEMBRANE; NONHUMAN; PRIORITY JOURNAL; PROTEIN TRANSPORT; REDUCTION; WILSON DISEASE;

EID: 0033278296     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4615-4859-1_3     Document Type: Conference Paper

References (42)

1. Bethin, K.E., Cimato, T.R. and Ettinger, M.J. (1995a). Copper binding to mouse liver S-Adenosylhomocysteine hydrolase and the effects of copper on its levels. J. Biol. Chem. 270, 20703-20711.
2. Bethin, K.E., Petrovic, N. and Ettinger, M.J. (1995b). Identification of a major hepatic copper binding protein as S-adenosylhomocysteine hydrolase. J. Biol. Chem. 270, 20698-20702.
3. Bingham, M.J., Burchell, A. and McArdle, H.J. (1995a). Identification of an ATP dependent copper transport system in endoplasmic reticulum vesicles isolated from rat liver. J. Physiol. 482, 583-587.
4. Bingham, M.J., Ong, T.J., Ingledew, W.J. and McArdle, H.J. (1996). ATP-dependent copper transporter, in the Golgi apparatus of rat hepatocytes, transports Cu(II), not Cu(I). Am. J. Physiol. 271, G741-G746.
5. Bingham, M.J., Ong, T.J., Summer, K.H., Middleton, R.B. and McArdle, H.J. (1998). The physiological function of the Wilson disease gene product, ATP7B. Am. J. Clin. Invest. in press.
6. Bingham, M.J., Sargeson, A.M. and McArdle, H.J. (1997). Identification and characterisation of intracellular copper pools in rat hepatocytes. Am J Physiol. 272, G1400-G1407.
7. Bingham, M.J., van den Berg, G.J. and McArdle, H.J. (1995b). Effect of nutritional copper deficiency on copper uptake by plasma membrane vesicles isolated from rat livers. J. Physiol. 489, 125P.
8. Bull, P.C., Thomas, G.R., Rommens, J.M., Forbes, J.R. and Cox, D.W. (1993). The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nature Genetics. 5, 327-337.
9. Crane, F., Sun, I., Clark, M., Grebing, C. and Low, H. (1985). Transplasma-membrane redox systems in growth and development. Biochim. Biophys. Acta. 811, 233-264.
10. Dancis, A., Klausner, R.D., Hinnebusch, A.G. and Barriocanal, J.G. (1990). Genetic evidence that ferric reductase is required for iron uptake in Saccharomyces cerevisiae. Mol Cell Biol. 10: 2294-2301.
11. Dijkstra, M., In 't Veld, G., van den Berg, G.J., Muller, M., Kuipers, F. and Vonk, R.J. (1995). Adenosine triphosphate-dependent copper transport in isolated rat liver plasma membrane. J. Clin. Invest. 95, 412-416.
12. Ettinger, M.J., Darwish, H.M. and Schmitt, R.C. (1986). Mechanism of copper transport from plasma to hepatocytes. Fed. Proc. 45, 2800-4.
13. Freedman, J.H., Ciriolo, M.R. and Peisach, J. (1989). The role of glutathione in copper metabolism and toxicity. J Biol Chem. 264: 5598-5605.
14. Georgatsou, E., and Alexandraki, D. (1994). 2 distinctly regulated genes are required for ferric reduction, the first step of iron uptake in Saccharomyces cerevisiae. Mol Cell Biol. 14: 3065-3073.
15. Groom, Q.J., Torres, M.A., Fordham-Skelton, A.P., Hammond-Kosack, K.E., Robinson, N.J. and Jones J.D.G. (1996). rbohA, a rice homologue of the mammalian gp91phox respiratory burst oxidase gene. Plant J. 10: 515-522.
16. Klomp, L.W.J., Lin, S., Yuan, D.S., Klausner, R.D., Culotta, V.C. and Gitlin, J.D. (1997). Identification and functional expression of HAHI, a novel human gene involved in copper homeostasis. J Biol Chem. 272: 9221-9226.
17. Lau, S.Y., Kruck, T.P.A. and Sarker, B. (1974). Peptide molecule mimicking the copper (II) transport site of human serum albumin. J Biol Chem. 246, 5878-5884.
18. Linder, M.C. (1991). Biochemistry of copper. Biochemistry of the Elements. New York, Elsevier.
19. McArdle, H.J., Gross, S.M., Creaser, I., Sargeson, A.M. and Danks, D.M. (1989). The effect of chelators on copper metabolism and copper pools in mouse hepatocytes. Am. J. Physiol. 256, G667-G672.
20. McArdle, H.J., Gross, S.M. and Danks, D.M. (1988). Uptake of copper by mouse hepatocytes. J. Cell. Physiol. 136, 373-378.
21. McArdle, H.J., Gross, S.M., Danks, D.M. and Wedd, A.G. (1990a). Role of albumin's specific copper binding site in copper uptake by mouse hepatocytes. Am J Physiol. 258G, 988-991.
22. McArdle, H.J., Mercer, J.F., Sargeson, A.M. and Danks, D.M. (1990b). Effects of cellular copper content on copper uptake and metallothionein and ceruloplasmin mRNA in mouse hepatocytes. J. Nutr. 120, 1370-1375.
23. Morrissey, J.A., Williams, P.H. and Cashmore, A.M. (1996). Candida albicans has a cell-associated ferric-reductase activity which is regulated in response to levels of iron and copper. Microbiol. 142: 485-492.
24. Owen, C.A.J. (1980). Copper and hepatic function. Ciba Found Symp. 79, 267-82.
25. Petris, M.J., Mercer, J.F., Culvenor, J.G., Lockhart, P., Gleeson, P.A. and Camakaris, J. (1996). Ligand-regulated transport of the Menkes copper P-type ATPase efflux pump from the Golgi apparatus to the plasma membrane: a novel mechanism of regulated trafficking, EMBO. J>. 15, 6084-6095.
26. Petrovic, N., Comi, A. and Ettinger, M.J. (1997). Copper incorporation into superoxide dismutase in Menkes lymphoblasts. J. Biol. Chem. 271, 28335-28340.
27. Petrukhin, K., Lutsenko, S., Chernov, I., Ross, B.M., Kaplan, J.H. and Gilliam, T.C. (1994). Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing and structure/function predictions. Hum. Mol. Gen. 3, 1647-1656.
28. Schmitt, R.C., Darwish, H.M., Cheney, J.C. and Ettinger, M.J. (1983). Copper transport kinetics by isolated rat hepatocytes. Am. J. Physiol. 244, G183-G191.
29. Shatwell, K.P., Dancis, A., Cross, A.R. and Klausner, R.D. (1996). The FREI ferric reductase of Saccharomyces cerevisiae is a cytochrome b similar to that of NADPH oxidase. J Biol Chem. 271: 14240-14244.
30. Solioz, M., and Odermatt, A. (1995). Copper and silver transport by CopB-ATPase in membrane vesicles of Enterococcus hirae. J Biol Chem. 270: 9217-9221.
31. Sun, I.L., Navas, P., Crane, F.L., Morro, D.J. and Low, H. (1987). NADH diferric transferrin reductase in liver plasma membrane. J Biol Chem. 262, 15915-15921.
32. Tanzi, R.E., Petrukhin, K., Chernov, I., Pellequer, J.L., Wasco, W., Ross, B., Romano, D.M., Parano, E., Pavone, L., Brzustowicz, L.M., Devoto, M., Peppercorn, J., Bush, A.I., Sternlieb, I., Pirastu, M., Gusella, J.F., Evgrafov, O., Penchaszadeh, G.K., Honig, B., Edelman, I.S., Soares, M.B., Scheinberg, I.H. and Gilliam, T.C. (1993). The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene, Nature Genetics. 5, 344-350.
33. van den Berg, G.J. and McArdle, H.J. (1994). A plasma membrane NADH oxidase is involved in copper uptake by plasma membrane vesicles isolated from rat liver. Biochim. Biophys. Acta. 1195, 276-280.
34. Weiner, A.L. and Cousins, R.J. (1980). Copper accumulation and metabolism in primary monolayer culture of rat liver parenchymal cells. Biochim. Biophys. Acta. 629, 113-125.
35. Weiner, A.L. and Cousins, R.J. (1983). Hormonally produced changes in caeruloplasmin synthesis and secretion in primary cultured rat hepatocytes. Relationship to hepatic copper metabolism. Biochem. J. 212, 297-304.
36. Weiss, K.C., and Linder, M.C. (1985). Copper transport in rats involving a new plasma protein. Am J Physiol. 249: E77-E88.
37. Whitaker, P. and McArdle, H.J. (1997). Iron inhibits copper uptake by down-regulating the plasma membrane NADH oxidase. T.E.M.A. 9, 237-239.
38. Wilson, S.A.K. (1912). Progressive lenticular degeneration: A familial nervous disease associated with cirrhosis of the liver. Brain. 34, 295-509.
39. Wu, J., Forbes, J.R., Chen, H.S. and Cox, D.W. (1994). The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene. Nature Genetics. 7, 541-545.
40. Yang, X.L., Miura, N., Kawarada, Y., Terada, K., Petrukhin, K., Gilliam, T.C. and Sugiyama, T. (1997). Two forms of Wilson disease protein produced by alternative splicing are localized in distinct cellular compartments. Biochem. J. 326, 897-902.
41. Zaitseva, I., Zaitsev, V., Card, G., Moshkov, K., Bax, B., Ralph, A. and Lindley, P. (1996). The X-ray structure of human ceruloplasmin at 3.1 A: nature of the copper centres. J. Biol. Inorg. Chem. 1, 15-23.
42. Zhou, B. and Gitschier, J. (1997). hCTRl: A human gene for copper uptake identified by complementation in yeast. Proc. Natl. Acad. Sci. USA. 94, 7481-7486.