Decreased brain copper due to copper deficiency has no effect on bovine prion proteins

Biochemical and Biophysical Research Communications

Volumn 352, Issue 4, 2007, Pages 884-888

  Legleiter, Leon R ^a   Ahola, Jason K ^b   Engle, Terry E ^b   Spears, Jerry W ^a  

^a NORTH CAROLINA STATE UNIVERSITY   (United States)

^b Department of Environmental and Radiological Health Sciences   (United States)

Author keywords

Bovine; Bovine spongiform encephalopathy; Brain; Copper; Copper deficiency; Prion protein

Indexed keywords

COPPER; PRION PROTEIN; PROTEINASE; PROTEINASE K;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BOVINE SPONGIFORM ENCEPHALOPATHY; BRAIN LEVEL; CONTROLLED STUDY; COPPER DEFICIENCY; COW; ELUTION; ENZYME DEGRADATION; MOLECULAR WEIGHT; NONHUMAN; PRION DISEASE; PRIORITY JOURNAL; WESTERN BLOTTING;

ANIMALS; BRAIN; CATTLE; COPPER; MANGANESE; MOLECULAR WEIGHT; PRION DISEASES; PRIONS; SUPEROXIDE DISMUTASE;

BOS TAURUS;

EID: 33845398133     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2006.11.108     Document Type: Article

References (35)

1. Prusiner S.B. Novel proteinaceous infectious particles cause scrapie. Science 216 (1982) 136-144
2. Collinge J. Molecular neurology of prion disease. J. Neurol. Neurosurg. Psychiatry 76 (2005) 906-919
3. Prusiner S.B. Prion Biology and Disease (2004), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York
4. Prusiner S.B., Scott M.R., Dearmond S.J., and Cohen F.E. Prion protein biology. Cell 93 (1998) 337-348
5. Brown D.R., Hafiz F., Glasssmith L.L., Wong B.S., Jones I.M., Clive C., and Haswell S.J. Consequences of manganese replacement of copper for prion protein function and proteinase resistance. EMBO J. 19 (2000) 1180-1186
6. Brown D.R. Copper and prion disease. Brain Res. Bull. 55 (2001) 165-173
7. Deloncle R., Guillard O., Bind J.L., Delaval J., Fleury N., Mauco G., and Lesage G. Free radical generation of protease-resistant prion after substitution of manganese for copper in bovine brain homogenate. Neurotoxicology 27 (2006) 437-444
8. Brown D.R., Qin K., Herms J.W., Madlung A., Manson J., Strome R., Fraser P.E., Kruck T., Bohlem A.V., Schulz-Schaeffer W., Giese A., Westaway D., and Kretzschmar H. The cellular prion protein binds copper in vivo. Nature 390 (1997) 684-687
9. Brown D.R. Prion protein expression aids cellular uptake and veratridine-induced release of copper. J. Neurosci. Res. 58 (1999) 717-725
10. Kramer M.L., Kratzin H.D., Schmidt B., Romer A., Windi O., Liemann S., Hornemann S., and Kretzschmar H. Prion protein binds copper within the physiological concentration range. J. Biol. Chem. 276 (2001) 16711-16719
11. Hornshaw M.P., McDermott J.R., and Candy J.M. Copper binding to the N-terminal tandem repeat regions of mammalian and avian prion protein. Biochem. Biophys. Res. Commun. 207 (1995) 621-629
12. Hornshaw M.P., McDermott J.R., Candy J.M., and Lakey J.H. Copper binding to the N-terminal tandem repeat region of mammalian and avian prion protein: structural studies using synthetic peptides. Biochem. Biophys. Res. Commun. 214 (1995) 993-999
13. Lehmann S. Metal ions and prion diseases. Curr. Opin. Chem. Biol. 6 (2002) 187-192
14. Brown D.R., Wong B.S., Hafiz F., Clive C., Haswell S.J., and Jones I.M. Normal prion protein has an activity like that of superoxide dismutase. Biochem. J. 344 (1999) 1-5
15. Martins V.R., and Brentani R.R. The biology of the cellular prion protein. Neurochem. Int. 41 (2002) 353-355
16. Brown D.R., Schulz-Schaeffer W.J., Schmidt B., and Kretzschmar H.A. Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity. Exp. Neurol. 146 (1997) 104-112
17. Wong B.S., Pan T., Liu T., Li R., Gambetti P., and Sy M.S. Differential contribution of superoxide dismutase activity by prion protein in vivo. Biochem. Biophys. Res. Commun. 273 (2000) 136-139
18. Tsenkova R.N., Iordanova I.K., Toyoda K., and Brown D.R. Prion protein fate governed by metal binding. Biochem. Biophys. Res. Commun. 325 (2004) 1005-1012
19. Wong B.S., Chen S.G., Colucci M., Xie Z., Pan T., Liu T., Li R., Gambetti P., Sy M.S., and Brown D.R. Aberrant metal binding by prion protein in human prion disease. J. Neurochem. 78 (2001) 1400-1408
20. Wong B.S., Brown D.R., Pan T., Whiteman M., Liu T., Bu X., Li R., Gambetti P., Olesik J., Rubenstein R., and Sy M.S. Oxidative impairment in scrapie-infected mice is associated with brain metals perturbations and altered antioxidant activities. J. Neurochem. 79 (2001) 689-698
21. Thackray A.M., Knight R., Haswell S.J., Bujdoso R., and Brown D.R. Metal imbalance and compromised antioxidant function are early changes in prion disease. Biochem. J. 362 (2002) 253-258
22. Underwood E.J., and Suttle N.F. The mineral nutrition of livestock. 3rd ed. (1999), Commonwealth Agric. Bureaux, Slough, U.K.
23. Pearson E.G., and Craig A.M. The diagnosis of liver disease in equine and food animals. Mod. Vet. Pract. 61 (1980) 233-237
24. Engle T.E., and Spears J.W. Effects of dietary copper concentration and source on performance and copper status of growing and finishing steers. J. Anim. Sci. 78 (2000) 2446-2451
25. Mills C.F. Biochemical and biophysical indicators of mineral status in animals: copper, cobalt, and zinc. J. Anim. Sci. 65 (1987) 1702-1711
26. NRC, Nutrient Requirements of Domestic Animals, Nutrient Requirements of Beef Cattle, 7th Ed., Natl. Acad. Press, Washington, DC., 1996.
27. Engle T.E., Nockels C.F., Kimberling C.V., Weaber D.L., and Johnson A.B. Zinc repletion with organic or inorganic forms of zinc and protein turnover in marginally zinc-deficient calves. J. Anim. Sci. 75 (1997) 3074-3081
28. Gengelbach G.P., Ward J.D., and Spears J.W. Effect of dietary copper, iron and molybdenum on growth and copper status of beef cows and calves. J. Anim. Sci. 72 (1997) 2722-2727
29. Suttle N.F., and Angus K.W. Experimental copper deficiency in the calf. J. Comp. Pathol. 86 (1976) 595-608
30. Suttle N.F., and Field A.C. Effect of intake of copper, molybdenum and sulphate on copper metabolism in sheep. J. Comp. Pathol. 79 (1969) 453-464
31. Suttle N.F., Field A.C., and Barlow R.M. Experimental copper deficiency in sheep. J. Comp. Pathol. 80 (1970) 151-162
32. Moudjou M., Frobert Y., Grassi J., and Bonnardiere C.L. Cellular prion protein status in sheep: tissue-specific biochemical signatures. J. Gen. Virol. 82 (2001) 2017-2024
33. Waggoner D.J., Drisaldi B., Bartnikas T.B., Casareno R.L.B., Prohaska J.R., Gitlin J.D., and Harris D.A. Brain copper content and cuproenzyme activity do not vary with prion protein expression level. J. Biol. Chem. 275 (2000) 7455-7458
34. Jones S., Batchelor M., Bhelt D., Clarke A.R., Collinge J., and Jackson G.S. Recombinant prion protein does not possess SOD-1 activity. Biochem. J. 392 (2005) 309-312
35. Hutter G., Heppner F.L., and Aguzzi A. No superoxide dismutase activity of cellular prion protein in vivo. Biol. Chem. 384 (2003) 1279-1285