Literature DB >> 19233277

The effects of prion protein expression on metal metabolism.

Silvia Kralovicova1, Sarah N Fontaine, Alexandra Alderton, Julia Alderman, K Vala Ragnarsdottir, Steven J Collins, David R Brown.   

Abstract

The prion protein is a glycoprotein that binds metals such as copper and manganese. When converted to a proteinase resistant isoform it is associated with prion diseases such as Creutzfeldt-Jakob disease and bovine spongiform encephalopathy. Although, the co-ordination and metal affinity of the prion protein has been well studied, the association of the protein with cellular metal metabolism has been less well investigated. We used transgenic manipulation of prion protein expression and other recombinant techniques to alter expression of known copper binding proteins to investigate the role of the prion protein in copper metabolism. We found that changing the expression of the prion protein alters proteins associated with copper uptake, storage and export from the cell. In addition, alteration in the expression of superoxide dismutases increased prion protein expression dramatically. Reducing copper in the diet decreased expression of the prion protein in the brain while increased dietary manganese dramatically increased the protein's expression. Cellular prion infection also increased the expression of metal transporting proteins and increased cellular manganese concentrations. Overall our results show a close link between cellular resistance to oxidative stress and also copper metabolism. These findings are in line with previous data suggesting that the prion protein is an antioxidant and associated with copper uptake into cells. The disturbance to copper metabolism, as a result of altered prion protein expression clearly demonstrates the important role of the prion protein in copper metabolism. The implication is that prion protein expression has a homeostatic role in copper metabolism.

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Year:  2009        PMID: 19233277     DOI: 10.1016/j.mcn.2009.02.002

Source DB:  PubMed          Journal:  Mol Cell Neurosci        ISSN: 1044-7431            Impact factor:   4.314


  13 in total

1.  Activation and repression of prion protein expression by key regions of intron 1.

Authors:  Josephine A Wright; Patrick C McHugh; Mark Stockbridge; Samantha Lane; Silvia Kralovicova; David R Brown
Journal:  Cell Mol Life Sci       Date:  2009-12       Impact factor: 9.261

2.  Specificity protein 1 (sp1) oscillation is involved in copper homeostasis maintenance by regulating human high-affinity copper transporter 1 expression.

Authors:  Zheng D Liang; Wen-Bin Tsai; Mei-Yi Lee; Niramol Savaraj; Macus Tien Kuo
Journal:  Mol Pharmacol       Date:  2011-12-15       Impact factor: 4.436

Review 3.  Manganese (Mn) and iron (Fe): interdependency of transport and regulation.

Authors:  Vanessa A Fitsanakis; Na Zhang; Stephanie Garcia; Michael Aschner
Journal:  Neurotox Res       Date:  2009-11-18       Impact factor: 3.911

4.  Na+/K+-ATPase is present in scrapie-associated fibrils, modulates PrP misfolding in vitro and links PrP function and dysfunction.

Authors:  James F Graham; Dominic Kurian; Sonya Agarwal; Lorna Toovey; Lawrence Hunt; Louise Kirby; Teresa J T Pinheiro; Steven J Banner; Andrew C Gill
Journal:  PLoS One       Date:  2011-11-02       Impact factor: 3.240

Review 5.  Antioxidant and Metal Chelation-Based Therapies in the Treatment of Prion Disease.

Authors:  Marcus W Brazier; Anthony G Wedd; Steven J Collins
Journal:  Antioxidants (Basel)       Date:  2014-04-21

Review 6.  Selective vulnerability to neurodegenerative disease: the curious case of Prion Protein.

Authors:  Walker S Jackson
Journal:  Dis Model Mech       Date:  2014-01       Impact factor: 5.758

Review 7.  Isoprostanes and neuroprostanes as biomarkers of oxidative stress in neurodegenerative diseases.

Authors:  Elżbieta Miller; Agnieszka Morel; Luciano Saso; Joanna Saluk
Journal:  Oxid Med Cell Longev       Date:  2014-04-29       Impact factor: 6.543

Review 8.  Prion protein and aging.

Authors:  Lisa Gasperini; Giuseppe Legname
Journal:  Front Cell Dev Biol       Date:  2014-08-29

9.  Manganese enhances prion protein survival in model soils and increases prion infectivity to cells.

Authors:  Paul Davies; David R Brown
Journal:  PLoS One       Date:  2009-10-21       Impact factor: 3.240

10.  Dietary magnesium and copper affect survival time and neuroinflammation in chronic wasting disease.

Authors:  Tracy A Nichols; Terry R Spraker; Thomas Gidlewski; Bruce Cummings; Dana Hill; Qingzhong Kong; Aru Balachandran; Kurt C VerCauteren; Mark D Zabel
Journal:  Prion       Date:  2016-05-03       Impact factor: 3.931

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