Prion protein facilitates uptake of zinc into neuronal cells

Nicole T. Watt, David R. Taylor, Talitha L. Kerrigan, Heledd H. Griffiths, Jo V. Rushworth, Isobel J. Whitehouse, Nigel M. Hooper

    Research output: Contribution to journalArticlepeer-review


    Zinc is released into the synaptic cleft upon exocytotic stimuli, although the mechanism for its reuptake into neurons is unresolved. Here we show that the cellular prion protein enhances the uptake of zinc into neuronal cells. This prion-protein-mediated zinc influx requires the octapeptide repeats and amino-terminal polybasic region in the prion protein, but not its endocytosis. Selective antagonists of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) receptors block the prion protein-mediated zinc uptake, and the prion protein co-immunoprecipitates with both GluA1 and GluA2 AMPA receptor subunits. Zinc-sensitive intracellular tyrosine phosphatase activity is decreased in cells expressing prion protein and increased in the brains of prion-protein-null mice, providing evidence of a physiological consequence of this process. Prion protein-mediated zinc uptake is ablated in cells expressing familial associated mutants of the protein and in prion-infected cells. These data suggest that alterations in the cellular prion protein-mediated zinc uptake may contribute to neurodegeneration in prion and other neurodegenerative diseases. © 2012 Macmillan Publishers Limited. All rights reserved.
    Original languageEnglish
    Article number1134
    JournalNature Communications
    Publication statusPublished - 2012

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