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An ancient conserved role for prion protein in learning and memory
Author(s) -
Patricia L.A. Leighton,
Nathan J. Nadolski,
Adam Morrill,
Trevor J. Hamilton,
W. Ted Allison
Publication year - 2018
Publication title -
biology open
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.936
H-Index - 41
ISSN - 2046-6390
DOI - 10.1242/bio.025734
Subject(s) - biology , zebrafish , neurodegeneration , neuroscience , memory impairment , disease , fish <actinopterygii> , cognition , vertebrate , function (biology) , evolutionary biology , genetics , pathology , gene , medicine , fishery
The misfolding of cellular prion protein (PrP C ) to form PrP Scrapie (PrP Sc ) is an exemplar of toxic gain-of-function mechanisms inducing propagated protein misfolding and progressive devastating neurodegeneration. Despite this, PrP C function in the brain is also reduced and subverted during prion disease progression; thus understanding the normal function of PrP C in healthy brains is key. Disrupting PrP C in mice has led to a myriad of controversial functions that sometimes map onto disease symptoms, including a proposed role in memory or learning. Intriguingly, PrP C interaction with amyloid beta (Aβ) oligomers at synapses has also linked its function to Alzheimer's disease and dementia in recent years. We set out to test the involvement of PrP C in memory using a disparate animal model, the zebrafish. Here we document an age-dependent memory decline in prp2 -/- zebrafish, pointing to a conserved and ancient role of PrP C in memory. Specifically, we found that aged (3-year-old) prp2 -/- fish performed poorly in an object recognition task relative to age-matched prp2 +/+ fish or 1-year-old prp2 -/- fish. Further, using a novel object approach (NOA) test, we found that aged (3-year-old) prp2 -/- fish approached the novel object more than either age-matched prp2 +/+ fish or 1-year-old prp2 -/- fish, but did not have decreased anxiety when we tested them in a novel tank diving test. Taken together, the results of the NOA and novel tank diving tests suggest an altered cognitive appraisal of the novel object in the 3-year-old prp2 -/- fish. The learning paradigm established here enables a path forward to study PrP C interactions of relevance to Alzheimer's disease and prion diseases, and to screen for candidate therapeutics for these diseases. The findings underpin a need to consider the relative contributions of loss- versus gain-of-function of PrP C during Alzheimer's and prion diseases, and have implications upon the prospects of several promising therapeutic strategies.

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