An ancient conserved role for prion protein in learning and memory

• Published in: Biology open 2018-01, Vol.7 (1), p.bio025734-bio025734
• Main Authors: Leighton, Patricia L A, Nadolski, Nathan J, Morrill, Adam, Hamilton, Trevor J, Allison, W Ted
• Format: Article
• Language: English
• Subjects: Age; Alzheimer; Alzheimer's disease; Animal models; Anxiety; Brain; Cognitive ability; Danio rerio; Dementia disorders; Diseases; Diving; Fish; Learning; Memory; Neurodegeneration; Neurodegenerative diseases; Novel object recognition; Object recognition; Oligomers; Pattern recognition; Prion protein; Protein folding; Proteins; Scrapie; Signs and symptoms; Synapses; Targeted Mutagenesis; Zebrafish
• ISSN: 2046-6390; 2046-6390
• DOI: 10.1242/bio.025734

The misfolding of cellular prion protein (PrP ) to form PrP Scrapie (PrP ) is an exemplar of toxic gain-of-function mechanisms inducing propagated protein misfolding and progressive devastating neurodegeneration. Despite this, PrP function in the brain is also reduced and subverted during prion disease progression; thus understanding the normal function of PrP in healthy brains is key. Disrupting PrP 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 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 in memory using a disparate animal model, the zebrafish. Here we document an age-dependent memory decline in zebrafish, pointing to a conserved and ancient role of PrP in memory. Specifically, we found that aged (3-year-old) fish performed poorly in an object recognition task relative to age-matched fish or 1-year-old fish. Further, using a novel object approach (NOA) test, we found that aged (3-year-old) fish approached the novel object more than either age-matched fish or 1-year-old 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 fish. The learning paradigm established here enables a path forward to study PrP 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 during Alzheimer's and prion diseases, and have implications upon the prospects of several promising therapeutic strategies.