Soluble prion protein and its N-terminal fragment prevent impairment of synaptic plasticity by Aβ oligomers: Implications for novel therapeutic strategy in Alzheimer's disease

NEUROBIOLOGY OF DISEASE

卷:91

Article

Scott-McKean, Jonah J.¹  Surewicz, Krystyna²  Choi, Jin-Kyu²  Ruffin, Vernon A.^2,5  Salameh, Ahlam I.²  Nieznanski, Krzysztof⁴  Costa, Alberto C. S.^1,3  Surewicz, Witold K.² 

[1] Case Western Reserve Univ, Div Pediat Neurol, Dept Pediat, Cleveland, OH 44116 USA

[2] Case Western Reserve Univ, Dept Physiol & Biophys, Cleveland, OH 44116 USA

[3] Case Western Reserve Univ, Dept Psychiat, Cleveland, OH 44116 USA

[4] M Nencki Inst Expt Biol, Dept Biochem, PL-02093 Warsaw, Poland

[5] Virginia Union Univ, Dept Nat Resources, Richmond, VA USA

关键词: Alzheimer's disease;    Amyloid-beta (A beta);    Prion protein;    Synaptic plasticity;    Long-term potentiation;    Cytotoxicity;   

DOI  :  10.1016/j.nbd.2016.03.001

来源: Elsevier

【 摘 要 】

The pathogenic process in Alzheimer's disease (AD) appears to be closely linked to the neurotoxic action of amyloid-beta (A beta) oligomers. Recent studies have shown that these oligomers bind with high affinity to the membrane-anchored cellular prion protein (PrPc). It has also been proposed that this binding might mediate some of the toxic effects of the oligomers. Here, we show that the soluble (membrane anchor-free) recombinant human prion protein (rPrP) and its N-terminal fragment N1 block A beta oligomers-induced inhibition of long-term potentiation (LTP) in hippocampal slices, an important surrogate marker of cognitive deficit associated with AD. rPrP and N1 are also strikingly potent inhibitors of Ala cytotoxicity in primary hippocampal neurons. Furthermore, experiments using hippocampal slices and neurons from wild-type and PrPc null mice (as well as rat neurons in which PrPc expression was greatly reduced by gene silencing) indicate that, in contrast to the impairment of synaptic plasticity by A beta oligomers, the cytotoxic effects of these oligomers, and the inhibition of these effects by rPrP and N1, are independent of the presence of endogenous PrPc. This suggests fundamentally different mechanisms by which soluble rPrP and its fragments inhibit these two toxic responses to A beta. Overall, these findings provide strong support to recent suggestions that PrP-based compounds may offer new avenues for pharmacological intervention in AD. (C) 2016 Elsevier Inc. All rights reserved.

【 授权许可】

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