a-Synuclein oligomers oppose long-term potentiation and impair memory through a calcineurin-dependent mechanism: relevance to human synucleopathic diseases

作者：Martin Zane S; Neugebauer Volker; Dineley Kelly T; Kayed Rakez; Zhang Wenru; Reese Lindsay C; Taglialatela Giulio^*

来源：Journal of Neurochemistry, 2012, 120(3): 440-452.

DOI：10.1111/j.1471-4159.2011.07576.x

• a-synuclein
• calcineurin
• DLB
• LTP
• memory
• oligomers

Intracellular deposition of fibrillar aggregates of a-synuclein (aSyn) characterizes neurodegenerative diseases such as Parkinsons disease (PD) and dementia with Lewy bodies. However, recent evidence indicates that small aSyn oligomeric aggregates that precede fibril formation may be the most neurotoxic species and can be found extracellularly. This new evidence has changed the view of pathological aSyn aggregation from a self-contained cellular phenomenon to an extracellular event and prompted investigation of the putative effects of extracellular aSyn oligomers. In this study, we report that extracellular application of aSyn oligomers detrimentally impacts neuronal welfare and memory function. We found that oligomeric aSyn increased intracellular Ca2+ levels, induced calcineurin (CaN) activity, decreased cAMP response element-binding protein (CREB) transcriptional activity and resulted in calcineurin-dependent death of human neuroblastoma cells. Similarly, CaN induction and CREB inhibition were observed when aSyn oligomers were applied to organotypic brain slices, which opposed hippocampal long-term potentiation. Furthermore, aSyn oligomers induced CaN, inhibited CREB and evoked memory impairments in mice that received acute intracerebroventricular injections. Notably, all these events were reversed by pharmacological inhibition of CaN. Moreover, we found decreased active CaN and reduced levels of phosphorylated CREB in autopsy brain tissue from patients affected by dementia with Lewy bodies, which is characterized by deposition of aSyn aggregates and progressive cognitive decline. These results indicate that exogenously applied aSyn oligomers impact neuronal function and produce memory deficits through mechanisms that involve CaN activation.

• 出版日期2012-2