Journal
BRAIN RESEARCH
Volume 1471, Issue -, Pages 102-117Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.brainres.2012.06.025
Keywords
Alzheimer's disease; Parkinson's disease; Pepstatin A; Chloroquine; Lysosome
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Funding
- San Paolo (Project Neuroscienze) [2008.2395]
- Regione Piemonte (Fticerca Sanitaria Finalizzata, Torino)
- Consorzio InterUniversitario per le Biotecnologie (CIB, Trieste)
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A pathological hallmark of Alzheimer's disease (AD) is the presence within neurons and the interneuronal space of aggregates of beta-amyloid (A beta) peptides that originate from an abnormal proteolytic processing of the amyloid precursor protein (APP). The aspartyl proteases that initiate this processing act in the Golgi and endosomal compartments. Here, we show that the neurotransmitter dopamine stimulates the rapid endocytosis and processing of APP and induces apoptosis in neuroblastoma Neuro2A cells over-expressing transgenic human APP (Swedish mutant). Apoptosis could be prevented by impairing Pepstatin-sensitive and acid-dependent proteolysis of APP within endosomal-lysosomal compartments. The gamma-secretase inhibitor L685,458 and the alpha-secretase stimulator phorbol ester elicited protection from dopamine-induced proteolysis of APP and cell toxicity. Our data shed lights on the mechanistic link between dopamine excitotoxicity, processing of APP and neuronal cell death. Since AD often associates with parkinsonian symptoms, which is suggestive of dopaminergic neurodegeneration, the present data provide the rationale for the therapeutic use of lysosomal activity inhibitors such as chloroquine or Pepstatin A to alleviate the progression of AD leading to onset of parkinsonism. (c) 2012 Elsevier B.V. All rights reserved.
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