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Article type: Short Communication
Authors: Berry, Alessandraa; 1 | Vacirca, Davidea; 1 | Capoccia, Saraa | Bellisario, Veronicaa | Malorni, Walterb; c | Ortona, Elenaa; b; 2; * | Cirulli, Francescaa; 2
Affiliations: [a] Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome, Italy | [b] San Raffaele Institute Sulmona, Sulmona (AQ), Italy | [c] Department of Therapeutic Research and Medicine Evaluation, Istituto Superiore di Sanità, Rome, Italy
Correspondence: [*] Correspondence to: Dr. Elena Ortona, Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome, Italy. Tel.: +39 0649902573; Fax: +39 0649902040; E-mail: elena.ortona@iss.it.
Note: [1] These authors contributed equally to this work.
Note: [2] Both considered as senior authors.
Abstract: Previous studies have suggested a pathogenetic role of autoantibodies (Abs) against ATP synthase (ATPs) in patients with Alzheimer's disease (AD). Using a mouse model, we found that intracerebroventricular administration of anti-ATPs-Abs, purified from AD patients, leads to poor cognitive performance and pronounced cell damage in the hippocampus, a brain region specifically involved in learning and memory processes, which is severely affected in AD. Our results are suggestive of a role of anti-ATPs-Abs in the onset and progression of AD and also provide a fruitful model for the study of memory disturbances in neurodegenerative diseases.
Keywords: Alzheimer's disease, apoptosis, ATP synthase, autoantibodies, maze learning, memory, mice
DOI: 10.3233/JAD-2012-121312
Journal: Journal of Alzheimer's Disease, vol. 33, no. 2, pp. 317-321, 2013
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