http://www.cnr.it/ontology/cnr/individuo/prodotto/ID284056

Microglia convert aggregated amyloid-beta into neurotoxic forms through the shedding of microvesicles (Articolo in rivista)

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Microglia convert aggregated amyloid-beta into neurotoxic forms through the shedding of microvesicles (Articolo in rivista) (literal)

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Joshi, P.; Turola, E.; Ruiz, A.; Bergami, A.; Libera, D. D.; Benussi, L.; Giussani, P.; Magnani, G.; Comi, G.; Legname, G.; Ghidoni, R.; Furlan, R.; Matteoli, M.; Verderio, C. (2014)
Microglia convert aggregated amyloid-beta into neurotoxic forms through the shedding of microvesicles
in Cell death and differentiation
(literal)

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Joshi, P.; Turola, E.; Ruiz, A.; Bergami, A.; Libera, D. D.; Benussi, L.; Giussani, P.; Magnani, G.; Comi, G.; Legname, G.; Ghidoni, R.; Furlan, R.; Matteoli, M.; Verderio, C. (literal)

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University of Milan; CNR Inst Neurosci; Vita-Salute San Raffaele University; IRCCS Ist Ctr San Giovanni Dio Fatebenefratell; International School for Advanced Studies; IRCCS Humanitas (literal)

Titolo

Microglia convert aggregated amyloid-beta into neurotoxic forms through the shedding of microvesicles (literal)

Abstract

Alzheimer's disease (AD) is characterized by extracellular amyloid-beta (A beta) deposition, which activates microglia, induces neuroinflammation and drives neurodegeneration. Recent evidence indicates that soluble pre-fibrillar Ab species, rather than insoluble fibrils, are the most toxic forms of Ab. Preventing soluble Ab formation represents, therefore, a major goal in AD. We investigated whether microvesicles (MVs) released extracellularly by reactive microglia may contribute to AD degeneration. We found that production of myeloid MVs, likely of microglial origin, is strikingly high in AD patients and in subjects with mild cognitive impairment and that AD MVs are toxic for cultured neurons. The mechanism responsible for MV neurotoxicity was defined in vitro using MVs produced by primary microglia. We demonstrated that neurotoxicity of MVs results from (i) the capability of MV lipids to promote formation of soluble Ab species from extracellular insoluble aggregates and (ii) from the presence of neurotoxic A beta forms trafficked to MVs after A beta internalization into microglia. MV neurotoxicity was neutralized by the A beta-interacting protein PrP and anti-A beta antibodies, which prevented binding to neurons of neurotoxic soluble A beta species. This study identifies microglia-derived MVs as a novel mechanism by which microglia participate in AD degeneration, and suggest new therapeutic strategies for the treatment of the disease. (literal)

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