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The Anti-Prion Antibody 15B3 Detects Toxic Amyloid-β Oligomers

15B3 is a monoclonal IgM antibody that selectively detects pathological aggregates of the prion protein (PrP). We report the unexpected finding that 15B3 also recognizes oligomeric but not monomeric forms of amyloid-β (Aβ)(42), an aggregating peptide implicated in the pathogenesis of Alzheimer’s dis...

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Detalles Bibliográficos
Autores principales: Stravalaci, Matteo, Tapella, Laura, Beeg, Marten, Rossi, Alessandro, Joshi, Pooja, Pizzi, Erika, Mazzanti, Michele, Balducci, Claudia, Forloni, Gianluigi, Biasini, Emiliano, Salmona, Mario, Diomede, Luisa, Chiesa, Roberto, Gobbi, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5044783/
https://www.ncbi.nlm.nih.gov/pubmed/27392850
http://dx.doi.org/10.3233/JAD-150882
Descripción
Sumario:15B3 is a monoclonal IgM antibody that selectively detects pathological aggregates of the prion protein (PrP). We report the unexpected finding that 15B3 also recognizes oligomeric but not monomeric forms of amyloid-β (Aβ)(42), an aggregating peptide implicated in the pathogenesis of Alzheimer’s disease (AD). The 15B3 antibody: i) inhibits the binding of synthetic Aβ(42) oligomers to recombinant PrP and neuronal membranes; ii) prevents oligomer-induced membrane depolarization; iii) antagonizes the inhibitory effects of oligomers on the physiological pharyngeal contractions of the nematode Caenorhabditis elegans; and iv) counteracts the memory deficits induced by intracerebroventricular injection of Aβ(42) oligomers in mice. Thus this antibody binds to pathologically relevant forms of Aβ, and offers a potential research, diagnostic, and therapeutic tool for AD.