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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2016
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Stravalaci, Matteo |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5044783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50447832016-10-04 The Anti-Prion Antibody 15B3 Detects Toxic Amyloid-β Oligomers 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 J Alzheimers Dis Research Article 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. IOS Press 2016-08-08 /pmc/articles/PMC5044783/ /pubmed/27392850 http://dx.doi.org/10.3233/JAD-150882 Text en IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article 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 The Anti-Prion Antibody 15B3 Detects Toxic Amyloid-β Oligomers |
title | The Anti-Prion Antibody 15B3 Detects Toxic Amyloid-β Oligomers |
title_full | The Anti-Prion Antibody 15B3 Detects Toxic Amyloid-β Oligomers |
title_fullStr | The Anti-Prion Antibody 15B3 Detects Toxic Amyloid-β Oligomers |
title_full_unstemmed | The Anti-Prion Antibody 15B3 Detects Toxic Amyloid-β Oligomers |
title_short | The Anti-Prion Antibody 15B3 Detects Toxic Amyloid-β Oligomers |
title_sort | anti-prion antibody 15b3 detects toxic amyloid-β oligomers |
topic | Research Article |
url | 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 |
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