N-terminal heterogeneity of parenchymal and vascular amyloid-β deposits in Alzheimer's disease.


Journal

Neuropathology and applied neurobiology
ISSN: 1365-2990
Titre abrégé: Neuropathol Appl Neurobiol
Pays: England
ID NLM: 7609829

Informations de publication

Date de publication:
12 2020
Historique:
received: 31 01 2020
accepted: 24 05 2020
pubmed: 5 6 2020
medline: 29 10 2021
entrez: 5 6 2020
Statut: ppublish

Résumé

The deposition of amyloid-β (Aβ) peptides in the form of extracellular plaques in the brain represents one of the classical hallmarks of Alzheimer's disease (AD). In addition to 'full-length' Aβ starting with aspartic acid (Asp-1), considerable amounts of various shorter, N-terminally truncated Aβ peptides have been identified by mass spectrometry in autopsy samples from individuals with AD. Selectivity of several antibodies detecting full-length, total or N-terminally truncated Aβ species has been characterized with capillary isoelectric focusing assays using a set of synthetic Aβ peptides comprising different N-termini. We further assessed the N-terminal heterogeneity of extracellular and vascular Aβ peptide deposits in the human brain by performing immunohistochemical analyses using sporadic AD cases with antibodies targeting different N-terminal residues, including the biosimilar antibodies Bapineuzumab and Crenezumab. While antibodies selectively recognizing Aβ In contrast to other studied Aβ

Identifiants

pubmed: 32497293
doi: 10.1111/nan.12637
pmc: PMC8082844
mid: NIHMS1615734
doi:

Substances chimiques

Amyloid beta-Peptides 0
Antibodies, Monoclonal, Humanized 0
Peptide Fragments 0
bapineuzumab NC11WKO35D

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

673-685

Subventions

Organisme : NIA NIH HHS
ID : RF1 AG059695
Pays : United States

Informations de copyright

© 2020 The Authors. Neuropathology and Applied Neurobiology published by John Wiley & Sons Ltd on behalf of British Neuropathological Society.

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Auteurs

S Zampar (S)

Department of Psychiatry and Psychotherapy, University Medical Center (UMG), Georg-August-University, Göttingen, Germany.

H W Klafki (HW)

Department of Psychiatry and Psychotherapy, University Medical Center (UMG), Georg-August-University, Göttingen, Germany.

K Sritharen (K)

Department of Psychiatry and Psychotherapy, University Medical Center (UMG), Georg-August-University, Göttingen, Germany.

T A Bayer (TA)

Department of Psychiatry and Psychotherapy, University Medical Center (UMG), Georg-August-University, Göttingen, Germany.

J Wiltfang (J)

Department of Psychiatry and Psychotherapy, University Medical Center (UMG), Georg-August-University, Göttingen, Germany.
Neurosciences and Signaling Group, Department of Medical Sciences, Institute of Biomedicine (iBiMED), University of Aveiro, Aveiro, Portugal.
German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.

A Rostagno (A)

Departments of, Pathology, New York University School of Medicine, New York, NY, USA.

J Ghiso (J)

Departments of, Pathology, New York University School of Medicine, New York, NY, USA.
Department of, Psychiatry, New York University School of Medicine, New York, NY, USA.

L A Miles (LA)

St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.

O Wirths (O)

Department of Psychiatry and Psychotherapy, University Medical Center (UMG), Georg-August-University, Göttingen, Germany.

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Classifications MeSH