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In vivo hyperphosphorylation of tau is associated with synaptic loss and behavioral abnormalities in the absence of tau seeds.

Authors :
Watamura N
Foiani MS
Bez S
Bourdenx M
Santambrogio A
Frodsham C
Camporesi E
Brinkmalm G
Zetterberg H
Patel S
Kamano N
Takahashi M
Rueda-Carrasco J
Katsouri L
Fowler S
Turkes E
Hashimoto S
Sasaguri H
Saito T
Islam AS
Benner S
Endo T
Kobayashi K
Ishida C
Vendruscolo M
Yamada M
Duff KE
Saido TC
Source :
Nature neuroscience [Nat Neurosci] 2025 Feb; Vol. 28 (2), pp. 293-307. Date of Electronic Publication: 2024 Dec 24.
Publication Year :
2025

Abstract

Tau pathology is a hallmark of several neurodegenerative diseases, including frontotemporal dementia and Alzheimer's disease. However, the sequence of events and the form of tau that confers toxicity are still unclear, due in large part to the lack of physiological models of tauopathy initiation and progression in which to test hypotheses. We have developed a series of targeted mice expressing frontotemporal-dementia-causing mutations in the humanized MAPT gene to investigate the earliest stages of tauopathy. MAPT <superscript>Int10+3G>A</superscript> and MAPT <superscript>S305N;Int10+3G>A</superscript> lines show abundant hyperphosphorylated tau in the hippocampus and entorhinal cortex, but they do not develop seed-competent fibrillar structures. Accumulation of hyperphosphorylated tau was accompanied by neurite degeneration, loss of viable synapses and indicators of behavioral abnormalities. Our results demonstrate that neuronal toxicity can occur in the absence of fibrillar, higher-order structures and that tau hyperphosphorylation is probably involved in the earliest etiological events in tauopathies showing isoform ratio imbalance.<br />Competing Interests: Competing interests: T.E. serves as a Representative for Phenovance LLC, which provides commercial service using IntelliCage. T.C.S. serves as an Executive Consultant for RIKEN BIO Co. Ltd., which sublicenses App knock-in mice to for-profit organizations. K.E.D. is a board member of Ceracuity LLC. H.Z. has served at scientific advisory boards and/or as a consultant for Abbvie, Acumen, Alector, Alzinova, ALZPath, Annexon, Apellis, Artery Therapeutics, AZTherapies, CogRx, Denali, Eisai, Nervgen, Novo Nordisk, Optoceutics, Passage Bio, Pinteon Therapeutics, Prothena, Red Abbey Labs, reMYND, Roche, Samumed, Siemens Healthineers, Triplet Therapeutics and Wave, has given lectures in symposia sponsored by Cellectricon, Fujirebio, Alzecure, Biogen and Roche, and is a cofounder of Brain Biomarker Solutions in Gothenburg AB (BBS), which is a part of the GU Ventures Incubator Program (outside submitted work). The other authors declare no competing interests.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1546-1726
Volume :
28
Issue :
2
Database :
MEDLINE
Journal :
Nature neuroscience
Publication Type :
Academic Journal
Accession number :
39719507
Full Text :
https://doi.org/10.1038/s41593-024-01829-7