Evidence map›Paper›PMID 40888514›Full record

ArticleJournal of Alzheimer's disease : JAD2025

Phosphorylation at serine 214 correlates with tau seeding activity in an age-dependent manner in two mouse models for tauopathies and is required for tau transsynaptic propagation.

Pablo Martinez, Nur Jury-Garfe, Henika Patel, Yanwen You, Abigail Perkins, Yingjian You, Audrey Lee-Gosselin, Ruben Vidal, Cristian A Lasagna-Reeves

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Pablo MartinezDepartment of Neurology, Baylor College of Medicine, Houston, TX, USA.
Nur Jury-GarfeDepartment of Neurology, Baylor College of Medicine, Houston, TX, USA.
Henika PatelDepartment of Neurology, Baylor College of Medicine, Houston, TX, USA.
Yanwen YouStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Abigail PerkinsStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Yingjian YouStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Audrey Lee-GosselinStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Ruben VidalStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Cristian A Lasagna-ReevesDepartment of Neurology, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0002-5499-3082

Funding

Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
Tau-seed protein interactome and its role in neurodegenerative tauopathiesR01NS119280 · NINDS · INDIANA UNIVERSITY INDIANAPOLIS · PI LASAGNA-REEVES, CRISTIAN · 2020 to 2024
$3.5M
CAA, Tau and NeurodegenerationRF1AG059639 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI LASAGNA-REEVES, CRISTIAN · 2024 to 2024
$2.3M
NCATS NIH HHS UL1 TR002529NIA NIH HHS RF1 AG059639NINDS NIH HHS R01 NS119280
6 · The paper itself

Abstract

BackgroundTau aggregation and propagation are hallmark features of Alzheimer's disease and related tauopathies. The molecular identity and post-translational modifications that contribute to tau seeding activity remain incompletely understood.ObjectiveTo characterize the temporal dynamics of tau seeding activity and identify specific phosphorylated tau species associated with tau propagation in vivo.MethodsWe profiled tau seeding activity using a FRET-based biosensor cell line and correlated it with the abundance of phospho- and conformational tau species in two transgenic mouse models of tauopathy (P301S-1N4R and P301S-0N4R). Immunohistochemistry and subcellular fractionation were used to examine the spatial distribution of tau species. Functional relevance of serine 214 phosphorylation was assessed via phospho-dead mutants in

Indexed as

SerineTauopathiestau ProteinsAge FactorsAnimalsBrainDisease Models, AnimalDrosophilaHumansMiceMice, Inbred C57BLMice, TransgenicNeuronsPhosphorylationSerinetau ProteinsAlzheimer's diseasepropagationtautau phosphorylation

Identifiers

PMID40888514
PMCPMC12495114

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.