Evidence map›Paper›PMID 36344699›Full record

ArticleNature neuroscience2022

Bassoon contributes to tau-seed propagation and neurotoxicity.

Pablo Martinez, Henika Patel, Yanwen You, Nur Jury, Abigail Perkins, Audrey Lee-Gosselin, Xavier Taylor, Yingjian You, Gonzalo Viana Di Prisco, Xiaoqing Huang and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Nature neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
7.2field-weighted citation impact, top 2% of its field
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

42 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Mitochondrial NADK2-dependent NADPH controls tau oligomer uptake in human neurons.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. CRISPR-edited iPSCs reveal BSN gene mutations induce neuronal hyperexcitability via astrocyte lipid accumulation.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Longitudinal tau aggregation, atrophy, and cognitive decline in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  18. Review
  19. ApoE3 Christchurch and tau interaction as a protective mechanism against Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors at 3 institutions in 1 country.

Pablo MartinezStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Henika PatelStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Yanwen YouStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Nur JuryStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Abigail PerkinsStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID http://orcid.org/0000-0001-7562-1635
Audrey Lee-GosselinStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Xavier TaylorStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Yingjian YouStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Gonzalo Viana Di PriscoStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Xiaoqing HuangDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA.
Sayan DuttaDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN, USA.
Aruna B WijeratneDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID http://orcid.org/0000-0001-8366-2074
Javier Redding-OchoaDivision of Neuropathology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Syed Salman ShahidStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID http://orcid.org/0000-0002-0914-6933
Juan F CodocedoStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Sehong MinDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN, USA.ORCID http://orcid.org/0000-0002-4511-850X
Gary E LandrethStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Amber L MosleyDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID http://orcid.org/0000-0001-5822-2894
Yu-Chien WuStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
David L McKinzieStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
Jean-Christophe RochetDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN, USA.ORCID http://orcid.org/0000-0002-6484-1541
Jie ZhangCenter for Computational Biology and Bioinformatics, Indiana University School of Medicine, Indianapolis, IN, USA.
Brady K AtwoodStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID http://orcid.org/0000-0002-7441-2724
Juan TroncosoDivision of Neuropathology, Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Cristian A Lasagna-ReevesStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA. clasagna@iu.edu.ORCID http://orcid.org/0000-0002-5499-3082
Indiana University School of MedicinePurdue University West Lafayette · USJohns Hopkins University · US

Funding

Project 2 MeasurementU19AG033655 · NIA · JOHNS HOPKINS UNIVERSITY · PI MARILYN S. ALBERT · 2014 to 2026
$51.5M
Understanding Mechanisms of a-synuclein pathologyP50NS038377 · NINDS · JOHNS HOPKINS UNIVERSITY · PI DAWSON, TED M. · 1998 to 2019
$38.8M
Research Education ComponentP30AG066507 · NIA · JOHNS HOPKINS UNIVERSITY · PI MARILYN S. ALBERT · 2020 to 2026
$29.3M
Tau-seed protein interactome and its role in neurodegenerative tauopathiesR01NS119280 · NINDS · INDIANA UNIVERSITY INDIANAPOLIS · PI LASAGNA-REEVES, CRISTIAN · 2020 to 2024
$3.5M
Comprehensive identification and validation of immune and inflammatory signatures associated to Cerebral Amyloid Angiopathy (CAA) utilizing the NanoString technology.R01AG059639 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI LASAGNA-REEVES, CRISTIAN · 2018 to 2022
$3.1M
Comprehensive White-matter Microstructure-informed Analytical Methods to Elucidate Neurobiological Mechanisms of Sports-related Concussion (SRC)R01NS112303 · NINDS · INDIANA UNIVERSITY INDIANAPOLIS · PI HAREZLAK, JAROSLAW, WU, YU-CHIEN · 2020 to 2024
$2.3M
Modeling Axonal Density and Inflammation-Associated Cellularity in Alzheimer’s Disease Using Hybrid Diffusion ImagingR01AG053993 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI WU, YU-CHIEN · 2016 to 2020
$2.0M
Identify and study the roles of key genes and proteins in subpopulations of Alzheimer's disease patients with uncoupled neurofibrillary tanglesR21AG075541 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI ZHANG, JIE · 2022 to 2022
$426k
NIA NIH HHS P30 AG066507NIA NIH HHS R01 AG053993NIA NIH HHS R01 AG059639NIA NIH HHS R21 AG075541NIA NIH HHS U19 AG033655NINDS NIH HHS P50 NS038377NINDS NIH HHS R01 NS112303NINDS NIH HHS R01 NS119280
6 · The paper itself

Abstract

Tau aggregation is a defining histopathological feature of Alzheimer's disease and other tauopathies. However, the cellular mechanisms involved in tau propagation remain unclear. Here, we performed an unbiased quantitative proteomic study to identify proteins that specifically interact with this tau seed. We identified Bassoon (BSN), a presynaptic scaffolding protein, as an interactor of the tau seed isolated from a mouse model of tauopathy, and from Alzheimer's disease and progressive supranuclear palsy postmortem samples. We show that BSN exacerbates tau seeding and toxicity in both mouse and Drosophila models for tauopathy, and that BSN downregulation decreases tau spreading and overall disease pathology, rescuing synaptic and behavioral impairments and reducing brain atrophy. Our findings improve the understanding of how tau seeds can be stabilized by interactors such as BSN. Inhibiting tau-seed interactions is a potential new therapeutic approach for neurodegenerative tauopathies.

Indexed as

Alzheimer DiseaseTauopathiesAnimalsBrainMiceProteomicstau Proteinstau Proteins

Identifiers

PMID36344699
PMCPMC9708566
OpenAlexW4308469604

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.