Evidence map›Paper›PMID 37293074›Full record

ArticlebioRxiv : the preprint server for biology2023

Endogenous pathology in tauopathy mice progresses via brain networks.

Denise M O Ramirez, Jennifer D Whitesell, Nikhil Bhagwat, Talitha L Thomas, Apoorva D Ajay, Ariana Nawaby, Benoît Delatour, Sylvie Bay, Pierre LaFaye, Joseph E Knox and 3 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 10 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 3 countries.

Denise M O RamirezDepartment of Neurology, Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center; Dallas, TX, USA.
Jennifer D WhitesellAllen Institute for Brain Science; Seattle, WA, USA.
Nikhil BhagwatAllen Institute for Brain Science; Seattle, WA, USA.
Talitha L ThomasCenter for Alzheimer's and Neurodegenerative Diseases, Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center; Dallas, TX, USA.
Apoorva D AjayDepartment of Neurology, Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center; Dallas, TX, USA.
Ariana NawabyDepartment of Neurology, Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center; Dallas, TX, USA.
Benoît DelatourParis Brain Institute (ICM), CNRS UMR 7225, INSERM U1127, Sorbonne Université, Hôpital de la Pitié-Salpêtrière; Paris, France.
Sylvie BayUnité de Chimie des Biomolécules, Institut Pasteur, Université Paris Cité, CNRS UMR 3523; Paris, France.
Pierre LaFayeAntibody Engineering Platform, Institut Pasteur, Université Paris Cité, CNRS UMR 3528; Paris, France.
Joseph E KnoxAllen Institute for Brain Science; Seattle, WA, USA.
Julie A HarrisAllen Institute for Brain Science; Seattle, WA, USA.
Julian P MeeksDepartment of Neuroscience, University of Rochester Medical School; Rochester, NY, USA.
Marc I DiamondCenter for Alzheimer's and Neurodegenerative Diseases, Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center; Dallas, TX, USA.
The University of Texas Southwestern Medical Center · USAllen Institute for Brain Science · USCentre National de la Recherche Scientifique · FRMontreal Neurological Institute and Hospital · CAUniversity of Rochester · US

Funding

Identification and characterization of tau seeding and strain composition in tauopathyRF1AG059689 · NIA · UT SOUTHWESTERN MEDICAL CENTER · PI DIAMOND, MARC I, WHITE, CHARLES LEE · 2019 to 2019
$3.4M
Mouse Cell Type-Specific Brain Mapping in Health and DiseaseR01AG047589 · NIA · ALLEN INSTITUTE · PI HARRIS, JULIE · 2014 to 2018
$3.4M
Investigating information processing in parallel circuits that link external chemical signals to social behaviorR21NS104826 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI MEEKS, JULIAN P · 2017 to 2018
$421k
NIA NIH HHS R01 AG047589NIA NIH HHS RF1 AG059689NINDS NIH HHS R21 NS104826
6 · The paper itself

Abstract

Neurodegenerative tauopathies are hypothesized to propagate via brain networks. This is uncertain because we have lacked precise network resolution of pathology. We therefore developed whole-brain staining methods with anti-p-tau nanobodies and imaged in 3D PS19 tauopathy mice, which have pan-neuronal expression of full-length human tau containing the P301S mutation. We analyzed patterns of p-tau deposition across established brain networks at multiple ages, testing the relationship between structural connectivity and patterns of progressive pathology. We identified core regions with early tau deposition, and used network propagation modeling to determine the link between tau pathology and connectivity strength. We discovered a bias towards retrograde network-based propagation of tau. This novel approach establishes a fundamental role for brain networks in tau propagation, with implications for human disease.

Identifiers

PMID37293074
PMCPMC10245958
OpenAlexW4378228627

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.