Evidence map›Paper›PMID 41750318›Full record

ArticleBiomolecules2026

Impaired TGFβ Signaling in Plaque-Associated Microglia.

Oliver Krzyzan, Angela Kuhla, Björn Spittau, Natascha Vidovic

Abstract read
In one paragraph

Article in Biomolecules, 2026. 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.

No citing paper in PubMed yet.

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

4 authors.

Oliver KrzyzanInstitute of Anatomy, Rostock Medical Centre, Rostock University, 18057 Rostock, Germany.
Angela KuhlaRudolf-Zenker Institute of Experimental Surgery, Rostock Medical Centre, Rostock University, 18057 Rostock, Germany.ORCID 0000-0002-7618-7663
Björn SpittauBielefeld University, Medical School OWL, Anatomy and Cell Biology, 33615 Bielefeld, Germany.ORCID 0000-0001-5423-0571
Natascha VidovicBielefeld University, Medical School OWL, Anatomy and Cell Biology, 33615 Bielefeld, Germany.ORCID 0000-0002-1426-7625

Funding

Deutsche Forschungsgemeinschaft SP 1555/2-3
6 · The paper itself

Abstract

Aging and Alzheimer's disease (AD) are associated with profound changes in glial cell morphology and signaling. This study investigates the three-dimensional morphology of microglia and the intracellular localization of phosphorylated SMAD proteins as downstream effectors of transforming growth factor β (TGF-β) signaling in the amyloid precursor protein and presenilin-1 (APP/PS1) transgenic mouse model of Alzheimer's disease. Using confocal microscopy and Simple Neurite Tracer software, we reconstructed and quantitatively analyzed glial cell morphology in aged wild-type and APP/PS1 mice. Immunofluorescence staining revealed altered pSMAD2 distribution in microglia, suggesting impaired canonical TGF-β signaling. Our findings indicate a disturbed glial morphology and dysfunctional TGF-β signaling cascade in the APP/PS1 model, underlining their potential role in Alzheimer's disease pathogenesis.

Indexed as

Alzheimer DiseaseMicrogliaPlaque, AmyloidSignal TransductionTransforming Growth Factor betaAmyloid beta-Protein PrecursorAnimalsDisease Models, AnimalHumansMiceMice, TransgenicPhosphorylationPresenilin-1Smad2 ProteinAmyloid beta-Protein PrecursorPresenilin-1Smad2 ProteinTransforming Growth Factor beta3D morphologyAlzheimer’s diseaseAPP/PS1confocal microscopymicroglianeuroinflammationSMAD proteinsTGF-β

Identifiers

PMID41750318
PMCPMC12937944

What Socratic 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 Socratic graph.