Evidence mapPaperPMID 41495365Full record

ArticleCellular and molecular neurobiology2026

Procoagulant Extracellular Vesicles Increase Neuronal Tau expression, Metabolism and Processing Through Tissue Factor and Protease Activated Receptor 2.

Sophie J Featherby, Eamon C Faulkner, Andrew Gordon, Camille Ettelaie

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Article in Cellular and molecular neurobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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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.

Sophie J Featherby *Centre for Biomedicine, Hull-York Medical School, Cottingham Road, Hull, HU6 7RX, UK.ORCID http://orcid.org/0000-0003-0982-7349
Eamon C FaulknerCentre for Biomedicine, Hull-York Medical School, Cottingham Road, Hull, HU6 7RX, UK.ORCID http://orcid.org/0000-0002-2628-6049
Andrew GordonCentre for Biomedicine, Hull-York Medical School, Cottingham Road, Hull, HU6 7RX, UK.ORCID http://orcid.org/0000-0003-2770-6129
Camille Ettelaie *Centre for Biomedicine, Hull-York Medical School, Cottingham Road, Hull, HU6 7RX, UK. C.Ettelaie@hull.ac.uk.ORCID http://orcid.org/0000-0002-6121-5262

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuro-inflammation is implicated in the onset of neuropathologies and can be promoted by stroke, trauma, toxins or infections. Brain tissue is rich in Tissue factor (TF) which is also released within cerebrospinal fluid as extracellular vesicles (EV). TF is an inflammatory protein which is increased during chronic conditions, and initiates blood coagulation and promotes tissue repair. This study examined the influence of TF on the expression, phosphorylation, aggregation and degradation of Tau protein in differentiated human cells SH-SY5Y and HCN-2, and rat neuronal cells. Studies were performed using vesicles containing TF or recombinant TF supplemented with factor VIIa (fVIIa) and also in the presence of various reagents and antibodies. Treatment of the differentiated cells with TF or TF-EV, upregulated the expression of Tau mRNA and protein, and was enhanced on repeated treatment. Incubation of cells with TF-fVIIa increased Tau expression and resulted in significant phosphorylation at Thr181, and was less at Ser202. Inhibition of the protease activity of TF-fVIIa, or blocking PAR2 activation on cells using SAM11 antibody, reduced Tau phosphorylation at Thr181. Examination of the Tau protein at intervals post-treatment indicated that Thr181 phosphorylation was present in bands of approximately 50 and 30-35 kDa while phosphorylation of Ser202 was associated with a 43 kDa band. Exposure of the cells to TF alone was sufficient to induce PKC-dependent phosphorylation of Tau. Prolonged treatment of differentiated SH-SY5Y cells with TF, resulted in higher staining with Amytracker dye. Finally, controlled digestion of recombinant full-length Tau with TF-fVIIa resulted in a smaller fragment. In conclusion, our data presents potential mechanisms by which TF influences Tau metabolism in neurons, being both beneficial in terms of clearance and regeneration, and having detrimental outcomes including aggregation.

Indexed as

CoagulantsExtracellular VesiclesNeuronsReceptor, PAR-2tau ProteinsThromboplastinAnimalsCell Line, TumorFactor VIIaHumansPhosphorylationRatsCoagulantsFactor VIIaReceptor, PAR-2tau ProteinsThromboplastinAggregationExtracellular vesiclesFactor VIIaNeuronal cellsNeuropathiesPhosphorylationProtease activated receptor 2Proteolytic digestionTauTissue factor

Identifiers

PMID41495365
PMCPMC12847580

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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 Socratic graph.