Evidence map›Paper›PMID 42004171›Full record

ArticleBlood vessels, thrombosis & hemostasis2026

Murine thrombus organization limits access to high platelet activation states while supporting platelet recruitment.

Sung W Rhee, Irina D Pokrovskaya, Kelly K Ball, Michael W Webb, Jeffrey A Kamykowski, Maria A Aronova, Richard D Leapman, Elizabeth R Driehaus, Erich S Franz, Sidney W Whiteheart and 1 more

Abstract read
In one paragraph

Article in Blood vessels, thrombosis & hemostasis, 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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0citing papers in PubMed
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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

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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

11 authors.

Sung W RheeDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR.
Irina D PokrovskayaDepartment of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR.
Kelly K BallDepartment of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR.
Michael W WebbDepartment of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR.
Jeffrey A KamykowskiDepartment of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR.
Maria A AronovaLaboratory of Cellular Imaging and Macromolecular Biophysics, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD.
Richard D LeapmanLaboratory of Cellular Imaging and Macromolecular Biophysics, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD.
Elizabeth R DriehausDepartment of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, KY.
Erich S FranzDepartment of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, KY.
Sidney W WhiteheartDepartment of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, KY.
Brian StorrieDepartment of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platelet aggregation at sites of vascular injury is essential for hemostasis. However, the mechanisms that prevent excessive clot growth are not fully understood. In the prevailing "core and shell" model, based largely on small vessel injury studies, a central core of highly activated platelets is surrounded by a limited signal intensity shell of less activated, minimally degranulated platelets. Recent reports, especially in mouse models of profuse bleeding, suggest thrombus architecture and platelet activation states are more heterogeneous than the binary core and shell model proposes. Here, we performed high-resolution morphometric mapping of individual platelet activation states in mouse jugular vein and femoral artery puncture wound thrombi, using serial block face scanning electron microscopy and wide-area transmission electron microscopy. Manually annotated images were analyzed at multiple time points, revealing initial, 1-minute, near-complete intermixing of platelet activation states with no distinct core of highly activated platelets. At 5 minutes, highly activated, degranulated platelets became concentrated along the interior surfaces of vaulted thrombus structures. At 20 minutes, platelet numbers decreased and distinct clustering of degranulated, highly activated platelets was observed within central portions of the intravascular platelet-rich crown, limiting their access to the circulation. Deletion of the α-granule vesicle-soluble N-ethylmaleimide-sensitive factor attachment protein receptor, vesicle associated membrane protein 8, increased both the frequency and clustering of highly activated platelets. Similar patterns were observed in femoral artery wounds. We conclude that thrombus organization is more complex than previously recognized and provide evidence that progressive structural changes help limit procoagulant surface exposure and thrombus growth during hemostasis after puncture wounding.

Identifiers

PMID42004171
PMCPMC13091196

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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.