Evidence map›Paper›PMID 40654124›Full record

ReviewCurrent opinion in hematology2025

Humanized murine models of platelet function.

Javier Menéndez-Pérez, Abigail Ajanel, Robert A Campbell

Abstract readReview
In one paragraph

Review in Current opinion in hematology, 2025. 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

3 authors.

Javier Menéndez-PérezDepartment of Emergency Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Abigail Ajanel
Robert A Campbell

Funding

HUMAN PLATELET PAR4: NOVEL ACTIVATION, INTERINDIVIDUAL VARIATION, AND NEUTROPHIL INTERACTIONS IN VIVO AND IN VITROR01HL160808 · NHLBI · WASHINGTON UNIVERSITY · PI CAMPBELL, ROBERT A · 2022 to 2025
$2.1M
NHLBI NIH HHS R01 HL160808
6 · The paper itself

Abstract

purpose of reviewIn this review, we will describe murine models developed to examine human platelet function. RECENT

findingsPlatelets are critical cells necessary to regulate hemostasis after vessel injury. However, excessive platelet activation can lead to thrombotic complications. Preclinical/translational models are critical in developing therapeutics against platelet activation and to understand mechanistically how platelets function. Researchers have relied on murine models to study platelet function in vivo due to ease of establishing genetic knockouts as well as their lower cost and high throughput nature compared to larger animal models. However, while murine platelets are similar to human based on transcriptomic and proteomic analysis, there are significant differences between the two species, which limits their translation to the human system. To overcome these hurdles, investigators have targeted human platelet genes into the murine genome to express human receptors in mouse platelets. In addition, transfusion models of human platelets into mice have provided valuable insight into human platelet function. SUMMARY: Murine models are a value tool to examine platelet function in hemostasis and thrombosis. Continued focus on developing mouse models where platelets resemble those circulating in humans will offer valuable insight into important pathways, which may be targeted in the future.

Indexed as

Blood PlateletsAnimalsDisease Models, AnimalHemostasisHumansMicePlatelet ActivationThrombosishemostasismegakaryocytesmouse modelsplateletsthrombosis

Identifiers

PMID40654124
PMCPMC12262182

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Registered trials

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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.