Evidence map›Paper›PMID 35034417›Full record

ArticleJournal of thrombosis and haemostasis : JTH2022

Maintaining flippase activity in procoagulant platelets is a novel approach to reducing thrombin generation.

Sarah L Millington-Burgess, Matthew T Harper

Open access · hybridAbstract read
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
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

11 citing papers in PubMed, 15 citations in OpenAlex.

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  9. Procoagulant platelets: novel players in thromboinflammation.American journal of physiology. Cell physiology · 2022
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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

2 authors at 1 institution in 1 country.

Sarah L Millington-BurgessDepartment of Pharmacology, University of Cambridge, Cambridge, UK.ORCID 0000-0001-6549-920X
Matthew T HarperDepartment of Pharmacology, University of Cambridge, Cambridge, UK.ORCID 0000-0002-4740-637X
University of Cambridge · GB

Funding

British Heart Foundation FS/15/62/32032British Heart Foundation PG/20/12/34982
6 · The paper itself

Abstract

backgroundDuring thrombosis, procoagulant platelets expose phosphatidylserine (PS), which enhances local thrombin generation. Reducing platelet PS exposure could be a novel anti-thrombotic approach. PS is confined to the inner leaflet of the plasma membrane in unstimulated platelets by ATP-dependent "flippase" activity. Ca

objectivesTo determine the mechanism by which R5421 reduces platelet PS exposure.

methodsWashed human platelets were stimulated with the Ca RESULTS AND

conclusionsR5421 reduced the extent of A23187-stimulated platelet PS exposure, as demonstrated with annexin V or lactadherin binding. R5421 also maintained flippase activity in procoagulant platelets. Although R5421 appeared to inhibit scramblase activity in procoagulant platelets, it did not once the flippase had been inhibited, demonstrating that scramblase activity is not directly inhibited. Furthermore, R5421 inhibited the contribution of A23187-stimulated platelets to thrombin generation. Together these data demonstrate that R5421 reduces the extent of PS exposure in procoagulant platelets by maintaining flippase activity. Maintaining flippase activity in procoagulant platelets is a novel and effective approach to reducing thrombin generation.

Indexed as

ThrombinThrombosisAnnexin A5Blood PlateletsCalcimycinHumansIonophoresPhosphatidylserinesAnnexin A5CalcimycinIonophoresPhosphatidylserinesThrombinblood plateletspharmacologyphosphatidylserinephospholipid transfer proteinsthrombosis

Identifiers

PMID35034417
PMCPMC9306496
OpenAlexW4205397620

What OpenQuestion 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 OpenQuestion graph.