Evidence map›Paper›PMID 25404741›Full record

ArticleThe Journal of biological chemistry2015

Syntaxin 8 regulates platelet dense granule secretion, aggregation, and thrombus stability.

Ewelina M Golebiewska, Matthew T Harper, Christopher M Williams, Joshua S Savage, Robert Goggs, Gabriele Fischer von Mollard, Alastair W Poole

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Platelet-Derived Extracellular Vesicles in Arterial Thrombosis.Advances in experimental medicine and biology · 2023
    Article
  8. Identification ofPathogens (Basel, Switzerland) · 2021
    Article
  9. Article
  10. Platelet δ-Storage Pool Disease: An Update.Journal of clinical medicine · 2020
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article
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

7 authors at 2 institutions in 1 country.

Ewelina M GolebiewskaFrom the School of Physiology and Pharmacology, Medical Sciences Building, University Walk, Bristol BS8 1TD, United Kingdom.
Matthew T HarperFrom the School of Physiology and Pharmacology, Medical Sciences Building, University Walk, Bristol BS8 1TD, United Kingdom.
Christopher M WilliamsFrom the School of Physiology and Pharmacology, Medical Sciences Building, University Walk, Bristol BS8 1TD, United Kingdom.
Joshua S Savagethe School of Cancer Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom.
Robert Goggsthe Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York 14853, and.
Gabriele Fischer von Mollardthe Fakultät für Chemie, Biochemie III, Universität Bielefeld, Postfach 100131, 33501 Bielefeld, Germany.
Alastair W PooleFrom the School of Physiology and Pharmacology, Medical Sciences Building, University Walk, Bristol BS8 1TD, United Kingdom, a.poole@bris.ac.uk.
University of Bristol · GBUniversity of Birmingham · GB

Funding

British Heart Foundation FS/09/009/26444British Heart Foundation PG/12/25/29488British Heart Foundation RG/10/006/28299
6 · The paper itself

Abstract

Platelet secretion not only drives thrombosis and hemostasis, but also mediates a variety of other physiological and pathological processes. The ubiquitous SNARE machinery and a number of accessory proteins have been implicated in regulating secretion in platelet. Although several platelet SNAREs have been identified, further members of the SNARE family may be needed to fine-tune platelet secretion. In this study we identified expression of the t-SNARE syntaxin 8 (STX8) (Qc SNARE) in mouse and human platelets. In mouse studies, whereas STX8 was not essential for α-granule or lysosome secretion, Stx8(-/-) platelets showed a significant defect in dense granule secretion in response to thrombin and CRP. This was most pronounced at intermediate concentrations of agonists. They also showed an aggregation defect that could be rescued with exogenous ADP and increased embolization in Stx8(-/-) mice in vivo consistent with an important autocrine and paracrine role for ADP in aggregation and thrombus stabilization. STX8 therefore specifically contributes to dense granule secretion and represents another member of a growing family of genes that play distinct roles in regulating granule release from platelets and thus platelet function in thrombosis and hemostasis.

Indexed as

Adenosine DiphosphateAdenosine TriphosphateAnimalsBlood PlateletsDigitoninExocytosisFlow CytometryHemostasisHumansLysosomesMiceMice, Inbred C57BLMice, TransgenicPlatelet ActivationQa-SNARE ProteinsSecretory VesiclesAdenosine DiphosphateAdenosine TriphosphateDigitoninQa-SNARE ProteinsSNARE ProteinsADPExocytosisPlateletSNARE ProteinsThrombosis

Identifiers

PMID25404741
PMCPMC4340400
OpenAlexW2036729274

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.