Evidence map›Paper›PMID 19073150›Full record

ArticleBiochemical pharmacology2009

RhoA downstream of G(q) and G(12/13) pathways regulates protease-activated receptor-mediated dense granule release in platelets.

Jianguo Jin, Yingying Mao, Dafydd Thomas, Soochong Kim, James L Daniel, Satya P Kunapuli

Open access · greenAbstract read
In one paragraph

Article in Biochemical pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Arhgef1 Plays a Vital Role in Platelet Function and Thrombogenesis.Journal of the American Heart Association · 2019
    Article
  13. Article
  14. The functional role of protease-activated receptors on contractile responses by activation of CaAmerican journal of physiology. Gastrointestinal and liver physiology · 2018
    Article
  15. Article
  16. Article
  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

6 authors at 1 institution in 1 country.

Jianguo JinDepartment of Physiology, Temple University School of Medicine, Philadelphia, PA, USA.
Yingying Mao
Dafydd Thomas
Soochong Kim
James L Daniel
Satya P Kunapuli
Temple University · US

Funding

MOLECULAR BASIS FOR ADP INDUCED PLATELET ACTIVATIONR01HL060683 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KUNAPULI, SATYA P. · 1998 to 2011
$3.9M
Functional PKC Isoforms in PlateletsR01HL093231 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KUNAPULI, SATYA P. · 2009 to 2017
$3.6M
Functional G Protein pathways in platelet activationR01HL081322 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KUNAPULI, SATYA P. · 2006 to 2010
$2.9M
Platelet ADP ReceptorsR01HL080444 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KUNAPULI, SATYA P. · 2005 to 2008
$1.8M
NHLBI NIH HHS HL60683NHLBI NIH HHS HL80444NHLBI NIH HHS HL81322NHLBI NIH HHS R01 HL060683NHLBI NIH HHS R01 HL080444NHLBI NIH HHS R01 HL081322NHLBI NIH HHS R01 HL093231
6 · The paper itself

Abstract

Platelet secretion is an important physiological event in hemostasis. The protease-activated receptors, PAR 1 and PAR 4, and the thromboxane receptor activate the G(12/13) pathways, in addition to the G(q) pathways. Here, we investigated the contribution of G(12/13) pathways to platelet dense granule release. 2MeSADP, which does not activate G(12/13) pathways, does not cause dense granule release in aspirin-treated platelets. However, supplementing 2MeSADP with YFLLRNP (60muM), as selective activator of G(12/13) pathways, resulted in dense granule release. Similarly, supplementing PLC activation with G(12/13) stimulation also leads to dense granule release. These results demonstrate that supplemental signaling from G(12/13) is required for G(q)-mediated dense granule release and that ADP fails to cause dense granule release because the platelet P2Y receptors, although activate PLC, do not activate G(12/13) pathways. When RhoA, downstream signaling molecule in G(12/13) pathways, is blocked, PAR-mediated dense granule release is inhibited. Furthermore, ADP activated RhoA downstream of G(q) and upstream of PLC. Finally, RhoA regulated PKCdelta T505 phosphorylation, suggesting that RhoA pathways contribute to platelet secretion through PKCdelta activation. We conclude that G(12/13) pathways, through RhoA, regulate dense granule release and fibrinogen receptor activation in platelets.

Indexed as

Adenosine DiphosphateAspirinBlood PlateletsBlotting, WesternCytoplasmic GranulesEnzyme ActivationGTP-Binding ProteinsHumansIn Vitro TechniquesOligopeptidesPeptides, CyclicProtein Kinase C-deltaReceptor, PAR-1Receptors, ThrombinrhoA GTP-Binding ProteinThionucleotidesAdenosine Diphosphatealanyl-tyrosyl-prolyl-glycyl-lysyl-phenylalanineAspirinGTP-Binding Proteinsmethylthio-ADPOligopeptidesPeptides, Cyclicprotease-activated receptor 4Protein Kinase C-deltaReceptor, PAR-1Receptors, ThrombinrhoA GTP-Binding ProteinThionucleotidesType C Phospholipasestyrosyl-phenylalanyl-leucyl-leucyl-arginyl-asparaginyl-arginineYM-254890

Identifiers

PMID19073150
PMCPMC2745276
OpenAlexW1968817307

What OpenQuestion holds

Textmetadata
LicenceTDM
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.