Evidence map›Paper›PMID 18077391›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Hematopoietic prostaglandin D2 synthase controls the onset and resolution of acute inflammation through PGD2 and 15-deoxyDelta12 14 PGJ2.

Ravindra Rajakariar, Mark Hilliard, Toby Lawrence, Seema Trivedi, Paul Colville-Nash, Geoff Bellingan, Desmond Fitzgerald, Muhammad M Yaqoob, Derek W Gilroy

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers.

0numbers the graph read from it
0cells of the map it votes in
127citing papers in PubMed
13.7field-weighted citation impact, top 1% 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

127 citing papers in PubMed, 251 citations in OpenAlex.

  1. Trial
  2. Niacin and biosynthesis of PGD₂by platelet COX-1 in mice and humans.The Journal of clinical investigation · 2012 · on this map
    Trial
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
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  10. Article
  11. Article
  12. Article
  13. The Link between Prostanoids and Cardiovascular Diseases.International journal of molecular sciences · 2023
    Review
  14. Review
  15. Biosynthesis of prostaglandin 15dPGJJournal of lipid research · 2022
    Article
  16. Review
  17. MicroRNAs in shaping the resolution phase of inflammation.Seminars in cell & developmental biology · 2022
    Review
  18. Article
  19. Article
  20. Review

67 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 2 countries.

Ravindra RajakariarDepartment of Experimental Medicine, Nephrology, and Critical Care, William Harvey Research Institute, Charterhouse Square, London EC1M 6BQ, United Kingdom.
Mark Hilliard
Toby Lawrence
Seema Trivedi
Paul Colville-Nash
Geoff Bellingan
Desmond Fitzgerald
Muhammad M Yaqoob
Derek W Gilroy
University College Dublin · IEUniversity College London · GBWilliam Harvey Research Institute · GBImperial College London · GBSt Helier Hospital · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Hematopoietic prostaglandin D(2) synthase (hPGD(2)S) metabolizes cyclooxygenase (COX)-derived PGH(2) to PGD(2) and 15-deoxyDelta(12-14) PGJ(2) (15d-PGJ(2)). Unlike COX, the role of hPGD(2)S in host defense is ambiguous. PGD(2) can be either pro- or antiinflammatory depending on disease etiology, whereas the existence of 15d-PGJ(2) and its relevance to pathophysiology remain controversial. Herein, studies on hPGD(2)S KO mice reveal that 15d-PGJ(2) is synthesized in a self-resolving peritonitis, detected by using liquid chromatography-tandem MS. Together with PGD(2) working on its DP1 receptor, 15d-PGJ(2) controls the balance of pro- vs. antiinflammatory cytokines that regulate leukocyte influx and monocyte-derived macrophage efflux from the inflamed peritoneal cavity to draining lymph nodes leading to resolution. Specifically, inflammation in hPGD(2)S KOs is more severe during the onset phase arising from a substantial cytokine imbalance resulting in enhanced polymorphonuclear leukocyte and monocyte trafficking. Moreover, resolution is impaired, characterized by macrophage and surprisingly lymphocyte accumulation. Data from this work place hPGD(2)S at the center of controlling the onset and the resolution of acute inflammation where it acts as a crucial checkpoint controller of cytokine/chemokine synthesis as well as leukocyte influx and efflux. Here, we provide definitive proof that 15d-PGJ(2) is synthesized during mammalian inflammatory responses, and we highlight DP1 receptor activation as a potential antiinflammatory strategy.

Indexed as

InflammationAcute DiseaseAnimalsAnti-Inflammatory AgentsDrug DesignEicosanoidsHematopoietic Stem CellsImmunity, InnateIntramolecular OxidoreductasesLeukocytesLipocalinsMiceMice, KnockoutMonocytesNeutrophilsProstaglandin D215-deoxy-delta(12,14)-prostaglandin J2Anti-Inflammatory AgentsEicosanoidsIntramolecular OxidoreductasesLipocalinsProstaglandin D2Prostaglandin-Endoperoxide Synthasesprostaglandin R2 D-isomerase

Identifiers

PMID18077391
PMCPMC2409252
OpenAlexW2162311264

What OpenQuestion holds

Textmetadata
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.