Evidence map›Paper›PMID 21703412›Full record

ArticleThe American journal of pathology2011

Dual functions of prostaglandin D2 in murine contact hypersensitivity via DP and CRTH2.

Yoshihiro Yamamoto, Shinobu Otani, Hiroyuki Hirai, Kinya Nagata, Kosuke Aritake, Yoshihiro Urade, Shuh Narumiya, Hiroo Yokozeki, Masataka Nakamura, Takahiro Satoh

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 31 citations in OpenAlex.

  1. Regulatory Roles of Phospholipase AFrontiers in immunology · 2022
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Prostaglandin D2 receptor D-type prostanoid receptor 2 mediates eosinophil trafficking into the esophagus.Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus · 2014
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Yoshihiro YamamotoDepartment of Dermatology, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan.
Shinobu Otani
Hiroyuki Hirai
Kinya Nagata
Kosuke Aritake
Yoshihiro Urade
Shuh Narumiya
Hiroo Yokozeki
Masataka Nakamura
Takahiro Satoh
Tokyo Medical and Dental University · JPMedical & Biological Laboratories (Japan) · JPOsaka Science Museum · JPKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostaglandin D2 (PGD2) exerts its effects through two distinct receptors: the chemoattractant receptor-homologous molecule expressed on Th2 cells (CRTH2) and the D prostanoid (DP) receptor. Our previous study demonstrated that CRTH2 mediates contact hypersensitivity (CHS) in mice. However, the function of DP receptor remains to be fully established. In this study, we examine the pathophysiological roles of PGD2 using DP-deficient (DP(-/-)) and CRTH2/DP-deficient (CRTH2(-/-)/DP(-/-)) mice to elucidate receptor-mediated PGD2 action in CHS. We observed profound exacerbation of CHS in DP(-/-) mice. CRTH2(-/-)/DP(-/-) mice showed similar exacerbation, but to a lesser extent. These symptoms were accompanied by increased production of interferon-γ and IL-17. The increase in IL-17 producing γδ T cells was marked and presumably contributed to the enhanced CHS. DP deficiency promoted the in vivo migration of dendritic cells to regional lymph nodes. A DP agonist added to DCs in vitro was able to inhibit production of IL-12 and IL-1β. Interestingly, production of IL-10 in dendritic cells was elevated via the DP pathway, but it was lowered by the CRTH2 pathway. Collectively, PGD2 signals through CRTH2 to mediate CHS inflammation, and conversely, DP signals to exert inhibitory effects on CHS. Thus, we report opposing functions for PGD2 that depend on receptor usage in allergic reactions.

Indexed as

AnimalsBlotting, WesternCell MovementChemokinesCytokinesDermatitis, ContactFemaleFlow CytometryGene Rearrangement, delta-Chain T-Cell Antigen ReceptorGene Rearrangement, gamma-Chain T-Cell Antigen ReceptorInflammationInterleukin-10Interleukin-12Interleukin-17Interleukin-1betaMaleChemokinesCytokinesInterleukin-10Interleukin-12Interleukin-17Interleukin-1betaProstaglandin D2prostaglandin D2 receptorprostanoid D receptor 1, mouseReceptors, ImmunologicReceptors, ProstaglandinRNA, Messenger

Identifiers

PMID21703412
PMCPMC3123801
OpenAlexW2145957843

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.