Evidence map›Paper›PMID 26828924›Full record

ArticlePloS one2016

OGR1/GPR68 Modulates the Severity of Experimental Autoimmune Encephalomyelitis and Regulates Nitric Oxide Production by Macrophages.

Cheryl A D'Souza, Fei Linda Zhao, Xujian Li, Yan Xu, Shannon E Dunn, Li Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Physiological relevance of proton-activated GPCRs.Pflugers Archiv : European journal of physiology · 2022
    Review
  7. The Roles of Orphan G Protein-Coupled Receptors in Autoimmune Diseases.Clinical reviews in allergy & immunology · 2021
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. 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 3 institutions in 2 countries.

Cheryl A D'SouzaToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Fei Linda ZhaoDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Xujian LiToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Yan XuDepartment of Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.
Shannon E DunnToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
Li ZhangToronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
University Health Network · CAUniversity of Toronto · CAIndiana University – Purdue University Indianapolis · US

Funding

Role of immune cell OGR1 in prostate cancer development and the mechanisms involvR01CA155145 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI XU, YAN, ZHANG, LI · 2011 to 2015
$2.0M
CIHR MOP341319NCI NIH HHS 5R01CA155145NCI NIH HHS R01 CA155145
6 · The paper itself

Abstract

Ovarian cancer G protein-coupled receptor 1 (OGR1) is a proton-sensing molecule that can detect decreases in extracellular pH that occur during inflammation. Although OGR1 has been shown to have pro-inflammatory functions in various diseases, its role in autoimmunity has not been examined. We therefore sought to determine whether OGR1 has a role in the development of T cell autoimmunity by contrasting the development of experimental autoimmune encephalomyelitis between wild type and OGR1-knockout mice. OGR1-knockout mice showed a drastically attenuated clinical course of disease that was associated with a profound reduction in the expansion of myelin oligodendrocyte glycoprotein 35-55-reactive T helper 1 (Th1) and Th17 cells in the periphery and a reduced accumulation of Th1 and Th17 effectors in the central nervous system. We determined that these impaired T cell responses in OGR1-knockout mice associated with a reduced frequency and number of dendritic cells in draining lymph nodes during EAE and a higher production of nitric oxide by macrophages. Our studies suggest that OGR1 plays a key role in regulating T cell responses during autoimmunity.

Indexed as

AnimalsAntigen-Presenting CellsAntigensCell DifferentiationCell ProliferationCell SurvivalCytokinesEncephalomyelitis, Autoimmune, ExperimentalEpitopesFemaleLymphocyte CountMacrophagesMice, KnockoutNitric OxideReceptors, G-Protein-CoupledTh17 CellsAntigensCytokinesEpitopesGPR68 protein, mouseNitric OxideReceptors, G-Protein-Coupled

Identifiers

PMID26828924
PMCPMC4735495
OpenAlexW2259397374

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.