Evidence map›Paper›PMID 18270204›Full record

ArticleThe Journal of biological chemistry2008

Prostaglandin E receptor type 4-associated protein interacts directly with NF-kappaB1 and attenuates macrophage activation.

Manabu Minami, Koichi Shimizu, Yoshihisa Okamoto, Eduardo Folco, Marco-Lopez Ilasaca, Mark W Feinberg, Masanori Aikawa, Peter Libby

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
7.7field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. The Link between Prostanoids and Cardiovascular Diseases.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Article
  8. Multiple genome viewer (MGV): a new tool for visualization and comparison of multiple annotated genomes.Mammalian genome : official journal of the International Mammalian Genome Society · 2022
    Article
  9. Article
  10. Review
  11. Immune-enhancing effects of gamma-irradiated sericin.Food science and biotechnology · 2020
    Article
  12. Article
  13. Article
  14. Prostaglandin EProstaglandins & other lipid mediators · 2019
    Article
  15. Review
  16. Article
  17. Article
  18. Prostaglandin E receptor-4 receptor mediates endothelial barrier-enhancing and anti-inflammatory effects of oxidized phospholipids.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  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

8 authors at 2 institutions in 1 country.

Manabu MinamiCardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.
Koichi Shimizu
Yoshihisa Okamoto
Eduardo Folco
Marco-Lopez Ilasaca
Mark W Feinberg
Masanori Aikawa
Peter Libby
Brigham and Women's Hospital · USHarvard University · US

Funding

Inflammatory Mechanisms of AtherosclerosisR01HL034636 · NHLBI · TUFTS UNIVERSITY BOSTON · PI LIBBY, PETER · 1985 to 2006
$1.9M
CONTROL OF GROWTH OF VASCULAR WALL CELLSR37HL034636 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LIBBY, PETER · 1993 to 2002
$1.2M
NHLBI NIH HHS HL 34636
6 · The paper itself

Abstract

Macrophage activation participates pivotally in the pathophysiology of chronic inflammatory diseases, including atherosclerosis. Through the receptor EP4, prostaglandin E(2) (PGE(2)) exerts an anti-inflammatory action in macrophages, suppressing stimulus-induced expression of certain proinflammatory genes, including chemokines. We recently identified a novel EP4 receptor-associated protein (EPRAP), whose function in PGE(2)-mediated anti-inflammation remains undefined. Here we demonstrate that PGE(2) pretreatment selectively inhibits lipopolysaccharide (LPS)-induced nuclear factor kappaB1 (NF-kappaB1) p105 phosphorylation and degradation in mouse bone marrow-derived macrophages through EP4-dependent mechanisms. Similarly, directed EPRAP expression in RAW264.7 cells suppresses LPS-induced p105 phosphorylation and degradation, and subsequent activation of mitogen-activated protein kinase kinase 1/2. Forced expression of EPRAP also inhibits NF-kappaB activation induced by various proinflammatory stimuli in a concentration-dependent manner. In co-transfected cells, EPRAP, which contains multiple ankyrin repeat motifs, directly interacts with NF-kappaB1 p105/p50 and forms a complex with EP4. In EP4-overexpressing cells, PGE(2) enhances the protective action of EPRAP against stimulus-induced p105 phosphorylation, whereas EPRAP silencing in RAW264.7 cells impairs the inhibitory effect of PGE(2)-EP4 signaling on LPS-induced p105 phosphorylation. Additionally, EPRAP knockdown as well as deficiency of NF-kappaB1 in macrophages attenuates the inhibitory effect of PGE(2) on LPS-induced MIP-1beta production. Thus, PGE(2)-EP4 signaling augments NF-kappaB1 p105 protein stability through EPRAP after proinflammatory stimulation, limiting macrophage activation.

Indexed as

Macrophage ActivationAmino Acid MotifsAnimalsAtherosclerosisBone Marrow CellsCell Cycle ProteinsCell LineChemokinesDinoprostoneGene SilencingHumansLipopolysaccharidesMacrophagesMAP Kinase Kinase 1MAP Kinase Kinase 2MiceCell Cycle ProteinsChemokinesDinoprostoneFEM1A protein, humanFem1a protein, mouseLipopolysaccharidesMAP2K1 protein, humanMap2k1 protein, mouseMAP2K2 protein, humanMap2k2 protein, mouseMAP Kinase Kinase 1MAP Kinase Kinase 2NF-kappa B p50 SubunitPTGER4 protein, humanPtger4 protein, mouseReceptors, Prostaglandin EReceptors, Prostaglandin E, EP4 Subtype

Identifiers

PMID18270204
PMCPMC2442287
OpenAlexW1971442486

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.