Evidence map›Paper›PMID 21515785›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

An endogenously anti-inflammatory role for methylation in mucosal inflammation identified through metabolite profiling.

Douglas J Kominsky, Simon Keely, Christopher F MacManus, Louise E Glover, Melanie Scully, Colm B Collins, Brittelle E Bowers, Eric L Campbell, Sean P Colgan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. MAT2A inhibition suppresses inflammation inJournal of oral microbiology · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Observational
  8. Article
  9. Hypoxia-inducible factor-dependent induction of myeloid-derived netrin-1 attenuates natural killer cell infiltration during endotoxin-induced lung injury.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. G2A Signaling Dampens Colitic Inflammation via Production of IFN-γ.Journal of immunology (Baltimore, Md. : 1950) · 2016
    Article
  19. Article
  20. lnflammation-induced epigenetic switches in cancer.Cellular and molecular life sciences : CMLS · 2016
    Review
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

9 authors at 2 institutions in 1 country.

Douglas J KominskyDepartment of Anesthesiology and Perioperative Medicine, University of Colorado Health Science Center, Aurora, CO 80045, USA. Douglas.Kominsky@ucdenver.edu
Simon Keely
Christopher F MacManus
Louise E Glover
Melanie Scully
Colm B Collins
Brittelle E Bowers
Eric L Campbell
Sean P Colgan
University of Colorado Denver · USUniversity of Colorado Hospital · US

Funding

Hypoxia, HIF, and Mucosal InflammationR37DK050189 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI COLGAN, SEAN P · 2010 to 2019
$4.1M
Neutrophils and Vascular Endothelial PermeabilityR01HL060569 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI COLGAN, SEAN P · 1999 to 2013
$3.5M
Inflammation-dependent methylation in the mucosaR01DK099452 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI KOMINSKY, DOUGLAS J · 2014 to 2017
$1.3M
NHLBI NIH HHS R01 HL060569NIDDK NIH HHS R01 DK099452NIDDK NIH HHS R37 DK050189
6 · The paper itself

Abstract

Tissues of the mucosa are lined by an epithelium that provides barrier and transport functions. It is now appreciated that inflammatory responses in inflammatory bowel diseases are accompanied by striking shifts in tissue metabolism. In this paper, we examined global metabolic consequences of mucosal inflammation using both in vitro and in vivo models of disease. Initial analysis of the metabolic signature elicited by inflammation in epithelial models and in colonic tissue isolated from murine colitis demonstrated that levels of specific metabolites associated with cellular methylation reactions are significantly altered by model inflammatory systems. Furthermore, expression of enzymes central to all cellular methylation, S-adenosylmethionine synthetase and S-adenosylhomocysteine hydrolase, are increased in response to inflammation. Subsequent studies showed that DNA methylation is substantially increased during inflammation and that epithelial NF-κB activity is significantly inhibited following treatment with a reversible S-adenosylhomocysteine hydrolase inhibitor, DZ2002. Finally, these studies demonstrated that inhibition of cellular methylation in a murine model of colitis results in disease exacerbation while folate supplementation to promote methylation partially ameliorates the severity of murine colitis. Taken together, these results identify a global change in methylation, which during inflammation, translates to an overall protective role in mucosal epithelia.

Indexed as

AdenineAdenosylhomocysteinaseAnimalsBlotting, WesternButyratesCell Line, TumorColitisColonDextran SulfateDNA MethylationEpithelial CellsGene Expression ProfilingHeLa CellsHumansInflammationInterferon-gammaAdenineAdenosylhomocysteinaseButyratesDextran SulfateInterferon-gammaMethionine Adenosyltransferasemethyl 4-(adenin-9-yl)-2-hydroxybutanoateNF-kappa B

Identifiers

PMID21515785
PMCPMC3383860
OpenAlexW2155563269

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.