Evidence map›Paper›PMID 21493784›Full record

ArticleAmerican journal of respiratory cell and molecular biology2011

Histone acetylation regulates the cell-specific and interferon-γ-inducible expression of extracellular superoxide dismutase in human pulmonary arteries.

Igor N Zelko, Marcus W Stepp, Alan L Vorst, Rodney J Folz

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Exercise improves angiogenic function of circulating exosomes in type 2 diabetes: Role of exosomal SOD3.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  3. The Role of Histone Protein Acetylation in Regulating Endothelial Function.Frontiers in cell and developmental biology · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. Extracellular superoxide dismutase and its role in cancer.Free radical biology & medicine · 2017
    Review
  8. Tumor necrosis factor-α decreases EC-SOD expression through DNA methylation.Journal of clinical biochemistry and nutrition · 2017
    Article
  9. Article
  10. Article
  11. Extracellular Superoxide Dismutase: Growth Promoter or Tumor Suppressor?Oxidative medicine and cellular longevity · 2016
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. 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

4 authors at 2 institutions in 1 country.

Igor N ZelkoDepartment of Medicine, University of Louisville, KY 40202, USA. igor.zelko@louisville.edu
Marcus W Stepp
Alan L Vorst
Rodney J Folz
University of Louisville · USUniversity of Louisville Hospital · US

Funding

REGULATION AND FUNCTION OF EC-SODR01HL064894 · NHLBI · UNIVERSITY OF LOUISVILLE · PI FOLZ, RODNEY J · 2000 to 2009
$2.7M
Mechanisms of lung injury following autologous BMTR01HL074289 · NHLBI · UNIVERSITY OF LOUISVILLE · PI FOLZ, RODNEY J · 2003 to 2006
$1.5M
NHLBI NIH HHS HL074289NHLBI NIH HHS HL64894NHLBI NIH HHS R01 HL064894NHLBI NIH HHS R01 HL074289
6 · The paper itself

Abstract

Extracellular superoxide dismutase (EC-SOD) is the major antioxidant enzyme present in the vascular wall, and is responsible for both the protection of vessels from oxidative stress and for the modulation of vascular tone. Concentrations of EC-SOD in human pulmonary arteries are very high relative to other tissues, and the expression of EC-SOD appears highly restricted to smooth muscle. The molecular basis for this smooth muscle-specific expression of EC-SOD is not known. Here we assessed the role of epigenetic factors in regulating the cell-specific and IFN-γ-inducible expression of EC-SOD in human pulmonary artery cells. The analysis of CpG site methylation within the promoter and coding regions of the EC-SOD gene demonstrated higher levels of DNA methylation within the distal promoter region in endothelial cells compared with smooth muscle cells. Exposure of both cell types to DNA demethylation agents reactivated the transcription of EC-SOD in endothelial cells alone. However, exposure to the histone deacetylase inhibitor trichostatin A (TSA) significantly induced EC-SOD gene expression in both endothelial cells and smooth muscle cells. Concentrations of EC-SOD mRNA were also induced up to 45-fold by IFN-γ in smooth muscle cells, but not in endothelial cells. The IFN-γ-dependent expression of EC-SOD was regulated by the Janus tyrosine kinase/signal transducers and activators of transcription proteins signaling pathway. Simultaneous exposure to TSA and IFN-γ produced a synergistic effect on the induction of EC-SOD gene expression, but only in endothelial cells. These findings provide strong evidence that EC-SOD cell-specific and IFN-γ-inducible expression in pulmonary artery cells is regulated, to a major degree, by epigenetic mechanisms that include histone acetylation and DNA methylation.

Indexed as

AcetylationCpG IslandsDNA MethylationEndothelial CellsEpigenesis, GeneticGene Expression Regulation, EnzymologicHistone Deacetylase InhibitorsHistonesHumansHydroxamic AcidsInterferon-gammaJanus KinasesMuscle, Smooth, VascularPromoter Regions, GeneticPulmonary ArterySTAT Transcription FactorsHistone Deacetylase InhibitorsHistonesHydroxamic AcidsInterferon-gammaJanus KinasesSTAT Transcription FactorsSuperoxide Dismutasetrichostatin A

Identifiers

PMID21493784
PMCPMC3262691
OpenAlexW2040314752

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.