Evidence map›Paper›PMID 21984378›Full record

ArticleAmino acids2013

Nitric oxide regulates tissue transglutaminase localization and function in the vasculature.

Simran K Jandu, Alanah K Webb, Alina Pak, Baris Sevinc, Daniel Nyhan, Alexey M Belkin, Nicholas A Flavahan, Dan E Berkowitz, Lakshmi Santhanam

Open access · greenAbstract read
In one paragraph

Article in Amino acids, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Sitting leg vasculopathy: potential adaptations beyond the endothelium.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  7. Review
  8. Role of adropin in arterial stiffening associated with obesity and type 2 diabetes.American journal of physiology. Heart and circulatory physiology · 2022
    Article
  9. Article
  10. Article
  11. Spotlight on the Transglutaminase 2-Heparan Sulfate Interaction.Medical sciences (Basel, Switzerland) · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Exercise, vascular stiffness, and tissue transglutaminase.Journal of the American Heart Association · 2014
    Article
  18. Review
  19. Review
  20. Increased tissue transglutaminase activity contributes to central vascular stiffness in eNOS knockout mice.American journal of physiology. Heart and circulatory physiology · 2013
    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

9 authors at 3 institutions in 1 country.

Simran K JanduDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, 720 Rutland Ave, Ross 1150, Baltimore, MD 21205, USA.
Alanah K Webb
Alina Pak
Baris Sevinc
Daniel Nyhan
Alexey M Belkin
Nicholas A Flavahan
Dan E Berkowitz
Lakshmi Santhanam
Johns Hopkins Medicine · USJohns Hopkins University · USUniversity of Maryland, Baltimore · US

Funding

Transglutaminase 2 S-Nitrosylation: Role in Age-Related Vascular StiffnessR01HL105296 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI BERKOWITZ, DAN E · 2010 to 2013
$1.6M
NHLBI NIH HHS 1R01-HL105296-01NHLBI NIH HHS R01 HL105296
6 · The paper itself

Abstract

The multifunctional enzyme tissue transglutaminase (TG2) contributes to the development and progression of several cardiovascular diseases. Extracellular rather than intracellular TG2 is enzymatically active, however, the mechanism by which it is exported out of the cell remains unknown. Nitric oxide (NO) is shown to constrain TG2 externalization in endothelial and fibroblast cells. Here, we examined the role of both exogenous and endogenous (endothelial cell-derived) NO in regulating TG2 localization in vascular cells and tissue. NO synthase inhibition in endothelial cells (ECs) using N-nitro L-arginine methyl ester (L-NAME) led to a time-dependent decrease in S-nitrosation and increase in externalization of TG2. Laminar shear stress led to decreased extracellular TG2 in ECs. S-nitrosoglutathione treatment led to decreased activity and externalization of TG2 in human aortic smooth muscle and fibroblast (IMR90) cells. Co-culture of these cells with ECs resulted in increased S-nitrosation and decreased externalization and activity of TG2, which was reversed by L-NAME. Aged Fischer 344 rats had higher tissue scaffold-associated TG2 compared to young. NO regulates intracellular versus extracellular TG2 localization in vascular cells and tissue, likely via S-nitrosation. This in part, explains increased TG2 externalization and activity in aging aorta.

Indexed as

Age FactorsAnimalsAortaCell LineCoculture TechniquesEndothelial CellsEndothelium, VascularExtracellular MatrixFibroblastsGTP-Binding ProteinsHumansMyocytes, Smooth MuscleNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide Synthase Type IIINitrosationGTP-Binding ProteinsNG-Nitroarginine Methyl EsterNitric OxideNitric Oxide Synthase Type IIINOS3 protein, humanProtein Glutamine gamma Glutamyltransferase 2Tgm2 protein, ratTransglutaminases

Identifiers

PMID21984378
PMCPMC3744185
OpenAlexW1997979647

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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.