Evidence map›Paper›PMID 21922294›Full record

ArticleAngiogenesis2011

Chronic hypoxia impairs extracellular nucleotide metabolism and barrier function in pulmonary artery vasa vasorum endothelial cells.

Gennady G Yegutkin, Mikko Helenius, Elzbieta Kaczmarek, Nana Burns, Sirpa Jalkanen, Kurt Stenmark, Evgenia V Gerasimovskaya

Abstract read
In one paragraph

Article in Angiogenesis, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Astrocyte-neuron circuits in epilepsy.Neurobiology of disease · 2023
    Review
  5. Article
  6. Review
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  15. Article
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  17. 8-BuS-ATP derivatives as specific NTPDase1 inhibitors.British journal of pharmacology · 2013
    Article
  18. Article
  19. Metabolism of circulating ADP in the bloodstream is mediated via integrated actions of soluble adenylate kinase-1 and NTPDase1/CD39 activities.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    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

7 authors at 4 institutions in 2 countries.

Gennady G YegutkinMediCity Research Laboratory, University of Turku and National Institute of Health and Welfare, Tykistökatu 6A, 20520, Turku, Finland. genyeg@utu.fi
Mikko Helenius
Elzbieta Kaczmarek
Nana Burns
Sirpa Jalkanen
Kurt Stenmark
Evgenia V Gerasimovskaya
University of Colorado Denver · USUniversity of Turku · FIFinnish Institute for Health and Welfare · FIHarvard University · US

Funding

VRAC and Rho in pulmonary EC proliferationP01HL014985 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI STENMARK, KURT R. · 1985 to 2019
$35.1M
Extracellular ATP: potential regulator of hypoxia-induced vasa vasorum neovasculaR01HL086783 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI GERASIMOVSKAYA, EVGENIA V · 2008 to 2017
$4.2M
Fibroblasts and Mononuclear Fibrogenic Cells Drive Right Ventricular Pulmonary ArR01HL114887 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI BULL, TODD M, BUTTRICK, PETER N. · 2012 to 2016
$3.4M
NHLBI NIH HHS P01 HL014985NHLBI NIH HHS R01 HL086783NHLBI NIH HHS R01 HL114887
6 · The paper itself

Abstract

Vascular remodeling plays a pivotal role in a variety of pathophysiological conditions where hypoxia and inflammation are prominent features. Intravascular ATP, ADP and adenosine are known as important regulators of vascular tone, permeability and homeostasis, however contribution of purinergic signalling to endothelial cell growth and angiogenesis remains poorly understood. By using vasa vasorum endothelial cells (VVEC) isolated from pulmonary artery adventitia of control and chronically hypoxic neonatal calves, these studies were aimed to evaluate the effect of hypoxia on biochemical and functional properties of microvascular endothelial network at the sites of angiogenesis. In comparison with normoxic controls, VVEC from hypoxic animals are characterized by (1) drastically impaired nucleoside triphosphate diphosphohydrolase-1 (NTPDase-1/CD39) and ecto-5'-nucleotidase/CD73 activities with respective increases in basal extracellular ATP and ADP levels (2) higher proliferative responses to low micromolar concentrations of ATP and ADP; and (3) enhanced permeability and disordered adenosinergic control of vascular barrier function (measured as a paracellular flux of 70 kDa fluorescein isothiocyanate-dextran). Together, these results suggest that unique pattern of purine-mediated angiogenic activation and enhanced leakiness of VVEC from chronically hypoxic vessels may be defined by disordered endothelial nucleotide homeostasis at sites of active neovascularization.

Indexed as

5'-NucleotidaseAdenosineAdenosine DiphosphateAdenosine TriphosphateAnalysis of VarianceAnimalsAnimals, NewbornAntigens, CDApyraseBlotting, WesternCapillary PermeabilityCattleCell ProliferationCyclic AMPDextransDNA Primers5'-NucleotidaseAdenosineAdenosine DiphosphateAdenosine TriphosphateAntigens, CDApyraseCD39 antigenCyclic AMPDextransDNA PrimersFluorescein-5-isothiocyanatefluorescein isothiocyanate dextran

Identifiers

PMID21922294
PMCPMC3940057
OpenAlexW1968821491

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.