Evidence map›Paper›PMID 25318477›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2015

E-NTPDase1/CD39 modulates renin release from heart mast cells during ischemia/reperfusion: a novel cardioprotective role.

Silvia Aldi, Alice Marino, Kengo Tomita, Federico Corti, Ranjini Anand, Kim E Olson, Aaron J Marcus, Roberto Levi

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Mast Cells in Cardiac Remodeling: Focus on the Right Ventricle.Journal of cardiovascular development and disease · 2024
    Review
  2. Mitochondrial Homeostasis and Mast Cells in Experimental Hepatic Ischemia-Reperfusion Injury of Rats.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2022
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. A Retinoic AcidThe Journal of pharmacology and experimental therapeutics · 2018
    Article
  11. Thirst sensation and oral dryness following alcohol intake.The Japanese dental science review · 2017
    Review
  12. Article
  13. The novel HBritish journal of pharmacology · 2016
    Article
  14. Aaron J. Marcus: in pursuit of perfection.The Journal of clinical investigation · 2015
    Article
  15. 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.

Silvia AldiDepartments of Pharmacology and.
Alice MarinoDepartments of Pharmacology and.
Kengo TomitaDepartments of Pharmacology and.
Federico CortiDepartments of Pharmacology and.
Ranjini AnandDivision of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medical College, New York, New York, USA; and Thrombosis Research Laboratory, Veterans Affairs New York Harbor Healthcare System, New York, New York, USA.
Kim E OlsonDivision of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medical College, New York, New York, USA; and Thrombosis Research Laboratory, Veterans Affairs New York Harbor Healthcare System, New York, New York, USA.
Aaron J MarcusPathology and Laboratory Medicine and Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medical College, New York, New York, USA; and Thrombosis Research Laboratory, Veterans Affairs New York Harbor Healthcare System, New York, New York, USA.
Roberto LeviDepartments of Pharmacology and rlevi@med.cornell.edu.
Cornell University · USVA NY Harbor Healthcare System · US

Funding

Disparities in COVID Disease Severity and Outcomes in New York CityUL1TR002384 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JULIANNE L IMPERATO-MCGINLEY · 2017 to 2026
$86.2M
Clinical and Translational Science CenterUL1TR000457 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI IMPERATO-MCGINLEY, JULIANNE L · 2012 to 2016
$46.0M
Histamine Receptor/Norepinephrine in Cardiac DysfunctionR01HL034215 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LEVI, ROBERTO · 1985 to 2013
$6.6M
Cell-Cell Interactions in Thrombosis -Request for Extension of Merit AwardR37HL047073 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MARCUS, AARON JACOB · 2004 to 2011
$3.7M
Cell-Cell Interactions in Thrombosis -Request for Extension of Merit AwardR01HL047073 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI DROSOPOULOS, JOAN H. F. · 1991 to 2014
$3.1M
Thromboregulation in Occlusive Vascular DiseasesR01HL089521 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MARCUS, AARON JACOB · 2009 to 2012
$2.9M
NCATS NIH HHS UL1 TR000457NCATS NIH HHS UL1 TR002384NHLBI NIH HHS HL034215NHLBI NIH HHS HL047073NHLBI NIH HHS HL047073-23S1NHLBI NIH HHS HL089521NHLBI NIH HHS R01 HL034215NHLBI NIH HHS R01 HL047073NHLBI NIH HHS R01 HL089521NHLBI NIH HHS R37 HL047073
6 · The paper itself

Abstract

Ischemia/reperfusion (I/R) elicits renin release from cardiac mast cells (MC), thus activating a local renin-angiotensin system (RAS), culminating in ventricular fibrillation. We hypothesized that in I/R, neurogenic ATP could degranulate juxtaposed MC and that ecto-nucleoside triphosphate diphosphohydrolase 1/CD39 (CD39) on MC membrane could modulate ATP-induced renin release. We report that pharmacological inhibition of CD39 in a cultured human mastocytoma cell line (HMC-1) and murine bone marrow-derived MC with ARL67156 (100 µM) increased ATP-induced renin release (≥2-fold), whereas purinergic P2X7 receptors (P2X7R) blockade with A740003 (3 µM) prevented it. Likewise, CD39 RNA silencing in HMC-1 increased ATP-induced renin release (≥2-fold), whereas CD39 overexpression prevented it. Acetaldehyde, an I/R product (300 µM), elicited an 80% increase in ATP release from HMC-1, in turn, causing an autocrine 20% increase in renin release. This effect was inhibited or potentiated when CD39 was overexpressed or silenced, respectively. Moreover, P2X7R silencing prevented ATP- and acetaldehyde-induced renin release. I/R-induced RAS activation in ex vivo murine hearts, characterized by renin and norepinephrine overflow and ventricular fibrillation, was potentiated (∼2-fold) by CD39 inhibition, an effect prevented by P2X7R blockade. Our data indicate that by regulating ATP availability at the MC surface, CD39 modulates local renin release and thus, RAS activation, ultimately exerting a cardioprotective effect.

Indexed as

Myocardial ReperfusionAdenosine TriphosphateAnimalsAntigens, CDApyraseCardiotonic AgentsCell DegranulationCell LineHumansMaleMast CellsMiceMice, Inbred C57BLMyocardiumReceptors, Purinergic P2X7Renin6-N,N-diethyl-beta,gamma-dibromomethylene-D-ATPAdenosine TriphosphateAntigens, CDApyraseCardiotonic AgentsCD39 antigenReceptors, Purinergic P2X7ReninRNA, Small InterferingarrhythmiasATPP2X7 purinergic receptorsrenin-angiotensin systemtoxic aldehydes

Identifiers

PMID25318477
PMCPMC4285537
OpenAlexW2090146004

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.