Evidence map›Paper›PMID 24415751›Full record

Trial reportThe Journal of biological chemistry2014

Calcineurin-NFATc regulates type 2 inositol 1,4,5-trisphosphate receptor (InsP3R2) expression during cardiac remodeling.

Natesan Sankar, Pieter P deTombe, Gregory A Mignery

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

29 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Potential Roles of IPBiomolecules · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. Function and Role of Histamine HPharmaceuticals (Basel, Switzerland) · 2023
    Review
  9. Article
  10. Article
  11. Inositol 1,4,5-trisphosphate receptors in cardiomyocyte physiology and disease.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Calcium Signaling in Cardiomyocyte Function.Cold Spring Harbor perspectives in biology · 2020
    Review
  17. Review
  18. Article
  19. Nuclear calcineurin is a sensor for detecting CaJournal of molecular medicine (Berlin, Germany) · 2018
    Article
  20. 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

3 authors at 1 institution in 1 country.

Natesan SankarFrom the Department of Cell & Molecular Physiology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois 60153.
Pieter P deTombe
Gregory A Mignery
Loyola University Chicago · US

Funding

Program AdministrationP01HL080101 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BERS, DONALD M · 2006 to 2015
$23.4M
NHLBI NIH HHS P01 HL080101NHLBI NIH HHS P01-HL080101
6 · The paper itself

Abstract

In heart, the type 2 inositol 1,4,5-triphosphate receptor (InsP3R2) is the predominant isoform expressed and is localized in the nuclear membrane of ventricular myocytes. InsP3R2-mediated Ca(2+) release regulates hypertrophy specific gene expression by modulating CaMKIIδ, histone deacetylase, and calcineurin-NFATc signaling pathways. InsP3R2 protein is a hypertrophy specific marker and is overexpressed in heart failure animal models and in humans. However, the regulation of InsP3R2 mRNA and protein expression during cardiac hypertrophy and heart failure is not known. Here we show the transcriptional regulation of the Itpr2 gene in adult cardiomyocytes. Our data demonstrates that, InsP3R2 mRNA and protein expression is activated by hypertrophic agonists and attenuated by InsP3R inhibitors 2-aminoethoxyldiphenyl borate and xestospongin-C. The Itpr2 promoter is regulated by the calcineurin-NFATc signaling pathway. NFATc1 regulates Itpr2 gene expression by directly binding to the Itpr2 promoter. The calcineurin-NFATc mediated up-regulation of the Itpr2 promoter was attenuated by cyclosporine-A. InsP3R2 mRNA and protein expression was up-regulated in calcineurin-A transgenic mice and in human heart failure. Collectively, our data suggests that ITPR2 and hypertrophy specific gene expression is regulated, in part, by a positive feedback regulation between InsP3R2 and calcineurin-NFATc signaling pathways.

Indexed as

Signal TransductionAdultAnimalsBoron CompoundsCalcineurinCalcium-Calmodulin-Dependent Protein Kinase Type 2CardiomegalyFemaleHeart FailureHumansInositol 1,4,5-Trisphosphate ReceptorsMacrocyclic CompoundsMaleMiceMyocytes, CardiacNFATC Transcription Factors2-aminoethyl diphenylborinateBoron CompoundsCalcineurinCalcium-Calmodulin-Dependent Protein Kinase Type 2Inositol 1,4,5-Trisphosphate ReceptorsITPR2 protein, humanITPR2 protein, ratMacrocyclic CompoundsNFATC1 protein, humanNfatc1 protein, mouseNFATC Transcription FactorsOxazolesxestospongin CCalcineurinCalcium SignalingCardiac HypertrophyGene TranscriptionInositol 1,4,5-Trisphosphate

Identifiers

PMID24415751
PMCPMC3937684
OpenAlexW2013609428

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.