Evidence map›Paper›PMID 22919071›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2012

Telomerase expression in the mammalian heart.

Gavin D Richardson, David Breault, Grace Horrocks, Suzanne Cormack, Nicholas Hole, W Andrew Owens

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.5field-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

33 citing papers in PubMed, 70 citations in OpenAlex.

  1. Hypertension (Dallas, Tex. : 1979) · 2026
    Article
  2. Migrasomes in Ischemic Stroke: Molecular Landscape and Pathophysiological Impact.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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  20. Mitochondria, Telomeres and Telomerase Subunits.Frontiers in cell and developmental biology · 2019
    Review
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

6 authors at 4 institutions in 2 countries.

Gavin D RichardsonInstitute of Genetic Medicine, International Centre for Life, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK. gavin.richardson2@ncl.ac.uk
David Breault
Grace Horrocks
Suzanne Cormack
Nicholas Hole
W Andrew Owens
Durham University · GBHarvard Stem Cell Institute · USNewcastle University · GBSouth Tees Hospitals NHS Foundation Trust · GB

Funding

Characterization of Telomerase Expressing Intestinal Stem CellsR01DK084056 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI BREAULT, DAVID T · 2010 to 2015
$2.2M
British Heart Foundation PG/06/110/21521NIDDK NIH HHS R01 DK084056
6 · The paper itself

Abstract

While the mammalian heart has low, but functionally significant, levels of telomerase expression, the cellular population responsible remains incompletely characterized. This study aimed to identify the cell types responsible for cardiac telomerase activity in neonatal, adult, and cryoinjured adult hearts using transgenic mice expressing green fluorescent protein (GFP), driven by the promoter for murine telomerase reverse transcriptase (mTert), which is a necessary and rate-limiting component of telomerase. A rare population of mTert-GFP-expressing cells was identified that possessed all detectable cardiac telomerase RNA and telomerase activity. It was heterogeneous and included cells coexpressing markers of cardiomyocytic, endothelial, and mesenchymal lineages, putative cardiac stem cell markers, and, interestingly, cardiomyocytes with a differentiated phenotype. Quantification using both flow cytometry and immunofluorescence identified a significant decline in mTert-GFP cells in adult animals compared to neonates (∼9- and ∼20-fold, respectively). Cardiac injury resulted in a ∼6.45-fold expansion of this population (P<0.005) compared with sham-operated controls. This study identifies the cells responsible for cardiac telomerase activity, demonstrates a significant diminution with age but a marked response to injury, and, given the relationship between telomerase activity and stem cell populations, suggests that they represent a potential target for further investigation of cardiac regenerative potential.

Indexed as

Gene Expression Regulation, DevelopmentalGene Expression Regulation, EnzymologicAge FactorsAnimalsAnimals, NewbornAntigens, LyFlow CytometryGATA4 Transcription FactorGreen Fluorescent ProteinsHomeobox Protein Nkx-2.5Homeodomain ProteinsMembrane ProteinsMiceMice, TransgenicMicroscopy, ConfocalMyocardiumAntigens, LyGata4 protein, mouseGATA4 Transcription FactorGreen Fluorescent ProteinsHomeobox Protein Nkx-2.5Homeodomain ProteinsLy6a protein, mouseMembrane ProteinsNkx2-5 protein, mouseRNA, MessengerTelomeraseTert protein, mouseTranscription Factors

Identifiers

PMID22919071
PMCPMC3509052
OpenAlexW2018559644

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.