Evidence map›Paper›PMID 20457832›Full record

ArticleAmerican journal of physiology. Cell physiology2010

Limitations of conventional approaches to identify myocyte nuclei in histologic sections of the heart.

Keng-Leong Ang, Lincoln T Shenje, Sean Reuter, Mark H Soonpaa, Michael Rubart, Loren J Field, Manuel Galiñanes

Open access · greenAbstract readComparative Study
In one paragraph

Article in American journal of physiology. Cell physiology, 2010. 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
1.6field-weighted citation impact, top 17% 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, 59 citations in OpenAlex.

  1. Mechanisms and Therapeutic Potential of Human Cardiomyocyte Proliferation.Journal of cardiovascular development and disease · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Measuring cardiomyocyte cell-cycle activity and proliferation in the age of heart regeneration.American journal of physiology. Heart and circulatory physiology · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Reptiles as a Model System to Study Heart Development.Cold Spring Harbor perspectives in biology · 2020
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. 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

7 authors at 3 institutions in 2 countries.

Keng-Leong AngDepartment of Cardiovascular Sciences, University of Leicester, UK.
Lincoln T Shenje
Sean Reuter
Mark H Soonpaa
Michael Rubart
Loren J Field
Manuel Galiñanes
Indiana University School of MedicineGlenfield Hospital · GBUniversity of Leicester · GB

Funding

REGULATION OF CARDIOMYOCYTE SURVIVALP01HL085098 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FIRULLI, ANTHONY B. · 2007 to 2011
$10.9M
Genetic Enhancement of Cardiac Repair with Adult Stem CellsR01HL083126 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FIELD, LOREN J · 2006 to 2015
$2.9M
NHLBI NIH HHS P01 HL085098NHLBI NIH HHS R01 HL083126
6 · The paper itself

Abstract

Accurate nuclear identification is crucial for distinguishing the role of cardiac myocytes in intrinsic and experimentally induced regenerative growth of the myocardium. Conventional histologic analysis of myocyte nuclei relies on the optical sectioning capabilities of confocal microscopy in conjunction with immunofluorescent labeling of cytoplasmic proteins such as troponin T, and dyes that bind to double-strand DNA to identify nuclei. Using heart sections from transgenic mice in which the cardiomyocyte-restricted alpha-cardiac myosin heavy chain promoter targeted the expression of nuclear localized beta-galactosidase reporter in >99% of myocytes, we systematically compared the fidelity of conventional myocyte nuclear identification using confocal microscopy, with and without the aid of a membrane marker. The values obtained with these assays were then compared with those obtained with anti-beta-galactosidase immune reactivity in the same samples. In addition, we also studied the accuracy of anti-GATA4 immunoreactivity for myocyte nuclear identification. Our results demonstrate that, although these strategies are capable of identifying myocyte nuclei, the level of interobserver agreement and margin of error can compromise accurate identification of rare events, such as cardiomyocyte apoptosis and proliferation. Thus these data indicate that morphometric approaches based on segmentation are justified only if the margin of error for measuring the event in question has been predetermined and deemed to be small and uniform. We also illustrate the value of a transgene-based approach to overcome these intrinsic limitations of identifying myocyte nuclei. This latter approach should prove quite useful when measuring rare events.

Indexed as

ImmunohistochemistryMicroscopy, ConfocalAnimalsbeta-GalactosidaseBiomarkersCardiac MyosinsCell NucleusCell ProliferationGATA4 Transcription FactorGenes, ReporterMiceMice, Inbred DBAMice, TransgenicMyocytes, CardiacMyosin Heavy ChainsObserver Variationbeta-GalactosidaseBiomarkersCardiac MyosinsGata4 protein, mouseGATA4 Transcription FactorMyosin Heavy ChainsTroponin TWheat Germ Agglutinins

Identifiers

PMID20457832
PMCPMC2902296
OpenAlexW2045523675

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.