Evidence map›Paper›PMID 26989176›Full record

ArticleDevelopment (Cambridge, England)2016

Multicolor mapping of the cardiomyocyte proliferation dynamics that construct the atrium.

Matthew J Foglia, Jingli Cao, Valerie A Tornini, Kenneth D Poss

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Animal models to study cardiac regeneration.Nature reviews. Cardiology · 2024
    Review
  4. Article
  5. Clonal Tracing of Heart Regeneration.Journal of cardiovascular development and disease · 2022
    Review
  6. Review
  7. Article
  8. Atrial and Sinoatrial Node Development in the Zebrafish Heart.Journal of cardiovascular development and disease · 2021
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Vegfaa instructs cardiac muscle hyperplasia in adult zebrafish.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Matthew J FogliaDepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Jingli CaoDepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Valerie A TorniniDepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Kenneth D PossDepartment of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA kenneth.poss@duke.edu.
Duke University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Training Program in Developmental & Stem Cell BiologyT32HD040372 · NICHD · DUKE UNIVERSITY · PI Terry H Lechler · 2001 to 2026
$8.9M
Regulation of Myocardial Regeneration in ZebrafishR01HL081674 · NHLBI · DUKE UNIVERSITY · PI POSS, KENNETH D · 2005 to 2019
$6.6M
Vegf Signaling and Cardiac Chamber Morphogenesis in ZebrafishF30HL126487 · NHLBI · DUKE UNIVERSITY · PI FOGLIA, MATTHEW J · 2015 to 2016
$68k
NHLBI NIH HHS F30 HL126487NHLBI NIH HHS R01 HL081674NICHD NIH HHS T32 HD040372NIGMS NIH HHS T32 GM007171
6 · The paper itself

Abstract

The orchestrated division of cardiomyocytes assembles heart chambers of distinct morphology. To understand the structural divergence of the cardiac chambers, we determined the contributions of individual embryonic cardiomyocytes to the atrium in zebrafish by multicolor fate-mapping and we compare our analysis to the established proliferation dynamics of ventricular cardiomyocytes. We find that most atrial cardiomyocytes become rod-shaped in the second week of life, generating a single-muscle-cell-thick myocardial wall with a striking webbed morphology. Inner pectinate myofibers form mainly by direct branching, unlike delamination events that create ventricular trabeculae. Thus, muscle clones assembling the atrial chamber can extend from wall to lumen. As zebrafish mature, atrial wall cardiomyocytes proliferate laterally to generate cohesive patches of diverse shapes and sizes, frequently with dominant clones that comprise 20-30% of the wall area. A subpopulation of cardiomyocytes that transiently express atrial myosin heavy chain (amhc) contributes substantially to specific regions of the ventricle, suggesting an unappreciated level of plasticity during chamber formation. Our findings reveal proliferation dynamics and fate decisions of cardiomyocytes that produce the distinct architecture of the atrium.

Indexed as

Imaging, Three-DimensionalAnimalsAnimals, Genetically ModifiedCell ProliferationClone CellsFemaleHeart AtriaHeart VentriclesLarvaMaleMusclesMyocardiumMyocytes, CardiacStaining and LabelingZebrafishAtriumBrainbowCardiomyocyteClonal analysisHeart developmentZebrafish

Identifiers

PMID26989176
PMCPMC4874486
OpenAlexW2297974985

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.