Evidence map›Paper›PMID 24058412›Full record

ArticlePloS one2013

Cardiac myocyte diversity and a fibroblast network in the junctional region of the zebrafish heart revealed by transmission and serial block-face scanning electron microscopy.

Pascal J Lafontant, Ali R Behzad, Evelyn Brown, Paul Landry, Norman Hu, Alan R Burns

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Modulation of VEGFA Signaling During Heart Regeneration in Zebrafish.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Reactive oxygen species during heart regeneration in zebrafish: Lessons for future clinical therapies.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society · 2021
    Review
  11. Cauterization as a Simple Method for Regeneration Studies in the Zebrafish Heart.Journal of cardiovascular development and disease · 2020
    Article
  12. Living myofibroblast-silicon composites for probing electrical coupling in cardiac systems.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  13. Article
  14. The epicardium as a hub for heart regeneration.Nature reviews. Cardiology · 2018
    Review
  15. Transient fibrosis resolves via fibroblast inactivation in the regenerating zebrafish heart.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  16. Article
  17. Deletion of Pr130 Interrupts Cardiac Development in Zebrafish.International journal of molecular sciences · 2016
    Article
  18. Article
  19. Differential Lectin Binding Patterns Identify Distinct Heart Regions in Giant Danio ( Devario aequipinnatus) and Zebrafish ( Danio rerio) Hearts.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2016
    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

6 authors.

Pascal J LafontantDepartment of Biology, DePauw University, Greencastle, Indiana, United States of America.
Ali R Behzad
Evelyn Brown
Paul Landry
Norman Hu
Alan R Burns

Funding

Research Programming ModuleP30EY007551 · NEI · UNIVERSITY OF HOUSTON · PI VALLABH E DAS · 1988 to 2026
$16.4M
Leukocyte Migration in Wounded CorneaR01EY017120 · NEI · UNIVERSITY OF HOUSTON · PI BURNS, ALAN R · 2007 to 2011
$1.8M
NEI NIH HHS EY017120NEI NIH HHS P30 EY007551NEI NIH HHS P30EY007551NEI NIH HHS R01 EY017120
6 · The paper itself

Abstract

The zebrafish has emerged as an important model of heart development and regeneration. While the structural characteristics of the developing and adult zebrafish ventricle have been previously studied, little attention has been paid to the nature of the interface between the compact and spongy myocardium. Here we describe how these two distinct layers are structurally and functionally integrated. We demonstrate by transmission electron microscopy that this interface is complex and composed primarily of a junctional region occupied by collagen, as well as a population of fibroblasts that form a highly complex network. We also describe a continuum of uniquely flattened transitional cardiac myocytes that form a circumferential plate upon which the radially-oriented luminal trabeculae are anchored. In addition, we have uncovered within the transitional ring a subpopulation of markedly electron dense cardiac myocytes. At discrete intervals the transitional cardiac myocytes form contact bridges across the junctional space that are stabilized through localized desmosomes and fascia adherentes junctions with adjacent compact cardiac myocytes. Finally using serial block-face scanning electron microscopy, segmentation and volume reconstruction, we confirm the three-dimensional nature of the junctional region as well as the presence of the sheet-like fibroblast network. These ultrastructural studies demonstrate the previously unrecognized complexity with which the compact and spongy layers are structurally integrated, and provide a new basis for understanding development and regeneration in the zebrafish heart.

Indexed as

AnimalsCollagenFibroblastsMicroscopy, Electron, ScanningMicroscopy, Electron, TransmissionMyocardiumMyocytes, CardiacZebrafishCollagen

Identifiers

PMID24058412
PMCPMC3751930

What OpenQuestion holds

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LicenceCC BY
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.