Evidence map›Paper›PMID 33082351›Full record

ArticleNature communications2020

Nkx2-5 defines distinct scaffold and recruitment phases during formation of the murine cardiac Purkinje fiber network.

Caroline Choquet, Robert G Kelly, Lucile Miquerol

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Immune-mediated cardiac development and regeneration.Seminars in cell & developmental biology · 2025
    Review
  3. Article
  4. The molecular mechanisms of cardiac development and related diseases.Signal transduction and targeted therapy · 2024
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Molecular Pathways and Animal Models of Arrhythmias.Advances in experimental medicine and biology · 2024
    Article
  13. Development of the Cardiac Conduction System.Advances in experimental medicine and biology · 2024
    Article
  14. DbhNature communications · 2023
    Article
  15. Article
  16. Article
  17. Journal of cardiovascular development and disease · 2023
    Article
  18. Review
  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

3 authors at 1 institution in 1 country.

Caroline ChoquetAix-Marseille Université, CNRS UMR 7288, Developmental Biology Institute of Marseille, Campus de Luminy Case 907, 13288, Marseille, Cedex 9, France.ORCID 0000-0002-4760-6793
Robert G KellyAix-Marseille Université, CNRS UMR 7288, Developmental Biology Institute of Marseille, Campus de Luminy Case 907, 13288, Marseille, Cedex 9, France.
Lucile MiquerolAix-Marseille Université, CNRS UMR 7288, Developmental Biology Institute of Marseille, Campus de Luminy Case 907, 13288, Marseille, Cedex 9, France. lucile.miquerol@univ-amu.fr.ORCID 0000-0002-2776-5914
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ventricular conduction system coordinates heartbeats by rapid propagation of electrical activity through the Purkinje fiber (PF) network. PFs share common progenitors with contractile cardiomyocytes, yet the mechanisms of segregation and network morphogenesis are poorly understood. Here, we apply genetic fate mapping and temporal clonal analysis to identify murine cardiomyocytes committed to the PF lineage as early as E7.5. We find that a polyclonal PF network emerges by progressive recruitment of conductive precursors to this scaffold from a pool of bipotent progenitors. At late fetal stages, the segregation of conductive cells increases during a phase of rapid recruitment to build the definitive PF network through a non-cell autonomous mechanism. We also show that PF differentiation is impaired in Nkx2-5 haploinsufficient embryos leading to failure to extend the scaffold. In particular, late fetal recruitment fails, resulting in PF hypoplasia and persistence of bipotent progenitors. Our results identify how transcription factor dosage regulates cell fate divergence during distinct phases of PF network morphogenesis.

Indexed as

AnimalsFemaleGene Expression Regulation, DevelopmentalHeartHomeobox Protein Nkx-2.5MaleMiceMorphogenesisMyocytes, CardiacPurkinje FibersHomeobox Protein Nkx-2.5Nkx2-5 protein, mouse

Identifiers

PMID33082351
PMCPMC7575572
OpenAlexW3093480536

What OpenQuestion holds

Textmetadata
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.