Evidence map›Paper›PMID 36639367›Full record

ArticleNature communications2023

Multiple pkd and piezo gene family members are required for atrioventricular valve formation.

Thomas Juan, Agatha Ribeiro da Silva, Bárbara Cardoso, SoEun Lim, Violette Charteau, Didier Y R Stainier

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 21 citations in OpenAlex.

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  10. Coordination of cardiogenesis in vivo and in vitro.Nature reviews. Molecular cell biology · 2026
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Zebrafish Congenital Heart Disease Models: Opportunities and Challenges.International journal of molecular sciences · 2024
    Review
  16. Science advances · 2024
    Article
  17. Review
  18. Article
  19. 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 at 2 institutions in 2 countries.

Thomas JuanMax Planck Institute for Heart and Lung Research, Department of Developmental Genetics, Bad Nauheim, Germany. thomas.juan@mpi-bn.mpg.de.ORCID 0000-0002-9654-3717
Agatha Ribeiro da Silva *Max Planck Institute for Heart and Lung Research, Department of Developmental Genetics, Bad Nauheim, Germany.
Bárbara Cardoso *Max Planck Institute for Heart and Lung Research, Department of Developmental Genetics, Bad Nauheim, Germany.
SoEun LimMax Planck Institute for Heart and Lung Research, Department of Developmental Genetics, Bad Nauheim, Germany.ORCID 0000-0003-2828-9734
Violette CharteauMax Planck Institute for Heart and Lung Research, Department of Developmental Genetics, Bad Nauheim, Germany.
Didier Y R StainierMax Planck Institute for Heart and Lung Research, Department of Developmental Genetics, Bad Nauheim, Germany. didier.stainier@mpi-bn.mpg.de.ORCID 0000-0002-0382-0026
Max Planck Institute for Heart and Lung Research · DERadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac valves ensure unidirectional blood flow through the heart, and altering their function can result in heart failure. Flow sensing via wall shear stress and wall stretching through the action of mechanosensors can modulate cardiac valve formation. However, the identity and precise role of the key mechanosensors and their effectors remain mostly unknown. Here, we genetically dissect the role of Pkd1a and other mechanosensors in atrioventricular (AV) valve formation in zebrafish and identify a role for several pkd and piezo gene family members in this process. We show that Pkd1a, together with Pkd2, Pkd1l1, and Piezo2a, promotes AV valve elongation and cardiac morphogenesis. Mechanistically, Pkd1a, Pkd2, and Pkd1l1 all repress the expression of klf2a and klf2b, transcription factor genes implicated in AV valve development. Furthermore, we find that the calcium-dependent protein kinase Camk2g is required downstream of Pkd function to repress klf2a expression. Altogether, these data identify, and dissect the role of, several mechanosensors required for AV valve formation, thereby broadening our understanding of cardiac valvulogenesis.

Indexed as

Heart ValvesZebrafishAnimalsAnimals, Genetically ModifiedOrganogenesisZebrafish ProteinsZebrafish Proteins

Identifiers

PMID36639367
PMCPMC9839778
OpenAlexW4315880960

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.