Evidence map›Paper›PMID 23748970›Full record

ArticleNature communications2013

Haemodynamically dependent valvulogenesis of zebrafish heart is mediated by flow-dependent expression of miR-21.

Toshihiro Banjo, Janin Grajcarek, Daisuke Yoshino, Hideto Osada, Kota Y Miyasaka, Yasuyuki S Kida, Yosuke Ueki, Kazuaki Nagayama, Koichi Kawakami, Takeo Matsumoto and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Nature communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. Science advances · 2024
    Article
  3. Hemodynamics During Development and Postnatal Life.Advances in experimental medicine and biology · 2024
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Cardiac toxicity of acrolein exposure in embryonic zebrafish (Danio rerio).Environmental science and pollution research international · 2020
    Article
  16. Biomechanical Cues Direct Valvulogenesis.Journal of cardiovascular development and disease · 2020
    Review
  17. Review
  18. Fluid forces shape the embryonic heart: Insights from zebrafish.Current topics in developmental biology · 2019
    Review
  19. Epigenetic Regulation of Organ Regeneration in Zebrafish.Journal of cardiovascular development and disease · 2018
    Review
  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

12 authors at 5 institutions in 2 countries.

Toshihiro BanjoGraduate School of Life Sciences, Tohoku University, 2-1-1 Katahira, Aoba, Sendai, Miyagi 980-8577, Japan.
Janin Grajcarek
Daisuke Yoshino
Hideto Osada
Kota Y Miyasaka
Yasuyuki S Kida
Yosuke Ueki
Kazuaki Nagayama
Koichi Kawakami
Takeo Matsumoto
Masaaki Sato
Toshihiko Ogura
Tohoku University · JPNagoya Institute of Technology · JPHeidelberg University · DENational Institute of Advanced Industrial Science and Technology · JPNational Institute of Genetics · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heartbeat is required for normal development of the heart, and perturbation of intracardiac flow leads to morphological defects resembling congenital heart diseases. These observations implicate intracardiac haemodynamics in cardiogenesis, but the signalling cascades connecting physical forces, gene expression and morphogenesis are largely unknown. Here we use a zebrafish model to show that the microRNA, miR-21, is crucial for regulation of heart valve formation. Expression of miR-21 is rapidly switched on and off by blood flow. Vasoconstriction and increasing shear stress induce ectopic expression of miR-21 in the head vasculature and heart. Flow-dependent expression of mir-21 governs valvulogenesis by regulating the expression of the same targets as mouse/human miR-21 (sprouty, pdcd4, ptenb) and induces cell proliferation in the valve-forming endocardium at constrictions in the heart tube where shear stress is highest. We conclude that miR-21 is a central component of a flow-controlled mechanotransduction system in a physicogenetic regulatory loop.

Indexed as

Hemodynamics3' Untranslated RegionsAnimalsBase SequenceBlood CirculationButadienesDiacetylGene Expression Regulation, DevelopmentalHeart ValvesHEK293 CellsHumansMAP Kinase Signaling SystemMicroRNAsMolecular Sequence DataMorpholinosNitriles3' Untranslated RegionsButadienesDiacetyldiacetylmonoximeMicroRNAsMIRN21 microRNA, zebrafishMorpholinosNitrilesRNA, MessengerU 0126Zebrafish Proteins

Identifiers

PMID23748970
PMCPMC3709480
OpenAlexW1977358193

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.