Evidence map›Paper›PMID 26769101›Full record

ArticleDevelopmental biology2016

Vegfa signaling promotes zebrafish intestinal vasculature development through endothelial cell migration from the posterior cardinal vein.

Andrew L Koenig, Kristina Baltrunaite, Neil I Bower, Andrea Rossi, Didier Y R Stainier, Benjamin M Hogan, Saulius Sumanas

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Lineage labeling with zebrafish hand2 Cre and CreERT2 recombinase CRISPR knock-ins.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  4. Article
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  6. Lineage labeling with zebrafishbioRxiv : the preprint server for biology · 2024
    Article
  7. Article
  8. Article
  9. Endothelial cell transitions in zebrafish vascular development.Development, growth & differentiation · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Modulation of VEGFA Signaling During Heart Regeneration in Zebrafish.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  17. Article
  18. Frontiers in cell and developmental biology · 2021
    Article
  19. Inhibitory Effects ofEvidence-based complementary and alternative medicine : eCAM · 2021
    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

7 authors at 3 institutions in 3 countries.

Andrew L KoenigDivision of Developmental Biology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA. Electronic address: andrew.koenig@cchmc.org.
Kristina BaltrunaiteDivision of Developmental Biology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA. Electronic address: kristina.baltrunaite@cchmc.org.
Neil I BowerDivision of Genomics of Development and Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4073, Australia. Electronic address: n.bower@imb.uq.edu.au.
Andrea RossiDepartment of Developmental Genetics, Max Planck Institute for Heart and Lung Research, Bad Nauheim 61231, Germany. Electronic address: andrea.rossi@mpi-bn.mpg.de.
Didier Y R StainierDepartment of Developmental Genetics, Max Planck Institute for Heart and Lung Research, Bad Nauheim 61231, Germany. Electronic address: didier.stainier@mpi-bn.mpg.de.
Benjamin M HoganDivision of Genomics of Development and Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4073, Australia. Electronic address: b.hogan@imb.uq.edu.au.
Saulius SumanasDivision of Developmental Biology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA. Electronic address: saulius.sumanas@cchmc.org.
Cincinnati Children's Hospital Medical Center · USMax Planck Institute for Heart and Lung Research · DEThe University of Queensland · AU

Funding

Understanding Cardiovascular Disease MechanismsT32HL125204 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI Evangelia G Kranias, Jeffery D Molkentin · 2015 to 2026
$3.4M
Molecular Mechanisms of Arterial-Venous Differentiation in ZebrafishR01HL107369 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI SUMANAS, SAULIUS · 2011 to 2015
$1.9M
NHLBI NIH HHS NIHR01HL107369NHLBI NIH HHS NIHT32HL125204NHLBI NIH HHS R01 HL107369NHLBI NIH HHS T32 HL125204
6 · The paper itself

Abstract

The mechanisms underlying organ vascularization are not well understood. The zebrafish intestinal vasculature forms early, is easily imaged using transgenic lines and in-situ hybridization, and develops in a stereotypical pattern thus making it an excellent model for investigating mechanisms of organ specific vascularization. Here, we demonstrate that the sub-intestinal vein (SIV) and supra-intestinal artery (SIA) form by a novel mechanism from angioblasts that migrate out of the posterior cardinal vein and coalesce to form the intestinal vasculature in an anterior to posterior wave with the SIA forming after the SIV. We show that vascular endothelial growth factor aa (vegfaa) is expressed in the endoderm at the site where intestinal vessels form and therefore likely provides a guidance signal. Vegfa/Vegfr2 signaling is required for early intestinal vasculature development with mutation in vegfaa or loss of Vegfr2 homologs causing nearly complete inhibition of the formation of the intestinal vasculature. Vegfc and Vegfr3 function, however, are dispensable for intestinal vascularization. Interestingly, ubiquitous overexpression of Vegfc resulted in an overgrowth of the SIV, suggesting that Vegfc is sufficient to induce SIV development. These results argue that Vegfa signaling directs endothelial cells to migrate out of existing vasculature and coalesce to form the intestinal vessels. It is likely that a similar mechanism is utilized during vascularization of other organs.

Indexed as

AnimalsAnimals, Genetically ModifiedCell MovementEndothelial CellsGene Expression Regulation, DevelopmentalGene Knockdown TechniquesIntestinesMorpholinosNeovascularization, PhysiologicSignal TransductionVascular Endothelial Growth Factor AVascular Endothelial Growth Factor CVascular Endothelial Growth Factor Receptor-2Vascular Endothelial Growth Factor Receptor-3ZebrafishZebrafish ProteinsMorpholinosVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Cvascular endothelial growth factor C, zebrafishVascular Endothelial Growth Factor Receptor-2Vascular Endothelial Growth Factor Receptor-3Zebrafish ProteinsIntestinalOrganVascular endothelialVegfZebrafish

Identifiers

PMID26769101
PMCPMC4769896
OpenAlexW2224707264

What OpenQuestion holds

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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.