Evidence map›Paper›PMID 20193674›Full record

ArticleDevelopmental biology2010

Hedgehog signaling induces arterial endothelial cell formation by repressing venous cell fate.

Charles Williams, Seok-Hyung Kim, Terri T Ni, Lauren Mitchell, Hyunju Ro, John S Penn, Scott H Baldwin, Lila Solnica-Krezel, Tao P Zhong

Abstract read
In one paragraph

Article in Developmental biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

36 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Nile Tilapia (International journal of molecular sciences · 2024
    Article
  5. Article
  6. Article
  7. Review
  8. Veins and Arteries Build Hierarchical Branching Patterns Differently: Bottom-Up versus Top-Down.BioEssays : news and reviews in molecular, cellular and developmental biology · 2019
    Review
  9. Review
  10. Review
  11. Crosstalk between Stem and Progenitor Cellular Mediators with Special Emphasis on Vasculogenesis.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2017
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Endothelial cilia are essential for developmental vascular integrity in zebrafish.Journal of the American Society of Nephrology : JASN · 2015
    Article
  20. Keeping an eye on SOXC proteins.Developmental dynamics : an official publication of the American Association of Anatomists · 2015
    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

9 authors at 1 institution in 1 country.

Charles WilliamsDepartment of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37203, USA.
Seok-Hyung Kim
Terri T Ni
Lauren Mitchell
Hyunju Ro
John S Penn
Scott H Baldwin
Lila Solnica-Krezel
Tao P Zhong
Vanderbilt University · US

Funding

GENETIC ANALYSIS OF CONVERGENT EXTENSION IN ZEBRAFISHR01GM055101 · NIGMS · WASHINGTON UNIVERSITY · PI SOLNICAKREZEL, LILIANNA · 1997 to 2014
$4.5M
G alpha 12/13 Signaling in Zebrafish EmbryogenesisR01GM077770 · NIGMS · WASHINGTON UNIVERSITY · PI SOLNICAKREZEL, LILIANNA · 2006 to 2015
$1.9M
Notch-Gridlock Signaling in Vascular SpecificationR01HL073348 · NHLBI · VANDERBILT UNIVERSITY · PI ZHONG, TAO P · 2004 to 2008
$1.5M
NHLBI NIH HHS R01 HL073348NHLBI NIH HHS R01HL073348NIGMS NIH HHS R01 GM055101NIGMS NIH HHS R01GM055101NIGMS NIH HHS R01 GM077770
6 · The paper itself

Abstract

In vertebrate embryos, the dorsal aorta and the posterior cardinal vein form in the trunk to comprise the original circulatory loop. Previous studies implicate Hedgehog (Hh) signaling in the development of the dorsal aorta. However, the mechanism controlling specification of artery versus vein remains unclear. Here, we investigated the cell-autonomous mechanism of Hh signaling in angioblasts (endothelial progenitor cells) during arterial-venous specification utilizing zebrafish mutations in Smoothened (Smo), a G protein-coupled receptor essential for Hh signaling. smo mutants exhibit an absence of the dorsal aorta accompanied by a reciprocal expansion of the posterior cardinal vein. The increased number of venous cells is equivalent to the loss of arterial cells in embryos with loss of Smo function. Activation of Hh signaling expands the arterial cell population at the expense of venous cell fate. Time-lapse imaging reveals two sequential waves of migrating progenitor cells that contribute to the dorsal aorta and the posterior cardinal vein, respectively. Angioblasts deficient in Hh signaling fail to contribute to the arterial wave; instead, they all migrate medially as a single population to form the venous wave. Cell transplantation analyses demonstrate that Smo plays a cell-autonomous role in specifying angioblasts to become arterial cells, and Hh signaling-depleted angioblasts differentiate into venous cells instead. Collectively, these studies suggest that arterial endothelial cells are specified and formed via repressing venous cell fate at the lateral plate mesoderm by Hh signaling during vasculogenesis.

Indexed as

Signal TransductionAnimalsArteriesEmbryo, NonmammalianEndothelial CellsHedgehog ProteinsReceptors, G-Protein-CoupledSmoothened ReceptorVeinsZebrafishZebrafish ProteinsHedgehog ProteinsReceptors, G-Protein-CoupledSmoothened Receptorsmo protein, zebrafishZebrafish Proteins

Identifiers

PMID20193674
PMCPMC3197743
OpenAlexW2067250618

What OpenQuestion holds

Textmetadata
LicenceTDM
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.