Evidence map›Paper›PMID 23812297›Full record

ArticleCardiovascular research2013

Blood flow suppresses vascular Notch signalling via dll4 and is required for angiogenesis in response to hypoxic signalling.

Oliver Watson, Peter Novodvorsky, Caroline Gray, Alexander M K Rothman, Allan Lawrie, David C Crossman, Andrea Haase, Kathryn McMahon, Martin Gering, Fredericus J M Van Eeden and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Cardiovascular research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 54 citations in OpenAlex.

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  14. Mechanosensitivity of Jagged-Notch signaling can induce a switch-type behavior in vascular homeostasis.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  15. Flow Induced Microvascular Network Formation of Therapeutic Relevant Arteriovenous (AV) Loop-Based Constructs in Response to Ionizing Radiation.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
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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

11 authors at 2 institutions in 1 country.

Oliver WatsonLab D38, MRC Centre for Developmental and Biomedical Genetics, University of Sheffield, Firth Court, Sheffield S10 2TN, UK.
Peter Novodvorsky
Caroline Gray
Alexander M K Rothman
Allan Lawrie
David C Crossman
Andrea Haase
Kathryn McMahon
Martin Gering
Fredericus J M Van Eeden
Timothy J A Chico
University of Sheffield · GBUniversity of Nottingham · GB

Funding

British Heart Foundation PG/13/2/29902Medical Research Council G0601134Medical Research Council G0700091Medical Research Council G0800318Medical Research Council MR/J000841/1Medical Research Council MR/K002406/1
6 · The paper itself

Abstract

aimsThe contribution of blood flow to angiogenesis is incompletely understood. We examined the effect of blood flow on Notch signalling in the vasculature of zebrafish embryos, and whether blood flow regulates angiogenesis in zebrafish with constitutively up-regulated hypoxic signalling. METHODS AND

resultsDeveloping zebrafish (Danio rerio) embryos survive via diffusion in the absence of circulation induced by knockdown of cardiac troponin T2 or chemical cardiac cessation. The absence of blood flow increased vascular Notch signalling in 48 h post-fertilization old embryos via up-regulation of the Notch ligand dll4. Despite this, patterning of the intersegmental vessels is not affected by absent blood flow. We therefore examined homozygous vhl mutant zebrafish that have constitutively up-regulated hypoxic signalling. These display excessive and aberrant angiogenesis from 72 h post-fertilization, with significantly increased endothelial number, vessel diameter, and length. The absence of blood flow abolished these effects, though normal vessel patterning was preserved.

conclusionWe show that blood flow suppresses vascular Notch signalling via down-regulation of dll4. We have also shown that blood flow is required for angiogenesis in response to hypoxic signalling but is not required for normal vessel patterning. These data indicate important differences in hypoxia-driven vs. developmental angiogenesis.

Indexed as

Neovascularization, PhysiologicAnimalsBlood CirculationDiacetylHypoxiaIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptors, NotchSignal TransductionTumor Suppressor ProteinsVascular Endothelial Growth Factor Receptor-2ZebrafishZebrafish Proteinsdelta proteinDiacetyldiacetylmonoximeIntracellular Signaling Peptides and ProteinsMembrane ProteinsReceptors, NotchTumor Suppressor ProteinsVascular Endothelial Growth Factor Receptor-2Vhl protein, zebrafishZebrafish ProteinsAngio-/arteriogenesisAngiogenesisBlood flowNotchZebrafish

Identifiers

PMID23812297
PMCPMC3797625
OpenAlexW2109340777

What OpenQuestion holds

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LicenceCC BY-NC
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.