Evidence map›Paper›PMID 28714968›Full record

ArticleNature cell biology2017

Dll4 and Notch signalling couples sprouting angiogenesis and artery formation.

Mara E Pitulescu, Inga Schmidt, Benedetto Daniele Giaimo, Tobiah Antoine, Frank Berkenfeld, Francesca Ferrante, Hongryeol Park, Manuel Ehling, Daniel Biljes, Susana F Rocha and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 273 papers.

0numbers the graph read from it
0cells of the map it votes in
273citing papers in PubMed
12.9field-weighted citation impact, top 1% 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

273 citing papers in PubMed, 391 citations in OpenAlex.

  1. Review
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  5. CD4Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  20. Zebrafish in Cardiovascular Disease Research: from Model to Application.International journal of biological sciences · 2026
    Review

213 more citing papers are in PubMed but not listed here.

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

16 authors at 5 institutions in 3 countries.

Mara E PitulescuMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, and University of Münster, Faculty of Medicine, Röntgenstrasse 20, D-48149 Münster, Germany.
Inga SchmidtMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, and University of Münster, Faculty of Medicine, Röntgenstrasse 20, D-48149 Münster, Germany.
Benedetto Daniele GiaimoInstitute of Biochemistry, University of Giessen, Friedrichstrasse 24, D-35392 Giessen, Germany.
Tobiah AntoineMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, and University of Münster, Faculty of Medicine, Röntgenstrasse 20, D-48149 Münster, Germany.
Frank BerkenfeldMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, and University of Münster, Faculty of Medicine, Röntgenstrasse 20, D-48149 Münster, Germany.
Francesca FerranteInstitute of Biochemistry, University of Giessen, Friedrichstrasse 24, D-35392 Giessen, Germany.
Hongryeol ParkMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, and University of Münster, Faculty of Medicine, Röntgenstrasse 20, D-48149 Münster, Germany.
Manuel EhlingMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, and University of Münster, Faculty of Medicine, Röntgenstrasse 20, D-48149 Münster, Germany.
Daniel BiljesMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, and University of Münster, Faculty of Medicine, Röntgenstrasse 20, D-48149 Münster, Germany.
Susana F RochaMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, and University of Münster, Faculty of Medicine, Röntgenstrasse 20, D-48149 Münster, Germany.
Urs H LangenMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, and University of Münster, Faculty of Medicine, Röntgenstrasse 20, D-48149 Münster, Germany.ORCID http://orcid.org/0000-0002-7412-276X
Martin StehlingMax Planck Institute for Molecular Biomedicine, Flow Cytometry Unit, Röntgenstrasse 20, D-48149 Münster, Germany.
Takashi NagasawaLaboratory of Stem Cell Biology and Developmental Immunology, Graduate School of Frontier Biosciences and Graduate School of Medicine, Osaka University, 1-3 Yamada-oka, Suita, Osaka 565-0871, Japan.
Napoleone FerraraUniversity of California San Diego Medical Center, 9500 Gilman Drive, La Jolla, California 92093, USA.
Tilman BorggrefeInstitute of Biochemistry, University of Giessen, Friedrichstrasse 24, D-35392 Giessen, Germany.
Ralf H AdamsMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, and University of Münster, Faculty of Medicine, Röntgenstrasse 20, D-48149 Münster, Germany.ORCID http://orcid.org/0000-0003-3031-7677
University of Münster · DEJustus-Liebig-Universität Gießen · DEMax Planck Institute for Molecular Biomedicine · DEThe University of Osaka · JPUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelial sprouting and proliferation are tightly coordinated processes mediating the formation of new blood vessels during physiological and pathological angiogenesis. Endothelial tip cells lead sprouts and are thought to suppress tip-like behaviour in adjacent stalk endothelial cells by activating Notch. Here, we show with genetic experiments in postnatal mice that the level of active Notch signalling is more important than the direct Dll4-mediated cell-cell communication between endothelial cells. We identify endothelial expression of VEGF-A and of the chemokine receptor CXCR4 as key processes controlling Notch-dependent vessel growth. Surprisingly, genetic experiments targeting endothelial tip cells in vivo reveal that they retain their function without Dll4 and are also not replaced by adjacent, Dll4-positive cells. Instead, activation of Notch directs tip-derived endothelial cells into developing arteries and thereby establishes that Dll4-Notch signalling couples sprouting angiogenesis and artery formation.

Indexed as

Neovascularization, PhysiologicAdaptor Proteins, Signal TransducingAnimalsCalcium-Binding ProteinsCell CommunicationCell DifferentiationCell LineageCell MovementCell ProliferationCells, CulturedEndothelial CellsFemaleGene Expression RegulationGenotypeIntracellular Signaling Peptides and ProteinsJagged-1 ProteinAdaptor Proteins, Signal TransducingCalcium-Binding ProteinsCXCR4 protein, mouseDLL4 protein, mouseIntracellular Signaling Peptides and ProteinsJag1 protein, mouseJagged-1 ProteinMembrane ProteinsNotch1 protein, mouseReceptor, Notch1Receptors, CXCR4Vascular Endothelial Growth Factor Avascular endothelial growth factor A, mouse

Identifiers

PMID28714968
OpenAlexW2734395509

What OpenQuestion holds

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Registered trials

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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.