Evidence map›Paper›PMID 38570531›Full record

ArticleNature communications2024

Eph-ephrin signaling couples endothelial cell sorting and arterial specification.

Jonas Stewen, Kai Kruse, Anca T Godoi-Filip, Zenia, Hyun-Woo Jeong, Susanne Adams, Frank Berkenfeld, Martin Stehling, Kristy Red-Horse, Ralf H Adams and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

23 citing papers in PubMed, 28 citations in OpenAlex.

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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 2 countries.

Jonas StewenDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.ORCID http://orcid.org/0000-0002-1155-3079
Kai KruseDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.ORCID http://orcid.org/0000-0002-7951-7357
Anca T Godoi-FilipDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.ORCID http://orcid.org/0009-0007-8508-8310
ZeniaDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.ORCID http://orcid.org/0009-0001-9751-1506
Hyun-Woo JeongDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.ORCID http://orcid.org/0000-0002-6976-6739
Susanne AdamsDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.
Frank BerkenfeldDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.
Martin StehlingFlow Cytometry Unit, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany.
Kristy Red-HorseDepartment of Biology, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0003-1541-601X
Ralf H AdamsDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany. ralf.adams@mpi-muenster.mpg.de.ORCID http://orcid.org/0000-0003-3031-7677
Mara E PitulescuDepartment of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, D-48149, Münster, Germany. mara.pitulescu@mpi-muenster.mpg.de.ORCID http://orcid.org/0000-0001-5322-8146
Max Planck Institute for Molecular Biomedicine · DEHoward Hughes Medical Institute · US

Funding

Mechanotransduction and transcriptional regulation during artery developmentR01HL128503 · NHLBI · STANFORD UNIVERSITY · PI Mary Red-Horse · 2015 to 2026
$5.8M
NHLBI NIH HHS R01 HL128503
6 · The paper itself

Abstract

Cell segregation allows the compartmentalization of cells with similar fates during morphogenesis, which can be enhanced by cell fate plasticity in response to local molecular and biomechanical cues. Endothelial tip cells in the growing retina, which lead vessel sprouts, give rise to arterial endothelial cells and thereby mediate arterial growth. Here, we have combined cell type-specific and inducible mouse genetics, flow experiments in vitro, single-cell RNA sequencing and biochemistry to show that the balance between ephrin-B2 and its receptor EphB4 is critical for arterial specification, cell sorting and arteriovenous patterning. At the molecular level, elevated ephrin-B2 function after loss of EphB4 enhances signaling responses by the Notch pathway, VEGF and the transcription factor Dach1, which is influenced by endothelial shear stress. Our findings reveal how Eph-ephrin interactions integrate cell segregation and arteriovenous specification in the vasculature, which has potential relevance for human vascular malformations caused by EPHB4 mutations.

Indexed as

Endothelial CellsEphrinsAnimalsArteriesCell SeparationEphrin-B2HumansMiceReceptor, EphB4Receptor Protein-Tyrosine KinasesEphrin-B2EphrinsReceptor, EphB4Receptor Protein-Tyrosine Kinases

Identifiers

PMID38570531
PMCPMC10991410
OpenAlexW4393902406

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.