Evidence map›Paper›PMID 32483144›Full record

ArticleNature communications2020

Specific fibroblast subpopulations and neuronal structures provide local sources of Vegfc-processing components during zebrafish lymphangiogenesis.

Guangxia Wang, Lars Muhl, Yvonne Padberg, Laura Dupont, Josi Peterson-Maduro, Martin Stehling, Ferdinand le Noble, Alain Colige, Christer Betsholtz, Stefan Schulte-Merker and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 83 citations in OpenAlex.

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  18. Endothelial cell transitions in zebrafish vascular development.Development, growth & differentiation · 2024
    Review
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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 7 institutions in 5 countries.

Guangxia WangInstitute for Cardiovascular Organogenesis and Regeneration, WWU Münster, Münster, Germany.ORCID http://orcid.org/0000-0003-4827-6498
Lars MuhlIntegrated Cardio Metabolic Centre, Department of Medicine, Karolinska Institutet, Huddinge, Sweden.ORCID http://orcid.org/0000-0003-0952-0507
Yvonne PadbergInstitute for Cardiovascular Organogenesis and Regeneration, WWU Münster, Münster, Germany.ORCID http://orcid.org/0000-0001-5076-826X
Laura DupontLaboratory of Connective Tissue Biology, GIGA, University of Liège, Liege, Belgium.
Josi Peterson-MaduroHubrecht Institute-KNAW & UMC Utrecht, Utrecht, The Netherlands.
Martin StehlingFlow Cytometry Unit, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Ferdinand le NobleDepartment of Cell and Developmental Biology, Zoological Institute and Institute of Biological and Chemical Systems, Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany.
Alain ColigeLaboratory of Connective Tissue Biology, GIGA, University of Liège, Liege, Belgium.
Christer BetsholtzIntegrated Cardio Metabolic Centre, Department of Medicine, Karolinska Institutet, Huddinge, Sweden.
Stefan Schulte-MerkerInstitute for Cardiovascular Organogenesis and Regeneration, WWU Münster, Münster, Germany. schultes@ukmuenster.de.ORCID http://orcid.org/0000-0003-3617-8807
Andreas van ImpelInstitute for Cardiovascular Organogenesis and Regeneration, WWU Münster, Münster, Germany. vanimpel@uni-muenster.de.ORCID http://orcid.org/0000-0002-4737-3547
University of Münster · DEUniversity of Liège · BEKarlsruhe Institute of Technology · DEKarolinska Institutet · SEMax Planck Institute for Molecular Biomedicine · DEUniversity Medical Center Utrecht · NLUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteolytical processing of the growth factor VEGFC through the concerted activity of CCBE1 and ADAMTS3 is required for lymphatic development to occur. How these factors act together in time and space, and which cell types produce these factors is not understood. Here we assess the function of Adamts3 and the related protease Adamts14 during zebrafish lymphangiogenesis and show both proteins to be able to process Vegfc. Only the simultaneous loss of both protein functions results in lymphatic defects identical to vegfc loss-of-function situations. Cell transplantation experiments demonstrate neuronal structures and/or fibroblasts to constitute cellular sources not only for both proteases but also for Ccbe1 and Vegfc. We further show that this locally restricted Vegfc maturation is needed to trigger normal lymphatic sprouting and directional migration. Our data provide a single-cell resolution model for establishing secretion and processing hubs for Vegfc during developmental lymphangiogenesis.

Indexed as

ADAMTS ProteinsAnimalsAnimals, Genetically ModifiedFibroblastsGene Expression Regulation, DevelopmentalHEK293 CellsHumansLymphangiogenesisLymphatic VesselsMicroscopy, ConfocalNeuronsProcollagen N-EndopeptidaseVascular Endothelial Growth Factor CZebrafishZebrafish ProteinsADAMTS ProteinsProcollagen N-EndopeptidaseVascular Endothelial Growth Factor CZebrafish Proteins

Identifiers

PMID32483144
PMCPMC7264274
OpenAlexW3031690692

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.