Evidence map›Paper›PMID 28071661›Full record

ArticleNature communications2017

Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization.

Raphael Wild, Alina Klems, Masanari Takamiya, Yuya Hayashi, Uwe Strähle, Koji Ando, Naoki Mochizuki, Andreas van Impel, Stefan Schulte-Merker, Janna Krueger and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.8field-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

42 citing papers in PubMed, 75 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

12 authors at 5 institutions in 4 countries.

Raphael WildDepartment of Cell and Developmental Biology, Institute of Zoology (ZOO) Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, 76131 Karlsruhe, Germany.
Alina KlemsDepartment of Cell and Developmental Biology, Institute of Zoology (ZOO) Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, 76131 Karlsruhe, Germany.
Masanari TakamiyaInstitute for Toxicology and Genetics (ITG), Karlsruhe Institute of Technology (KIT), PO Box 3640, 76021 Karlsruhe, Germany.
Yuya HayashiInstitute for Toxicology and Genetics (ITG), Karlsruhe Institute of Technology (KIT), PO Box 3640, 76021 Karlsruhe, Germany.
Uwe SträhleInstitute for Toxicology and Genetics (ITG), Karlsruhe Institute of Technology (KIT), PO Box 3640, 76021 Karlsruhe, Germany.
Koji AndoDepartment of Cell Biology, National Cerebral and Cardiovascular Research Institute, 5-7-1 Fujisirodai, Suita, Osaka 565-8565, Japan.
Naoki MochizukiDepartment of Cell Biology, National Cerebral and Cardiovascular Research Institute, 5-7-1 Fujisirodai, Suita, Osaka 565-8565, Japan.
Andreas van ImpelInstitute for Cardiovascular Organogenesis and Regeneration, Faculty of Medicine, University of Münster, Mendelstr. 7, 48149 Münster, Germany.
Stefan Schulte-MerkerInstitute for Cardiovascular Organogenesis and Regeneration, Faculty of Medicine, University of Münster, Mendelstr. 7, 48149 Münster, Germany.
Janna KruegerDepartment of Translational Oncology, Biological Sciences Platform, Sunnybrook Research Institute, 2075 Bayview Ave., M4N 3M5 Toronto, Canada.
Laetitia PreauDepartment of Cell and Developmental Biology, Institute of Zoology (ZOO) Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, 76131 Karlsruhe, Germany.
Ferdinand le NobleDepartment of Cell and Developmental Biology, Institute of Zoology (ZOO) Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 4, 76131 Karlsruhe, Germany.
Karlsruhe Institute of Technology · DEUniversity of Münster · DECardiovascular Institute Hospital · JPNational Cerebral and Cardiovascular Center · JPSunnybrook Health Science Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Formation of organ-specific vasculatures requires cross-talk between developing tissue and specialized endothelial cells. Here we show how developing zebrafish spinal cord neurons coordinate vessel growth through balancing of neuron-derived Vegfaa, with neuronal sFlt1 restricting Vegfaa-Kdrl mediated angiogenesis at the neurovascular interface. Neuron-specific loss of flt1 or increased neuronal vegfaa expression promotes angiogenesis and peri-neural tube vascular network formation. Combining loss of neuronal flt1 with gain of vegfaa promotes sprout invasion into the neural tube. On loss of neuronal flt1, ectopic sprouts emanate from veins involving special angiogenic cell behaviours including nuclear positioning and a molecular signature distinct from primary arterial or secondary venous sprouting. Manipulation of arteriovenous identity or Notch signalling established that ectopic sprouting in flt1 mutants requires venous endothelium. Conceptually, our data suggest that spinal cord vascularization proceeds from veins involving two-tiered regulation of neuronal sFlt1 and Vegfaa via a novel sprouting mode.

Indexed as

AnimalsAnimals, Genetically ModifiedBiomarkersEmbryo, NonmammalianEndothelial CellsGene Expression Regulation, DevelopmentalMutationNeovascularization, PhysiologicNeuronsReceptors, NotchSpinal CordVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1VeinsZebrafish ProteinsBiomarkersFLT1 protein, zebrafishReceptors, NotchVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1Vegfaa protein, zebrafishZebrafish Proteins

Identifiers

PMID28071661
PMCPMC5234075
OpenAlexW2571141755

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.