Evidence map›Paper›PMID 28656980›Full record

ArticleNature communications2017

Neurovascular EGFL7 regulates adult neurogenesis in the subventricular zone and thereby affects olfactory perception.

Frank Bicker, Verica Vasic, Guilherme Horta, Felipe Ortega, Hendrik Nolte, Atria Kavyanifar, Stefanie Keller, Nevenka Dudvarski Stankovic, Patrick N Harter, Rui Benedito and 9 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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

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  11. Understanding neural stem cell regulationRegenerative medicine · 2021
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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

19 authors at 7 institutions in 3 countries.

Frank BickerMolecular Signal Transduction Laboratories, Institute for Microscopic Anatomy and Neurobiology, Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Verica VasicMolecular Signal Transduction Laboratories, Institute for Microscopic Anatomy and Neurobiology, Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Guilherme HortaMolecular Signal Transduction Laboratories, Institute for Microscopic Anatomy and Neurobiology, Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Felipe OrtegaFocus Program Translational Neuroscience (FTN), Rhine Main Neuroscience Network (rmn2), Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Hendrik NolteInstitute for Genetics and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD) and Center for Molecular Medicine (CMMC), University of Cologne, Joseph-Stelzmann Straße 26, 50931 Cologne, Germany.
Atria KavyanifarMolecular Signal Transduction Laboratories, Institute for Microscopic Anatomy and Neurobiology, Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Stefanie KellerMolecular Signal Transduction Laboratories, Institute for Microscopic Anatomy and Neurobiology, Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Nevenka Dudvarski StankovicMolecular Signal Transduction Laboratories, Institute for Microscopic Anatomy and Neurobiology, Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Patrick N HarterEdinger-Institute (Neurological Institute), Goethe-University, School of Medicine, Heinrich-Hoffmann-Str. 7, 60528 Frankfurt am Main, Germany.
Rui BeneditoMolecular Genetics of Angiogenesis Laboratory, Centro Nacional de Investigaciones Cardiovasculares, Melchor Fernández Almagro 3, 28029 Madrid, Spain.
Beat LutzFocus Program Translational Neuroscience (FTN), Rhine Main Neuroscience Network (rmn2), Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Tobias BäuerlePreclinical Imaging Platform Erlangen, Institute of Radiology, University Medical Center Erlangen, Palmsanlage 5, 91054 Erlangen, Germany.
Jens HartwigInstitute for Molecular Biology, Johannes Gutenberg University, Ackermannweg 4, 55128 Mainz, Germany.
Jan BaumgartMolecular Signal Transduction Laboratories, Institute for Microscopic Anatomy and Neurobiology, Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Marcus KrügerInstitute for Genetics and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD) and Center for Molecular Medicine (CMMC), University of Cologne, Joseph-Stelzmann Straße 26, 50931 Cologne, Germany.
Konstantin RadyushkinMolecular Signal Transduction Laboratories, Institute for Microscopic Anatomy and Neurobiology, Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Lavinia AlberiSwiss Integrative Center for Human Health SA, Passage du Cardinal 13B, CH-1700 Fribourg, Switzerland.
Benedikt BerningerFocus Program Translational Neuroscience (FTN), Rhine Main Neuroscience Network (rmn2), Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.ORCID 0000-0003-2652-2782
Mirko H H SchmidtMolecular Signal Transduction Laboratories, Institute for Microscopic Anatomy and Neurobiology, Johannes Gutenberg University, School of Medicine, Langenbeckstraße 1, 55131 Mainz, Germany.
Johannes Gutenberg University Mainz · DEUniversity of Cologne · DEGoethe University Frankfurt · DESpanish National Centre for Cardiovascular Research · ESUniversidad Complutense de Madrid · ESUniversitätsklinikum Erlangen · DEUniversity of Fribourg · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adult neural stem cells reside in a specialized niche in the subventricular zone (SVZ). Throughout life they give rise to adult-born neurons in the olfactory bulb (OB), thus contributing to neural plasticity and pattern discrimination. Here, we show that the neurovascular protein EGFL7 is secreted by endothelial cells and neural stem cells (NSCs) of the SVZ to shape the vascular stem-cell niche. Loss of EGFL7 causes an accumulation of activated NSCs, which display enhanced activity and re-entry into the cell cycle. EGFL7 pushes activated NSCs towards quiescence and neuronal progeny towards differentiation. This is achieved by promoting Dll4-induced Notch signalling at the blood vessel-stem cell interface. Fewer inhibitory neurons form in the OB of EGFL7-knockout mice, which increases the absolute signal conducted from the mitral cell layer of the OB but decreases neuronal network synchronicity. Consequently, EGFL7-knockout mice display severe physiological defects in olfactory behaviour and perception.

Indexed as

NeurogenesisOlfactory PerceptionAdult Stem CellsAnimalsCalcium-Binding ProteinsCell CycleEGF Family of ProteinsLateral VentriclesMaleMiceMice, Inbred C57BLMice, KnockoutNeural Stem CellsNeuronal PlasticityProteinsSignal TransductionCalcium-Binding ProteinsEGF Family of ProteinsEgfl7 protein, mouseProteins

Identifiers

PMID28656980
PMCPMC5493759
OpenAlexW2730378541

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.