Evidence map›Paper›PMID 31748531›Full record

ArticleNature communications2019

Integrin-linked kinase controls retinal angiogenesis and is linked to Wnt signaling and exudative vitreoretinopathy.

Hongryeol Park, Hiroyuki Yamamoto, Lucas Mohn, Lea Ambühl, Kenichi Kanai, Inga Schmidt, Kee-Pyo Kim, Alessia Fraccaroli, Silke Feil, Harald J Junge and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. 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
6.1field-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

50 citing papers in PubMed, 84 citations in OpenAlex.

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  11. EndothelialFrontiers in cell and developmental biology · 2025
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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

13 authors at 6 institutions in 4 countries.

Hongryeol ParkMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, D-48149, Münster, Germany.
Hiroyuki YamamotoMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, D-48149, Münster, Germany.ORCID http://orcid.org/0000-0003-4742-7653
Lucas MohnInstitute of Medical Molecular Genetics, University of Zurich, CH-8952, Schlieren, Switzerland.
Lea AmbühlInstitute of Medical Molecular Genetics, University of Zurich, CH-8952, Schlieren, Switzerland.
Kenichi KanaiMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, D-48149, Münster, Germany.ORCID http://orcid.org/0000-0002-7758-5516
Inga SchmidtMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, D-48149, Münster, Germany.
Kee-Pyo KimMax Planck Institute for Molecular Biomedicine, Department of Cell and Developmental Biology, D-48149, Münster, Germany.ORCID http://orcid.org/0000-0002-8666-8444
Alessia FraccaroliWalter-Brendel-Centre of Experimental Medicine, University Hospital, LMU Munich, D-81377, Munich, Germany.
Silke FeilInstitute of Medical Molecular Genetics, University of Zurich, CH-8952, Schlieren, Switzerland.
Harald J JungeDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, CO, 80302, USA.ORCID http://orcid.org/0000-0003-2458-6010
Eloi MontanezWalter-Brendel-Centre of Experimental Medicine, University Hospital, LMU Munich, D-81377, Munich, Germany.ORCID http://orcid.org/0000-0003-4059-5056
Wolfgang BergerInstitute of Medical Molecular Genetics, University of Zurich, CH-8952, Schlieren, Switzerland. berger@medmolgen.uzh.ch.
Ralf H AdamsMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, D-48149, Münster, Germany. ralf.adams@mpi-muenster.mpg.de.ORCID http://orcid.org/0000-0003-3031-7677
University of Münster · DEUniversity of Zurich · CHInstitut d'Investigació Biomédica de Bellvitge · ESLMU Klinikum · DEMax Planck Institute for Molecular Biomedicine · DEUniversity of Colorado Boulder · US

Funding

Norrin Signaling in the Retina: Regulation of the Blood-Retina BarrierR01EY024261 · NEI · UNIVERSITY OF MINNESOTA · PI Harald Junge · 2014 to 2026
$4.7M
NEI NIH HHS R01 EY024261
6 · The paper itself

Abstract

Familial exudative vitreoretinopathy (FEVR) is a human disease characterized by defective retinal angiogenesis and associated complications that can result in vision loss. Defective Wnt/β-catenin signaling is an established cause of FEVR, whereas other molecular alterations contributing to the disease remain insufficiently understood. Here, we show that integrin-linked kinase (ILK), a mediator of cell-matrix interactions, is indispensable for retinal angiogenesis. Inactivation of the murine Ilk gene in postnatal endothelial cells results in sprouting defects, reduced endothelial proliferation and disruption of the blood-retina barrier, resembling phenotypes seen in established mouse models of FEVR. Retinal vascularization defects are phenocopied by inducible inactivation of the gene for α-parvin (Parva), an interactor of ILK. Screening genomic DNA samples from exudative vitreoretinopathy patients identifies three distinct mutations in human ILK, which compromise the function of the gene product in vitro. Together, our data suggest that defective cell-matrix interactions are linked to Wnt signaling and FEVR.

Indexed as

AnimalsBlood-Retinal BarrierEndothelial CellsFamilial Exudative VitreoretinopathiesFemaleHumansHuman Umbilical Vein Endothelial CellsMaleMiceMicrofilament ProteinsNeovascularization, PhysiologicPhenotypeProtein Serine-Threonine KinasesRetinal VesselsScaffold Protein ILKWnt Signaling PathwayMicrofilament ProteinsParva protein, mouseProtein Serine-Threonine KinasesScaffold Protein ILK

Identifiers

PMID31748531
PMCPMC6868140
OpenAlexW2989943253

What OpenQuestion holds

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LicenceCC BY
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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.