Evidence map›Paper›PMID 26437238›Full record

ArticleNature communications2015

Stonin1 mediates endocytosis of the proteoglycan NG2 and regulates focal adhesion dynamics and cell motility.

Fabian Feutlinske, Marietta Browarski, Min-Chi Ku, Philipp Trnka, Sonia Waiczies, Thoralf Niendorf, William B Stallcup, Rainer Glass, Eberhard Krause, Tanja Maritzen

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

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  16. Clock Scan Protocol for Image Analysis: ImageJ Plugins.Journal of visualized experiments : JoVE · 2017
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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

10 authors at 4 institutions in 2 countries.

Fabian FeutlinskeLeibniz-Institut für Molekulare Pharmakologie (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Marietta BrowarskiLeibniz-Institut für Molekulare Pharmakologie (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Min-Chi KuBerlin Ultrahigh Field Facility (B.U.F.F.), Max-Delbrueck Center for Molecular Medicine, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Philipp TrnkaLeibniz-Institut für Molekulare Pharmakologie (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Sonia WaicziesBerlin Ultrahigh Field Facility (B.U.F.F.), Max-Delbrueck Center for Molecular Medicine, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Thoralf NiendorfBerlin Ultrahigh Field Facility (B.U.F.F.), Max-Delbrueck Center for Molecular Medicine, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
William B StallcupTumor Microenvironment and Metastasis Program, Cancer Center, Sanford-Burnham Medical Research Institute, 10901 North Torrey Pines Road, La Jolla, California 92037, USA.
Rainer GlassNeurosurgical Research, Clinic for Neurosurgery, Ludwig Maximilians University of Munich, Marchionistrasse 15, 81377 Munich, Germany.
Eberhard KrauseLeibniz-Institut für Molekulare Pharmakologie (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Tanja MaritzenLeibniz-Institut für Molekulare Pharmakologie (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany.
Leibniz-Forschungsinstitut für Molekulare Pharmakologie · DEMax Delbrück Center · DELudwig-Maximilians-Universität München · DESanford Burnham Prebys Medical Discovery Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular functions, ranging from focal adhesion (FA) dynamics and cell motility to tumour growth, are orchestrated by signals cells receive from outside via cell surface receptors. Signalling is fine-tuned by the exo-endocytic cycling of these receptors to control cellular responses such as FA dynamics, which determine cell motility. How precisely endocytosis regulates turnover of the various cell surface receptors remains unclear. Here we identify Stonin1, an endocytic adaptor of unknown function, as a regulator of FA dynamics and cell motility, and demonstrate that it facilitates the internalization of the oncogenic proteoglycan NG2, a co-receptor of integrins and platelet-derived growth factor receptor. Embryonic fibroblasts obtained from Stonin1-deficient mice display a marked surface accumulation of NG2, increased cellular signalling and defective FA disassembly as well as altered cellular motility. These data establish Stonin1 as a specific adaptor for the endocytosis of NG2 and as an important factor for FA dynamics and cell migration.

Indexed as

Adaptor Proteins, Vesicular TransportAnimalsAntigensCell MovementChondroitin Sulfate Proteoglycan 4Chromatography, LiquidEndocytosisFibroblastsFlow CytometryFluorescent Antibody TechniqueFocal AdhesionsHEK293 CellsHumansMembrane ProteinsMiceMice, KnockoutAdaptor Proteins, Vesicular TransportAntigensChondroitin Sulfate Proteoglycan 4Membrane ProteinsProteoglycansStonin1 protein, mouseTranscription Factors, General

Identifiers

PMID26437238
PMCPMC4600748
OpenAlexW2270807519

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.