Evidence map›Paper›PMID 26071524›Full record

ArticleJournal of cell science2015

Alternative routes to the cell surface underpin insulin-regulated membrane trafficking of GLUT4.

Dimitrios Kioumourtzoglou, Paul R Pryor, Gwyn W Gould, Nia J Bryant

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 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
0.6field-weighted citation impact, top 33% 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, 29 citations in OpenAlex.

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  16. InducibleThe Journal of biological chemistry · 2019
    Article
  17. Review
  18. Internalization of the Active Subunit of theFrontiers in cellular and infection microbiology · 2017
    Article
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

4 authors at 3 institutions in 1 country.

Dimitrios KioumourtzoglouInstitute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, G12 8QQ, UK Department of Biology, University of York, York YO10 5DD, UK.
Paul R PryorDepartment of Biology, University of York, York YO10 5DD, UK Centre for Immunology and Infection, Hull York Medical School, University of York, York YO10 5DD, UK.
Gwyn W GouldInstitute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, G12 8QQ, UK.
Nia J BryantInstitute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, G12 8QQ, UK Department of Biology, University of York, York YO10 5DD, UK gwyn.gould@glasgow.ac.uk nia.bryant@york.ac.uk.
University of Glasgow · GBHull York Medical School · GBUniversity of York · GB

Funding

Biotechnology and Biological Sciences Research Council BB/F016735/1Diabetes UK 11/0004289
6 · The paper itself

Abstract

Insulin-stimulated delivery of glucose transporters (GLUT4, also known as SLC2A4) from specialized intracellular GLUT4 storage vesicles (GSVs) to the surface of fat and muscle cells is central to whole-body glucose regulation. This translocation and subsequent internalization of GLUT4 back into intracellular stores transits through numerous small membrane-bound compartments (internal GLUT4-containing vesicles; IGVs) including GSVs, but the function of these different compartments is not clear. Cellugyrin (also known as synaptogyrin-2) and sortilin define distinct populations of IGV; sortilin-positive IGVs represent GSVs, but the function of cellugyrin-containing IGVs is unknown. Here, we demonstrate a role for cellugyrin in intracellular sequestration of GLUT4 in HeLa cells and have used a proximity ligation assay to follow changes in pairwise associations between cellugyrin, sortilin, GLUT4 and membrane trafficking machinery following insulin-stimulation of 3T3-L1 adipoctyes. Our data suggest that insulin stimulates traffic from cellugyrin-containing to sortilin-containing membranes, and that cellugyrin-containing IGVs provide an insulin-sensitive reservoir to replenish GSVs following insulin-stimulated exocytosis of GLUT4. Furthermore, our data support the existence of a pathway from cellugyrin-containing membranes to the surface of 3T3-L1 adipocytes that bypasses GSVs under basal conditions, and that insulin diverts traffic away from this into GSVs.

Indexed as

3T3-L1 CellsAdaptor Proteins, Vesicular TransportAnimalsCell MembraneExocytosisGlucose Transporter Type 4InsulinMiceProtein TransportSecretory VesiclesSortilinSynaptogyrinsAdaptor Proteins, Vesicular TransportGlucose Transporter Type 4InsulinSlc2a4 protein, mouseSortilinSynaptogyrinsEndosomeGyrinMembrane traffic

Identifiers

PMID26071524
PMCPMC4510850
OpenAlexW1955793736

What Socratic 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 Socratic graph.