Evidence map›Paper›PMID 12134080›Full record

ArticleMolecular biology of the cell2002

GLUT4 retention in adipocytes requires two intracellular insulin-regulated transport steps.

Anja Zeigerer, Michael A Lampson, Ola Karylowski, David D Sabatini, Milton Adesnik, Mindong Ren, Timothy E McGraw

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

76 citing papers in PubMed, 176 citations in OpenAlex.

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  10. Review
  11. Metabolic regulation through the endosomal system.Traffic (Copenhagen, Denmark) · 2019
    Review
  12. Thirty sweet years of GLUT4.The Journal of biological chemistry · 2019
    Review
  13. Article
  14. AMPA Receptor Trafficking for Postsynaptic Potentiation.Frontiers in cellular neuroscience · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

16 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Anja ZeigererDepartment of Biochemistry, Biophysics and Molecular Medicine, Weill Medical College of Cornell University, New York, New York 10021, USA.
Michael A Lampson
Ola Karylowski
David D Sabatini
Milton Adesnik
Mindong Ren
Timothy E McGraw
New York University · USCornell University · US

Funding

INSULIN REGULATED MEMBRANE TRAFFICKINGR01DK052852 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI MCGRAW, TIMOTHY E · 1997 to 2016
$6.1M
REGULATED ENDOCYTIC TRAFFIC IN FIBROBLASTSR01DK057689 · NIDDK · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI MCGRAW, TIMOTHY E · 2001 to 2004
$1.2M
Insulin Regulated Membrane TraffickingR56DK052852 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI MCGRAW, TIMOTHY E · 2017 to 2017
$254k
NIDDK NIH HHS DK-52852NIDDK NIH HHS DK-57689NIDDK NIH HHS R01 DK052852NIDDK NIH HHS R01 DK057689NIDDK NIH HHS R56 DK052852
6 · The paper itself

Abstract

Insulin regulates glucose uptake into fat and muscle by modulating the distribution of the GLUT4 glucose transporter between the surface and interior of cells. The GLUT4 trafficking pathway overlaps with the general endocytic recycling pathway, but the degree and functional significance of the overlap are not known. In this study of intact adipocytes, we demonstrate, by using a compartment-specific fluorescence-quenching assay, that GLUT4 is equally distributed between two intracellular pools: the transferrin receptor-containing endosomes and a specialized compartment that excludes the transferrin receptor. These pools of GLUT4 are in dynamic communication with one another and with the cell surface. Insulin-induced redistribution of GLUT4 to the surface requires mobilization of both pools. These data establish a role for the general endosomal system in the specialized, insulin-regulated trafficking of GLUT4. Trafficking through the general endosomal system is regulated by rab11. Herein, we show that rab11 is required for the transport of GLUT4 from endosomes to the specialized compartment and for the insulin-induced translocation to the cell surface, emphasizing the importance of the general endosomal pathway in the specialized trafficking of GLUT4. Based on these findings we propose a two-step model for GLUT4 trafficking in which the general endosomal recycling compartment plays a specialized role in the insulin-regulated traffic of GLUT4. This compartment-based model provides the framework for understanding insulin-regulated trafficking at a molecular level.

Indexed as

Muscle Proteins3T3 CellsAdipocytesAnimalsBiological TransportCytoplasmic VesiclesEndosomesFluorescent DyesGlucoseGlucose Transporter Type 4HumansInsulinMiceMonosaccharide Transport Proteinsrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsFluorescent DyesGlucoseGlucose Transporter Type 4InsulinMonosaccharide Transport ProteinsMuscle Proteinsrab11 GTP-Binding Proteinsrab GTP-Binding ProteinsReceptors, TransferrinRecombinant Fusion ProteinsSLC2A4 protein, humanSlc2a4 protein, mouseTransferrin

Identifiers

PMID12134080
PMCPMC117324
OpenAlexW2143339101

What OpenQuestion holds

Textmetadata
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.