Evidence map›Paper›PMID 31175156›Full record

ReviewThe Journal of biological chemistry2019

Thirty sweet years of GLUT4.

Amira Klip, Timothy E McGraw, David E James

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 178 papers.

0numbers the graph read from it
0cells of the map it votes in
178citing papers in PubMed
15.9field-weighted citation impact, top 1% 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

178 citing papers in PubMed, 351 citations in OpenAlex.

  1. Trial
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  8. Review
  9. A two-step mechanism for sugar translocation.Nature structural & molecular biology · 2026
    Article
  10. Article
  11. Article
  12. Review
  13. DietaryAnimal nutrition (Zhongguo xu mu shou yi xue hui) · 2026
    Article
  14. CD36 and Its Role in Obesity.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2026
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

118 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

3 authors at 3 institutions in 3 countries.

Amira KlipCell Biology Program, Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada amira@sickkids.ca.ORCID 0000-0001-7906-0302
Timothy E McGrawDepartment of Biochemistry, Weill Medical College of Cornell University, New York, New York 10065 temcgraw@med.cornell.edu.
David E JamesCharles Perkins Centre, School of Life and Environmental Sciences, Sydney Medical School, University of Sydney, Camperdown, New South Wales 2050, Australia david.james@sydney.edu.au.ORCID 0000-0001-5946-5257
Cornell University · USHospital for Sick Children · CAThe University of Sydney · AU

Funding

Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
NIDDK NIH HHS P30 DK020541
6 · The paper itself

Abstract

A pivotal metabolic function of insulin is the stimulation of glucose uptake into muscle and adipose tissues. The discovery of the insulin-responsive glucose transporter type 4 (GLUT4) protein in 1988 inspired its molecular cloning in the following year. It also spurred numerous cellular mechanistic studies laying the foundations for how insulin regulates glucose uptake by muscle and fat cells. Here, we reflect on the importance of the GLUT4 discovery and chronicle additional key findings made in the past 30 years. That exocytosis of a multispanning membrane protein regulates cellular glucose transport illuminated a novel adaptation of the secretory pathway, which is to transiently modulate the protein composition of the cellular plasma membrane. GLUT4 controls glucose transport into fat and muscle tissues in response to insulin and also into muscle during exercise. Thus, investigation of regulated GLUT4 trafficking provides a major means by which to map the essential signaling components that transmit the effects of insulin and exercise. Manipulation of the expression of GLUT4 or GLUT4-regulating molecules in mice has revealed the impact of glucose uptake on whole-body metabolism. Remaining gaps in our understanding of GLUT4 function and regulation are highlighted here, along with opportunities for future discoveries and for the development of therapeutic approaches to manage metabolic disease.

Indexed as

AnimalsBiological TransportCloning, MolecularGlucoseGlucose Transporter Type 4HumansInsulinInsulin ResistanceSignal TransductionGlucoseGlucose Transporter Type 4Insulindiabetesexerciseglucose metabolismglucose transportGLUT4 storage vesicle (GSV)insulinmetabolic syndromesignal transductionsolute carrier family 2 member 4 (SLC2A4)vesicle traffic

Identifiers

PMID31175156
PMCPMC6663870
OpenAlexW2964989731

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.