Evidence map›Paper›PMID 18577699›Full record

ReviewAmerican journal of physiology. Endocrinology and metabolism2008

The facilitative glucose transporter GLUT3: 20 years of distinction.

Ian A Simpson, Donard Dwyer, Daniela Malide, Kelle H Moley, Alexander Travis, Susan J Vannucci

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Endocrinology and metabolism, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 263 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
263citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 3% 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

263 citing papers in PubMed, 1 synthesis or guideline pooled it, 471 citations in OpenAlex.

  1. Pooled it
  2. [Molecular imaging and biology · 2021
    Trial
  3. Review
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  5. Review
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  7. Learning Shapes the Energy Cost of Neural Tasks.bioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. GLUT1 expression, lymphocyte distribution and CD3Journal of experimental & clinical cancer research : CR · 2026
    Article
  12. Article
  13. Article
  14. Loss ofLife science alliance · 2026
    Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

203 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

6 authors at 5 institutions in 1 country.

Ian A SimpsonDepartment of Neural and Behavioral Sciences, College of Medicine, Penn State University, 500 University Drive, Hershey, PA 17033, USA. ixs10@psu.edu
Donard Dwyer
Daniela Malide
Kelle H Moley
Alexander Travis
Susan J Vannucci
Cornell University · USLouisiana State University Health Sciences Center Shreveport · USNational Institutes of Health · USPennsylvania State University · USWashington University in St. Louis · US

Funding

Light Microscopy CoreZICHL006019 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI COMBS, CHRISTIAN · 2009 to 2025
$29.3M
Diabetes & Stroke: Impaired wound healing in the brain?R01DK075130 · NIDDK · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SIMPSON, IAN A · 2007 to 2011
$1.6M
IGF Induced Toxicity in Preimplantation EmbryosR01DK070351 · NIDDK · WASHINGTON UNIVERSITY · PI MOLEY, KELLE H · 2004 to 2007
$1.4M
ORGANIZATION AND FUNCTIONS OF LIPID RAFTS IN SPERMATOZOAR01HD045664 · NICHD · CORNELL UNIVERSITY ITHACA · PI TRAVIS, ALEXANDER J · 2004 to 2008
$1.3M
Blood-Brain Barrier Nutrient TransportR01NS041405 · NINDS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SIMPSON, IAN A · 2003 to 2006
$1.3M
Molecular Aspects of ImplantationR01HD040810 · NICHD · WASHINGTON UNIVERSITY · PI MOLEY, KELLE H · 2002 to 2006
$1.2M
NCRR NIH HHS RR 00188NICHD NIH HHS HD 040810NICHD NIH HHS HD 045664NIDDK NIH HHS DK 070351NIDDK NIH HHS DK 075130NINDS NIH HHS NS 041405
6 · The paper itself

Abstract

Glucose metabolism is vital to most mammalian cells, and the passage of glucose across cell membranes is facilitated by a family of integral membrane transporter proteins, the GLUTs. There are currently 14 members of the SLC2 family of GLUTs, several of which have been the focus of this series of reviews. The subject of the present review is GLUT3, which, as implied by its name, was the third glucose transporter to be cloned (Kayano T, Fukumoto H, Eddy RL, Fan YS, Byers MG, Shows TB, Bell GI. J Biol Chem 263: 15245-15248, 1988) and was originally designated as the neuronal GLUT. The overriding question that drove the early work on GLUT3 was why would neurons need a separate glucose transporter isoform? What is it about GLUT3 that specifically suits the needs of the highly metabolic and oxidative neuron with its high glucose demand? More recently, GLUT3 has been studied in other cell types with quite specific requirements for glucose, including sperm, preimplantation embryos, circulating white blood cells, and an array of carcinoma cell lines. The last are sufficiently varied and numerous to warrant a review of their own and will not be discussed here. However, for each of these cases, the same questions apply. Thus, the objective of this review is to discuss the properties and tissue and cellular localization of GLUT3 as well as the features of expression, function, and regulation that distinguish it from the rest of its family and make it uniquely suited as the mediator of glucose delivery to these specific cells.

Indexed as

AnimalsGlucoseGlucose Transporter Type 3HumansModels, MolecularNeuronsGlucoseGlucose Transporter Type 3

Identifiers

PMID18577699
PMCPMC2519757
OpenAlexW2109661060

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.