Evidence map›Paper›PMID 16314530›Full record

ArticleMolecular and cellular biology2005

Evidence for high-capacity bidirectional glucose transport across the endoplasmic reticulum membrane by genetically encoded fluorescence resonance energy transfer nanosensors.

Marcus Fehr, Hitomi Takanaga, David W Ehrhardt, Wolf B Frommer

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

46 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Glucose Transport and Transporters in the Endomembranes.International journal of molecular sciences · 2019
    Review
  9. Article
  10. Article
  11. Occludin regulates glucose uptake and ATP production in pericytes by influencing AMP-activated protein kinase activity.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2018
    Article
  12. Exploring cells with targeted biosensors.The Journal of general physiology · 2017
    Review
  13. Article
  14. Article
  15. Article
  16. Glucose transport machinery reconstituted in cell models.Chemical communications (Cambridge, England) · 2015
    Article
  17. Article
  18. FIBS-enabled noninvasive metabolic profiling.Journal of visualized experiments : JoVE · 2014
    Article
  19. Article
  20. Impact of L-FABP and glucose on polyunsaturated fatty acid induction of PPARα-regulated β-oxidative enzymes.American journal of physiology. Gastrointestinal and liver physiology · 2013
    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 1 institution in 1 country.

Marcus FehrCarnegie Institution, Stanford, CA 94305, USA.
Hitomi Takanaga
David W Ehrhardt
Wolf B Frommer
Carnegie Institution for Science · US

Funding

Oscilloscopes Spatio-Temporal Metabolomics (RMI)R33DK070272 · NIDDK · DUKE UNIVERSITY · PI YORK, JOHN D. · 2004 to 2006
$5.5M
NIDDK NIH HHS R33 DK070272NIDDK NIH HHS R33DK070272
6 · The paper itself

Abstract

Glucose release from hepatocytes is important for maintenance of blood glucose levels. Glucose-6-phosphate phosphatase, catalyzing the final metabolic step of gluconeogenesis, faces the endoplasmic reticulum (ER) lumen. Thus, glucose produced in the ER has to be either exported from the ER into the cytosol before release into circulation or exported directly by a vesicular pathway. To measure ER transport of glucose, fluorescence resonance energy transfer-based nanosensors were targeted to the cytosol or the ER lumen of HepG2 cells. During perfusion with 5 mM glucose, cytosolic levels were maintained at approximately 80% of the external supply, indicating that plasma membrane transport exceeded the rate of glucose phosphorylation. Glucose levels and kinetics inside the ER were indistinguishable from cytosolic levels, suggesting rapid bidirectional glucose transport across the ER membrane. A dynamic model incorporating rapid bidirectional ER transport yields a very good fit with the observed kinetics. Plasma membrane and ER membrane glucose transport differed regarding sensitivity to cytochalasin B and showed different relative kinetics for galactose uptake and release, suggesting catalysis by distinct activities at the two membranes. The presence of a high-capacity glucose transport system on the ER membrane is consistent with the hypothesis that glucose export from hepatocytes occurs via the cytosol by a yet-to-be-identified set of proteins.

Indexed as

Biosensing TechniquesFluorescence Resonance Energy TransferBiological TransportCell MembraneCytochalasin BCytosolEndoplasmic ReticulumGlucoseGlucose Transport Proteins, FacilitativeHepatocytesHumansIntracellular MembranesNanotechnologyCytochalasin BGlucoseGlucose Transport Proteins, Facilitative

Identifiers

PMID16314530
PMCPMC1316956
OpenAlexW2168968107

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.