Evidence map›Paper›PMID 21691894›Full record

ReviewPharmaceutical research2011

Quantitative glucose and ATP sensing in mammalian cells.

Dania C Liemburg-Apers, Hiromi Imamura, Marleen Forkink, Marco Nooteboom, Herman G Swarts, Roland Brock, Jan A M Smeitink, Peter H G M Willems, Werner J H Koopman

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Pharmaceutical research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
  2. Article
  3. Mitochondrial Dynamics and Insulin Secretion.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. A Non-Invasive Tool for Real-Time Measurement of Sulfate in Living Cells.International journal of molecular sciences · 2020
    Article
  11. Spatial heterogeneity in the mammalian liver.Nature reviews. Gastroenterology & hepatology · 2019
    Review
  12. Mitochondrial Morphofunction in Mammalian Cells.Antioxidants & redox signaling · 2019
    Review
  13. Article
  14. Review
  15. Article
  16. Synthesis of newBeilstein journal of organic chemistry · 2018
    Article
  17. Article
  18. Article
  19. Article
  20. Review
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

9 authors at 3 institutions in 2 countries.

Dania C Liemburg-ApersDepartment of Biochemistry (286) Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, P.O. Box 9101, NL-6500 HB, Nijmegen, The Netherlands.
Hiromi Imamura
Marleen Forkink
Marco Nooteboom
Herman G Swarts
Roland Brock
Jan A M Smeitink
Peter H G M Willems
Werner J H Koopman
Radboud University Nijmegen · NLRadboud University Medical Center · NLKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The functioning and survival of mammalian cells requires an active energy metabolism. Metabolic dysfunction plays an important role in many human diseases, including diabetes, cancer, inherited mitochondrial disorders, and metabolic syndrome. The monosaccharide glucose constitutes a key source of cellular energy. Following its import across the plasma membrane, glucose is converted into pyruvate by the glycolysis pathway. Pyruvate oxidation supplies substrates for the ATP-generating mitochondrial oxidative phosphorylation (OXPHOS) system. To gain cell-biochemical knowledge about the operation and regulation of the cellular energy metabolism in the healthy and diseased state, quantitative knowledge is required about (changes in) metabolite concentrations under (non) steady-state conditions. This information can, for instance, be used to construct more realistic in silico models of cell metabolism, which facilitates understanding the consequences of metabolic dysfunction as well as on- and off-target effects of mitochondrial drugs. Here we review the current state-of-the-art live-cell quantification of two key cellular metabolites, glucose and ATP, using protein-based sensors. The latter apply the principle of FRET (fluorescence resonance energy transfer) and allow measurements in different cell compartments by fluorescence microscopy. We further summarize the properties and applications of the FRET-based sensors, their calibration, pitfalls, and future perspectives.

Indexed as

Adenosine TriphosphateAnimalsBiosensing TechniquesCalibrationFluorescence Resonance Energy TransferGlucoseHumansMammalsMicroscopyAdenosine TriphosphateGlucose

Identifiers

PMID21691894
OpenAlexW2139417020

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.