Evidence map›Paper›PMID 26639784›Full record

ArticleScientific reports2015

GLUT3 and PKM2 regulate OCT4 expression and support the hypoxic culture of human embryonic stem cells.

David R Christensen, Philip C Calder, Franchesca D Houghton

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

32 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Review
  6. Article
  7. Glioblastoma Metabolism: Insights and Therapeutic Strategies.International journal of molecular sciences · 2023
    Review
  8. Metabolic control of induced pluripotency.Frontiers in cell and developmental biology · 2023
    Review
  9. Review
  10. Article
  11. The Role of Nitric Oxide in Stem Cell Biology.Antioxidants (Basel, Switzerland) · 2022
    Review
  12. Review
  13. Article
  14. Regulation of energy metabolism in human pluripotent stem cells.Cellular and molecular life sciences : CMLS · 2021
    Review
  15. Article
  16. 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

3 authors at 2 institutions in 1 country.

David R ChristensenCentre for Human Development, Stem Cells &Regeneration, Faculty of Medicine, University of Southampton, Southampton, SO16 6YD, UK.
Philip C CalderHuman Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, SO16 6YD, UK.
Franchesca D HoughtonCentre for Human Development, Stem Cells &Regeneration, Faculty of Medicine, University of Southampton, Southampton, SO16 6YD, UK.
University of Southampton · GBNIHR Southampton Biomedical Research Centre · GB

Funding

Medical Research Council G0701153Medical Research Council G1000406
6 · The paper itself

Abstract

Human embryonic stem cells (hESCs) have the capacity to differentiate into all cell types and thus have great potential for regenerative medicine. hESCs cultured at low oxygen tensions are more pluripotent and display an increased glycolytic rate but how this is regulated is unknown. This study therefore aimed to investigate the regulation of glucose metabolism in hESCs and whether this might impact OCT4 expression. In contrast to the glucose transporter GLUT1, GLUT3 was regulated by environmental oxygen and localised to hESC membranes. Silencing GLUT3 caused a reduction in glucose uptake and lactate production as well as OCT4 expression. GLUT3 and OCT4 expression were correlated suggesting that hESC self-renewal is regulated by the rate of glucose uptake. Surprisingly, PKM2, a rate limiting enzyme of glycolysis displayed a nuclear localisation in hESCs and silencing PKM2 did not alter glucose metabolism suggesting a role other than as a glycolytic enzyme. PKM2 expression was increased in hESCs cultured at 5% oxygen compared to 20% oxygen and silencing PKM2 reduced OCT4 expression highlighting a transcriptional role for PKM2 in hESCs. Together, these data demonstrate two separate mechanisms by which genes regulating glucose uptake and metabolism are involved in the hypoxic support of pluripotency in hESCs.

Indexed as

Carrier ProteinsCell HypoxiaCell MembraneCell NucleusCells, CulturedGene SilencingGlucoseGlucose Transporter Type 1Glucose Transporter Type 3Human Embryonic Stem CellsHumansLactic AcidMembrane ProteinsOctamer Transcription Factor-3OxygenProtein TransportCarrier ProteinsGlucoseGlucose Transporter Type 1Glucose Transporter Type 3Lactic AcidMembrane ProteinsOctamer Transcription Factor-3OxygenPOU5F1 protein, humanSLC2A1 protein, humanSLC2A3 protein, humanThyroid Hormone-Binding ProteinsThyroid Hormones

Identifiers

PMID26639784
PMCPMC4671001
OpenAlexW2235114745

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.