Evidence map›Paper›PMID 11274399›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Restoration of insulin-sensitive glucose transporter (GLUT4) gene expression in muscle cells by the transcriptional coactivator PGC-1.

L F Michael, Z Wu, R B Cheatham, P Puigserver, G Adelmant, J J Lehman, D P Kelly, B M Spiegelman

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 268 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
268citing papers in PubMed, 3 pooled it
14.3field-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

268 citing papers in PubMed, 3 syntheses or guidelines pooled it, 655 citations in OpenAlex.

  1. Association between theFrontiers in physiology · 2025
    Pooled it
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  4. Trial
  5. Review
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  8. The Sirtuin Network: Linking NADDiabetes/metabolism research and reviews · 2026
    Review
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  11. Article
  12. The Role of Gene Therapy and RNA-Based Therapeutic Strategies in Diabetes.International journal of molecular sciences · 2025
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

208 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

8 authors at 3 institutions in 1 country.

L F MichaelDana-Farber Cancer Institute, Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Z Wu
R B Cheatham
P Puigserver
G Adelmant
J J Lehman
D P Kelly
B M Spiegelman
Dana-Farber Cancer Institute · USJoslin Diabetes Center · USHarvard University · US

Funding

PGC-1 AND NUCLEAR RECEPTORS IN ADAPTIVE THERMOGENESISR01DK054477 · NIDDK · DANA-FARBER CANCER INSTITUTE · PI SPIEGELMAN, BRUCE M. · 1998 to 2016
$7.0M
PGC-1 and Nuclear Receptors in Adaptive ThermogenesisR56DK054477 · NIDDK · DANA-FARBER CANCER INST · PI SPIEGELMAN, BRUCE M · 2006 to 2006
$395k
SIGNAL DISCRIMINATION BY CBPF32GM019680 · NIGMS · JOSLIN DIABETES CENTER · PI MICHAEL, LAURA F · 1998 to 2000
$21k
NIDDK NIH HHS DK54477NIDDK NIH HHS R01 DK054477NIDDK NIH HHS R56 DK054477NIGMS NIH HHS F32 GM019680NIGMS NIH HHS GM19680
6 · The paper itself

Abstract

Muscle tissue is the major site for insulin-stimulated glucose uptake in vivo, due primarily to the recruitment of the insulin-sensitive glucose transporter (GLUT4) to the plasma membrane. Surprisingly, virtually all cultured muscle cells express little or no GLUT4. We show here that adenovirus-mediated expression of the transcriptional coactivator PGC-1, which is expressed in muscle in vivo but is also deficient in cultured muscle cells, causes the total restoration of GLUT4 mRNA levels to those observed in vivo. This increased GLUT4 expression correlates with a 3-fold increase in glucose transport, although much of this protein is transported to the plasma membrane even in the absence of insulin. PGC-1 mediates this increased GLUT4 expression, in large part, by binding to and coactivating the muscle-selective transcription factor MEF2C. These data indicate that PGC-1 is a coactivator of MEF2C and can control the level of endogenous GLUT4 gene expression in muscle.

Indexed as

Muscle ProteinsAnimalsBiological TransportCells, CulturedGene ExpressionGlucoseGlucose Transporter Type 4InsulinMEF2 Transcription FactorsMiceMonosaccharide Transport ProteinsMuscle, SkeletalMyogenic Regulatory FactorsProtein Structure, TertiaryRatsTranscription FactorsGlucoseGlucose Transporter Type 4InsulinMef2c protein, mouseMEF2 Transcription FactorsMonosaccharide Transport ProteinsMuscle ProteinsMyogenic Regulatory Factorsperoxisome-proliferator-activated receptor-gamma coactivator-1Slc2a4 protein, mouseSlc2a4 protein, ratTranscription Factors

Identifiers

PMID11274399
PMCPMC31136
OpenAlexW2028026629

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.