Evidence map›Paper›PMID 33268383›Full record

ArticleThe Journal of biological chemistry

Lactate fluxes mediated by the monocarboxylate transporter-1 are key determinants of the metabolic activity of beige adipocytes.

Damien Lagarde, Yannick Jeanson, Corinne Barreau, Cedric Moro, Lindsay Peyriga, Edern Cahoreau, Christophe Guissard, Emmanuelle Arnaud, Anne Galinier, Anne-Karine Bouzier-Sore and 7 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

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  14. Lactate shuttling drives the browning of white adipose tissue after burn.American journal of physiology. Endocrinology and metabolism · 2023
    Article
  15. Article
  16. Review
  17. Role of histone lactylation interference RNA mFrontiers in cell and developmental biology · 2023
    Review
  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

17 authors at 4 institutions in 3 countries.

Damien LagardeSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France.
Yannick JeansonSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France.
Corinne BarreauSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France.
Cedric MoroInstitute of Metabolic and Cardiovascular Diseases, INSERM UMR1048, Paul Sabatier University, Toulouse, France.
Lindsay PeyrigaToulouse Biotechnology Institute TBI - INSA de Toulouse INSA/CNRS 5504 - UMR INSA/INRA 7924, Toulouse, France; MetaboHUB-MetaToul, National Infrastructure of Metabolomics and Fluxomics, Toulouse, France.
Edern CahoreauToulouse Biotechnology Institute TBI - INSA de Toulouse INSA/CNRS 5504 - UMR INSA/INRA 7924, Toulouse, France; MetaboHUB-MetaToul, National Infrastructure of Metabolomics and Fluxomics, Toulouse, France.
Christophe GuissardSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France.
Emmanuelle ArnaudSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France.
Anne GalinierSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France; Institut Fédératif de Biologie, CHU Purpan, Toulouse, France.
Anne-Karine Bouzier-SoreUniversité de Bordeaux, CNRS, CRMSB, UMR 5536, Bordeaux, France.
Luc PellerinINSERM U1082, Université de Poitiers, Poitiers Cedex, France.
Edward T ChouchaniDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA; Department of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Luc PénicaudSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France.
Isabelle AderSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France.
Jean-Charles PortaisSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France; Toulouse Biotechnology Institute TBI - INSA de Toulouse INSA/CNRS 5504 - UMR INSA/INRA 7924, Toulouse, France; MetaboHUB-MetaToul, National Infrastructure of Metabolomics and Fluxomics, Toulouse, France.
Louis CasteillaSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France.
Audrey CarrièreSTROMALab, Université de Toulouse, CNRS ERL5311, EFS, INP-ENVT, INSERM U1031, Université Paul Sabatier, Toulouse, France; Institut RESTORE, UMR 1301 INSERM, 5070 CNRS, Université Paul Sabatier, Toulouse, France. Electronic address: audrey.carriere-pazat@inserm.fr.
Centre National de la Recherche Scientifique · FRHarvard University · USInserm · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

Determining mechanisms of the succinate thermogenesis pathways on UCP1-dependent and UCP1-independent thermogenesisR01DK123095 · NIDDK · DANA-FARBER CANCER INST · PI Edward Thomas Chouchani · 2019 to 2026
$4.2M
NIDDK NIH HHS R01 DK123095
6 · The paper itself

Abstract

Activation of energy-dissipating brown/beige adipocytes represents an attractive therapeutic strategy against metabolic disorders. While lactate is known to induce beiging through the regulation of Ucp1 gene expression, the role of lactate transporters on beige adipocytes' ongoing metabolic activity remains poorly understood. To explore the function of the lactate-transporting monocarboxylate transporters (MCTs), we used a combination of primary cell culture studies,

Indexed as

Gene Expression RegulationAdipocytes, BeigeAnimalsLactic AcidMaleMesenchymal Stem CellsMiceMice, Inbred C57BLMonocarboxylate Transport Protein 1Monocarboxylic Acid TransportersSignal TransductionSymportersThermogenesisLactic AcidMonocarboxylate Transport Protein 1Monocarboxylic Acid TransportersSymportersbeige adipocytesglycolysislactate fluxesmonocarboxylate transportersuncoupling protein 1

Identifiers

PMID33268383
PMCPMC7949083
OpenAlexW3108972864

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.