Evidence map›Paper›PMID 28270520›Full record

ArticleDiabetes2017

Functional Human Beige Adipocytes From Induced Pluripotent Stem Cells.

Anne-Claire Guénantin, Nolwenn Briand, Emilie Capel, Florent Dumont, Romain Morichon, Claire Provost, Francesca Stillitano, Dorota Jeziorowska, Jean-Pierre Siffroi, Roger J Hajjar and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 75 citations in OpenAlex.

  1. Pooled it
  2. A futile NaNature metabolism · 2026
    Article
  3. Review
  4. Thermogenesis is limited by cellular competence.Frontiers in cell and developmental biology · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Bioreactors, scaffolds and microcarriers andFrontiers in nutrition · 2023
    Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 4 countries.

Anne-Claire GuénantinSorbonne Universités, Université Pierre et Marie Curie, INSERM UMR_S938, Centre de Recherche Saint-Antoine, Institute of Cardiometabolism and Nutrition, Paris, France anne-claire.guenantin@inserm.fr nolwenn.briand@inserm.fr.
Nolwenn BriandSorbonne Universités, Université Pierre et Marie Curie, INSERM UMR_S938, Centre de Recherche Saint-Antoine, Institute of Cardiometabolism and Nutrition, Paris, France anne-claire.guenantin@inserm.fr nolwenn.briand@inserm.fr.
Emilie CapelSorbonne Universités, Université Pierre et Marie Curie, INSERM UMR_S938, Centre de Recherche Saint-Antoine, Institute of Cardiometabolism and Nutrition, Paris, France.
Florent DumontInstitut Cochin, Université Paris Descartes, INSERM U1016, Paris, France.
Romain MorichonSorbonne Universités, Université Pierre et Marie Curie, INSERM UMR_S938, Centre de Recherche Saint-Antoine, Institute of Cardiometabolism and Nutrition, Paris, France.
Claire ProvostPlateforme LIMP, UMS28 Phénotypage du petit animal, Université Pierre et Marie Curie, Paris, France.
Francesca StillitanoCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Dorota JeziorowskaSorbonne Universités, Université Pierre et Marie Curie, UMR_S1166, Institute of Cardiometabolism and Nutrition, France.
Jean-Pierre SiffroiSorbonne Universités, Université Pierre et Marie Curie, Assistance Publique-Hôspitaux de Paris, Service de Génétique et d'Embryologie Médicales, Hôpital Trousseau, Paris, France.
Roger J HajjarCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Bruno FèveSorbonne Universités, Université Pierre et Marie Curie, INSERM UMR_S938, Centre de Recherche Saint-Antoine, Institute of Cardiometabolism and Nutrition, Paris, France.
Jean-Sébastien HulotCardiovascular Research Center, Icahn School of Medicine at Mount Sinai, New York, NY.
Philippe CollasDepartment of Molecular Medicine, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Oslo, Norway.
Jacqueline CapeauSorbonne Universités, Université Pierre et Marie Curie, INSERM UMR_S938, Centre de Recherche Saint-Antoine, Institute of Cardiometabolism and Nutrition, Paris, France.
Corinne VigourouxSorbonne Universités, Université Pierre et Marie Curie, INSERM UMR_S938, Centre de Recherche Saint-Antoine, Institute of Cardiometabolism and Nutrition, Paris, France.ORCID 0000-0002-8181-4721
Inserm · FRSorbonne Université · FRIcahn School of Medicine at Mount Sinai · USOslo University Hospital · NO

Funding

TRIP: Targeted Gene Therapy for the Treatment of Heart FailureP50HL112324 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ASCHEIM, DEBORAH DAVIS, HAJJAR, ROGER J. · 2012 to 2014
$6.4M
SUMO1 and SERCA2a FunctionR01HL117505 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI WEBER, THOMAS · 2013 to 2020
$3.4M
Targeting Abnormal Calcium Cycling Using Novel Gene Therapy VectorsR01HL119046 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI AKAR, FADI GABRIEL, HAJJAR, ROGER J. · 2014 to 2017
$2.9M
NHLBI NIH HHS HHSN268201000045CNHLBI NIH HHS P50 HL112324NHLBI NIH HHS R01 HL117505NHLBI NIH HHS R01 HL119046
6 · The paper itself

Abstract

Activation of thermogenic beige adipocytes has recently emerged as a promising therapeutic target in obesity and diabetes. Relevant human models for beige adipocyte differentiation are essential to implement such therapeutic strategies. We report a straightforward and efficient protocol to generate functional human beige adipocytes from human induced pluripotent stem cells (hiPSCs). Without overexpression of exogenous adipogenic genes, our method recapitulates an adipogenic developmental pathway through successive mesodermal and adipogenic progenitor stages. hiPSC-derived adipocytes are insulin sensitive and display beige-specific markers and functional properties, including upregulation of thermogenic genes, increased mitochondrial content, and increased oxygen consumption upon activation with cAMP analogs. Engraftment of hiPSC-derived adipocytes in mice produces well-organized and vascularized adipose tissue, capable of β-adrenergic-responsive glucose uptake. Our model of human beige adipocyte development provides a new and scalable tool for disease modeling and therapeutic screening.

Indexed as

Insulin ResistanceObesityAdipocytes, BeigeAdipogenesisAdipose TissueAdrenergic beta-AgonistsAnimalsCell TransplantationCellular Reprogramming TechniquesFluorodeoxyglucose F18Gene Expression ProfilingGlucoseHumansInduced Pluripotent Stem CellsIsoproterenolMiceAdrenergic beta-AgonistsFluorodeoxyglucose F18GlucoseIsoproterenolRadiopharmaceuticalsRNA, Messenger

Identifiers

PMID28270520
PMCPMC5440013
OpenAlexW2593931721

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.