Evidence map›Paper›PMID 26808348›Full record

ArticleNature medicine2016

Human 'brite/beige' adipocytes develop from capillary networks, and their implantation improves metabolic homeostasis in mice.

So Yun Min, Jamie Kady, Minwoo Nam, Raziel Rojas-Rodriguez, Aaron Berkenwald, Jong Hun Kim, Hye-Lim Noh, Jason K Kim, Marcus P Cooper, Timothy Fitzgibbons and 2 more

Abstract read
In one paragraph

Article in Nature medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 171 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
171citing papers in PubMed, 2 pooled it
22.4field-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

171 citing papers in PubMed, 2 syntheses or guidelines pooled it, 306 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Commitment of adipose-resident c-kitNature communications · 2025
    Article
  18. Article
  19. Review
  20. Review

111 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

So Yun MinProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Jamie KadyProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Minwoo NamGraduate School of Biomedical Sciences, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Raziel Rojas-RodriguezProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Aaron BerkenwaldClinical Translational Research Pathway, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Jong Hun KimProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Hye-Lim NohProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Jason K KimProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Marcus P CooperCardiovascular Center of Excellence, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Timothy FitzgibbonsCardiovascular Center of Excellence, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Michael A BrehmProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Silvia CorveraProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.ORCID http://orcid.org/0000-0002-0009-4129
University of Massachusetts Chan Medical School · US

Funding

Systems Biology of Insulin ResistanceR24DK090963 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI DAVIS, ROGER J. · 2011 to 2014
$8.4M
Adipose Tissue Angiogenesis and Metabolic DiseaseR01DK089101 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CORVERA, SILVIA · 2011 to 2024
$5.7M
UMass Mouse Metabolic Phenotyping Center - Metabolism CoreU2CDK093000 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KIM, JASON K · 2016 to 2021
$4.6M
Development and Validation of Novel NSG Mouse Models for Human Stem Cell TherapyR24OD018259 · OD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, GREINER, DALE LESLIE · 2014 to 2017
$3.0M
UMass Mouse Metabolic Phenotyping CenterU24DK093000 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KIM, JASON K · 2011 to 2015
$2.1M
Mechanisms and metabolic implications of LRP130 in NAFLDR01DK089185 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI COOPER, MARCUS P · 2010 to 2014
$1.8M
Interleukin-10 and Regulation of Skeletal Muscle Insulin ActionR01DK080756 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KIM, JASON K · 2008 to 2012
$1.6M
Endoplasmic Reticulum Chaperone as a Regulator of Obesity and DiabetesR01DK079999 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LEE, AMY S · 2009 to 2010
$776k
NIDDK NIH HHS R01 DK079999NIDDK NIH HHS R01-DK079999NIDDK NIH HHS R01 DK080756NIDDK NIH HHS R01-DK080756NIDDK NIH HHS R01 DK089101NIDDK NIH HHS R01DK089101NIDDK NIH HHS R01 DK089185NIDDK NIH HHS R01DK089185NIDDK NIH HHS R24 DK090963NIDDK NIH HHS R24-DK090963NIDDK NIH HHS U24 DK093000NIDDK NIH HHS U24-DK093000NIDDK NIH HHS U2C DK093000NIH HHS R24 OD018259NIH HHS R24OD018259
6 · The paper itself

Abstract

Uncoupling protein 1 (UCP1) is highly expressed in brown adipose tissue, where it generates heat by uncoupling electron transport from ATP production. UCP1 is also found outside classical brown adipose tissue depots, in adipocytes that are termed 'brite' (brown-in-white) or 'beige'. In humans, the presence of brite or beige (brite/beige) adipocytes is correlated with a lean, metabolically healthy phenotype, but whether a causal relationship exists is not clear. Here we report that human brite/beige adipocyte progenitors proliferate in response to pro-angiogenic factors, in association with expanding capillary networks. Adipocytes formed from these progenitors transform in response to adenylate cyclase activation from being UCP1 negative to being UCP1 positive, which is a defining feature of the beige/brite phenotype, while displaying uncoupled respiration. When implanted into normal chow-fed, or into high-fat diet (HFD)-fed, glucose-intolerant NOD-scid IL2rg(null) (NSG) mice, brite/beige adipocytes activated in vitro enhance systemic glucose tolerance. These adipocytes express neuroendocrine and secreted factors, including the pro-protein convertase PCSK1, which is strongly associated with human obesity. Pro-angiogenic conditions therefore drive the proliferation of human beige/brite adipocyte progenitors, and activated beige/brite adipocytes can affect systemic glucose homeostasis, potentially through a neuroendocrine mechanism.

Indexed as

Neovascularization, PhysiologicOxygen ConsumptionAdipocytesAdipocytes, BrownAdipocytes, WhiteAdultAgedAnimalsApoptosis Regulatory ProteinsBlood GlucoseCapillariesCell TransplantationDiet, High-FatDNA-Binding ProteinsEnkephalinsFemaleApoptosis Regulatory ProteinsBlood GlucoseCIDEA protein, humanDNA-Binding ProteinsEnkephalinsIL33 protein, humanIntegrin beta1Interleukin-33Iodide PeroxidaseIodothyronine Deiodinase Type IIIon ChannelsMitochondrial Proteinsornithine decarboxylase antizymePCSK1 protein, humanproenkephalinProprotein Convertase 1Protein PrecursorsProteinsReceptor, Platelet-Derived Growth Factor alphaRNA, MessengerUCP1 protein, humanUcp1 protein, mouseUncoupling Protein 1

Identifiers

PMID26808348
PMCPMC4777633
OpenAlexW2252280064

What OpenQuestion holds

Textmetadata
LicenceTDM
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.