Evidence map›Paper›PMID 31420514›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Diverse repertoire of human adipocyte subtypes develops from transcriptionally distinct mesenchymal progenitor cells.

So Yun Min, Anand Desai, Zinger Yang, Agastya Sharma, Tiffany DeSouza, Ryan M J Genga, Alper Kucukural, Lawrence M Lifshitz, Søren Nielsen, Camilla Scheele and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed, 2 pooled it
12.7field-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

86 citing papers in PubMed, 2 syntheses or guidelines pooled it, 149 citations in OpenAlex.

  1. Pooled it
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  7. Advances in Adipose Tissue Biology.Endocrine reviews · 2026
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26 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

13 authors at 2 institutions in 2 countries.

So Yun MinProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655.ORCID 0000-0002-7949-1396
Anand DesaiProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655.
Zinger YangProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655.
Agastya SharmaProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655.
Tiffany DeSouzaProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655.
Ryan M J GengaProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655.
Alper KucukuralProgram in Bioinformatics, University of Massachusetts Medical School, Worcester, MA 01655.
Lawrence M LifshitzProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655.
Søren NielsenCentre of Inflammation and Metabolism, Rigshospitalet, University of Copenhagen, 1165 Copenhagen Denmark.
Camilla ScheeleCentre of Inflammation and Metabolism, Rigshospitalet, University of Copenhagen, 1165 Copenhagen Denmark.ORCID 0000-0002-6055-9709
René MaehrProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655.
Manuel GarberProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655.
Silvia CorveraProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01655; Silvia.Corvera@umassmed.edu.ORCID 0000-0002-0009-4129
University of Massachusetts Chan Medical School · USUniversity of Copenhagen · DK

Funding

University of Massachusetts Center for Clinical and Translational ScienceUL1TR000161 · NCATS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LUZURIAGA, KATHERINE F · 2012 to 2015
$11.0M
Adipose Tissue Angiogenesis and Metabolic DiseaseR01DK089101 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CORVERA, SILVIA · 2011 to 2024
$5.7M
Mechanisms of human adipose tissue development and impact of diabetesR01DK123028 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Silvia Corvera · 2019 to 2026
$3.6M
NCATS NIH HHS UL1 TR000161NIDDK NIH HHS R01 DK089101NIDDK NIH HHS R01 DK123028
6 · The paper itself

Abstract

Single-cell sequencing technologies have revealed an unexpectedly broad repertoire of cells required to mediate complex functions in multicellular organisms. Despite the multiple roles of adipose tissue in maintaining systemic metabolic homeostasis, adipocytes are thought to be largely homogenous with only 2 major subtypes recognized in humans so far. Here we report the existence and characteristics of 4 distinct human adipocyte subtypes, and of their respective mesenchymal progenitors. The phenotypes of these distinct adipocyte subtypes are differentially associated with key adipose tissue functions, including thermogenesis, lipid storage, and adipokine secretion. The transcriptomic signature of "brite/beige" thermogenic adipocytes reveals mechanisms for iron accumulation and protection from oxidative stress, necessary for mitochondrial biogenesis and respiration upon activation. Importantly, this signature is enriched in human supraclavicular adipose tissue, confirming that these cells comprise thermogenic depots in vivo, and explain previous findings of a rate-limiting role of iron in adipose tissue browning. The mesenchymal progenitors that give rise to beige/brite adipocytes express a unique set of cytokines and transcriptional regulators involved in immune cell modulation of adipose tissue browning. Unexpectedly, we also find adipocyte subtypes specialized for high-level expression of the adipokines adiponectin or leptin, associated with distinct transcription factors previously implicated in adipocyte differentiation. The finding of a broad adipocyte repertoire derived from a distinct set of mesenchymal progenitors, and of the transcriptional regulators that can control their development, provides a framework for understanding human adipose tissue function and role in metabolic disease.

Indexed as

ThermogenesisTranscriptomeAdipocytes, BeigeAdiponectinAdipose Tissue, BrownFemaleGene Expression ProfilingHumansLeptinMaleMesenchymal Stem CellsAdiponectinADIPOQ protein, humanLEP protein, humanLeptinadipocyte differentiationbrown adipocytehuman adipose tissuemesenchymal stem cellsprogenitor cells

Identifiers

PMID31420514
PMCPMC6731669
OpenAlexW2968499785

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.