Evidence map›Paper›PMID 32755590›Full record

ArticleCell reports2020

Single-Cell RNA Profiling Reveals Adipocyte to Macrophage Signaling Sufficient to Enhance Thermogenesis.

Felipe Henriques, Alexander H Bedard, Adilson Guilherme, Mark Kelly, Jingyi Chi, Peng Zhang, Lawrence M Lifshitz, Karl Bellvé, Leslie A Rowland, Batuhan Yenilmez and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

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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 1 country.

Felipe HenriquesProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Alexander H BedardProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Adilson GuilhermeProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Mark KellyProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Jingyi ChiLaboratory of Molecular Metabolism, The Rockefeller University, New York, NY, USA.
Peng ZhangLife Sciences Institute, University of Michigan Medical Center, Ann Arbor, MI, USA; Department of Cell and Developmental Biology, University of Michigan Medical Center, Ann Arbor, MI, USA.
Lawrence M LifshitzProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Karl BellvéProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Leslie A RowlandProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Batuhan YenilmezProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Shreya KumarProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Yetao WangProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Jeremy LubanProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Lee S WeinsteinMetabolic Diseases Branch, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
Jiandie D LinLife Sciences Institute, University of Michigan Medical Center, Ann Arbor, MI, USA; Department of Cell and Developmental Biology, University of Michigan Medical Center, Ann Arbor, MI, USA.
Paul CohenLaboratory of Molecular Metabolism, The Rockefeller University, New York, NY, USA.
Michael P CzechProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA. Electronic address: michael.czech@umassmed.edu.
University of Massachusetts Chan Medical School · USAnn Arbor VA Medical Center · USRockefeller University · USNational Institutes of Health · US

Funding

Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Kanakadurga Singer · 2010 to 2026
$20.3M
Insulin Signaling and Metabolic Regulation in AdipocytesR37DK030898 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1996 to 2021
$7.2M
The HUSH complex in HIV-1 latencyR37AI147868 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI JEREMY LUBAN · 2019 to 2026
$6.4M
Paracrine Signaling by Kupffer Cells in Hepatic Insulin ResistanceR01DK103047 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 2015 to 2023
$5.0M
Role of the Gnas Gene in Metabolic RegulationZIADK043313 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI WEINSTEIN, LEE · 2009 to 2025
$4.9M
Metabolic crosstalk through brown fat-enriched secreted factorsR01DK102456 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jiandie D Lin · 2015 to 2026
$4.9M
The Origin, Dynamics, and Function of Postnatal Beige AdipocytesR01DK120649 · NIDDK · ROCKEFELLER UNIVERSITY · PI Paul Cohen · 2019 to 2026
$4.2M
Role of Gs-alpha in regulation of adipose tissue growth and functionZIADK043316 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI WEINSTEIN, LEE · 2009 to 2025
$3.4M
Adipocyte to neuron signaling in thermogenic programming of white adipose tissueR01DK116056 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 2019 to 2023
$2.9M
Insulin Signaling and Metabolic Regulation in AdipocytesR01DK030898 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1986 to 2011
$2.7M
NIAID NIH HHS R37 AI147868NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P30 DK089503NIDDK NIH HHS R01 DK030898NIDDK NIH HHS R01 DK102456NIDDK NIH HHS R01 DK103047NIDDK NIH HHS R01 DK116056NIDDK NIH HHS R01 DK120649NIDDK NIH HHS R37 DK030898
6 · The paper itself

Abstract

Adipocytes deficient in fatty acid synthase (iAdFASNKO) emit signals that mimic cold exposure to enhance the appearance of thermogenic beige adipocytes in mouse inguinal white adipose tissues (iWATs). Both cold exposure and iAdFASNKO upregulate the sympathetic nerve fiber (SNF) modulator Neuregulin 4 (Nrg4), activate SNFs, and require adipocyte cyclic AMP/protein kinase A (cAMP/PKA) signaling for beige adipocyte appearance, as it is blocked by adipocyte Gsα deficiency. Surprisingly, however, in contrast to cold-exposed mice, neither iWAT denervation nor Nrg4 loss attenuated adipocyte browning in iAdFASNKO mice. Single-cell transcriptomic analysis of iWAT stromal cells revealed increased macrophages displaying gene expression signatures of the alternately activated type in iAdFASNKO mice, and their depletion abrogated iWAT beiging. Altogether, these findings reveal that divergent cellular pathways are sufficient to cause adipocyte browning. Importantly, adipocyte signaling to enhance alternatively activated macrophages in iAdFASNKO mice is associated with enhanced adipose thermogenesis independent of the sympathetic neuron involvement this process requires in the cold.

Indexed as

Signal TransductionSingle-Cell AnalysisThermogenesisAdipocytes, BeigeAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsCell PolarityCold TemperatureCyclic AMPDenervationFatty Acid SynthasesMacrophage ActivationMacrophagesMaleMice, Inbred C57BLCyclic AMPFatty Acid Synthasesneuregulin-4NeuregulinsRNAUncoupling Protein 1beige adipocytesde novo lipogenesismacrophage polarizationstromal vascular fractionsympathetic nerve fibers

Identifiers

PMID32755590
PMCPMC7433376
OpenAlexW3047082745

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.