Evidence map›Paper›PMID 28414329›Full record

ArticleNature medicine2017

Alternatively activated macrophages do not synthesize catecholamines or contribute to adipose tissue adaptive thermogenesis.

Katrin Fischer, Henry H Ruiz, Kevin Jhun, Brian Finan, Douglas J Oberlin, Verena van der Heide, Anastasia V Kalinovich, Natasa Petrovic, Yochai Wolf, Christoffer Clemmensen and 19 more

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 209 papers.

0numbers the graph read from it
0cells of the map it votes in
209citing papers in PubMed
29.1field-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

209 citing papers in PubMed, 323 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Adipose-Tissue Macrophage Diversity and Functions.International journal of molecular sciences · 2026
    Review
  8. Article
  9. Weight Loss-Associated Remodeling of Adipose Tissue Immunometabolism.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Thermogenic Adipocytes Promote M2 Macrophage Polarization through CNNM4-Mediated Mg Secretion.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  18. Review
  19. Review
  20. Review

149 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

29 authors at 10 institutions in 5 countries.

Katrin FischerInstitute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC) at Helmholtz Zentrum München and German Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany.
Henry H RuizDiabetes, Metabolism and Obesity Institute, Icahn School of Medicine at Mount Sinai, NY 10029, USA.
Kevin JhunDiabetes, Metabolism and Obesity Institute, Icahn School of Medicine at Mount Sinai, NY 10029, USA.
Brian FinanInstitute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC) at Helmholtz Zentrum München and German Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany.
Douglas J OberlinDiabetes, Metabolism and Obesity Institute, Icahn School of Medicine at Mount Sinai, NY 10029, USA.
Verena van der HeideDiabetes, Metabolism and Obesity Institute, Icahn School of Medicine at Mount Sinai, NY 10029, USA.
Anastasia V KalinovichDepartment of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, 10691 Stockholm, Sweden.
Natasa PetrovicDepartment of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, 10691 Stockholm, Sweden.
Yochai WolfWeizmann Institute of Science Department of Immunology, 76100 Rehovot, Israel.
Christoffer ClemmensenInstitute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC) at Helmholtz Zentrum München and German Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany.
Andrew C ShinDiabetes, Metabolism and Obesity Institute, Icahn School of Medicine at Mount Sinai, NY 10029, USA.
Senad DivanovicDepartment of Pediatrics, Division of Immunobiology, Cincinnati Children's Hospital Medical Center, OH 45229 Cincinnati, USA.
Frank BrombacherInternational Center for Genetic Engineering and Biotechnology, Cape Town component & University of Cape Town, IDM, Division Immunology & SAMRC, South Africa.
Elke GlasmacherInstitute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC) at Helmholtz Zentrum München and German Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany.
Susanne KeipertInstitute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC) at Helmholtz Zentrum München and German Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany.
Martin JastrochInstitute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC) at Helmholtz Zentrum München and German Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany.
Joachim NaglerMolecular Exposomics, Helmholtz Zentrum München, German National Diabetes Center (DZD), 85764 Neuherberg, Germany.
Karl-Werner SchrammMolecular Exposomics, Helmholtz Zentrum München, German National Diabetes Center (DZD), 85764 Neuherberg, Germany.
Dasa MedrikovaInstitute for Diabetes and Cancer (IDC), Helmholtz Zentrum München, German National Diabetes Center (DZD), 85764 Neuherberg, Germany, and Joint IDC-Heidelberg Translational Diabetes Program, Inner Medicine I, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Gustav ColldenInstitute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC) at Helmholtz Zentrum München and German Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany.
Stephen C WoodsMetabolic Diseases Institute, Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati, OH 45237 Cincinnati, USA.
Stephan HerzigInstitute for Diabetes and Cancer (IDC), Helmholtz Zentrum München, German National Diabetes Center (DZD), 85764 Neuherberg, Germany, and Joint IDC-Heidelberg Translational Diabetes Program, Inner Medicine I, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Dirk HomannDiabetes, Metabolism and Obesity Institute, Icahn School of Medicine at Mount Sinai, NY 10029, USA.
Steffen JungWeizmann Institute of Science Department of Immunology, 76100 Rehovot, Israel.
Jan NedergaardDepartment of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, 10691 Stockholm, Sweden.
Barbara CannonDepartment of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, 10691 Stockholm, Sweden.
Matthias H TschöpInstitute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC) at Helmholtz Zentrum München and German Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany.
Timo D Müller *Institute for Diabetes and Obesity, Helmholtz Diabetes Center (HDC) at Helmholtz Zentrum München and German Center for Diabetes Research (DZD), 85764 München-Neuherberg, Germany.
Christoph Buettner *Diabetes, Metabolism and Obesity Institute, Icahn School of Medicine at Mount Sinai, NY 10029, USA.
Helmholtz Zentrum München · DEIcahn School of Medicine at Mount Sinai · USStockholm University · SEDeutsches Diabetes-Zentrum e.V. · DEHeidelberg University · DEWeizmann Institute of Science · ILCincinnati Children's Hospital Medical Center · USPhilipps University of Marburg · DESouth African Medical Research Council · ZAUniversity of Cincinnati · US

Funding

Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Kathryn Ann Wikenheiser-Brokamp · 2007 to 2026
$24.4M
Immunopathogenesis of Non-alcoholic Fatty Liver DiseaseR01DK099222 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Senad Divanovic · 2013 to 2026
$5.6M
INSULIN AND CNS CONTROL OF BODY WEIGHT AND FOOD INTAKER01DK017844 · NIDDK · UNIVERSITY OF WASHINGTON · PI WOODS, STEPHEN C · 1986 to 2013
$3.8M
A Role of Hypothalamic Dysfunction in Alcoholic Liver DiseaseR01AA023416 · NIAAA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BUETTNER, CHRISTOPH · 2014 to 2018
$2.2M
Regulation of Pathogen-specific T Cell Immunity by Adenosine GenerationR01AI093637 · NIAID · UNIVERSITY OF COLORADO DENVER · PI HOMANN, DIRK · 2012 to 2016
$2.0M
INSULIN AND CNS CONTROL OF BODY WEIGHT AND FOOD INTAKER37DK017844 · NIDDK · UNIVERSITY OF WASHINGTON · PI WOODS, STEPHEN C · 1993 to 2000
$382k
The role of the endocannabinoid system in regulating hepatic glucose fluxesR03DK082724 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BUETTNER, CHRISTOPH · 2009 to 2010
$169k
Regulation of Adipose Tissue Metabolism by Central Insulin and LeptinR56DK083658 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BUETTNER, CHRISTOPH · 2016 to 2016
$127k
European Research Council 340345NIAAA NIH HHS R01 AA023416NIAID NIH HHS R01 AI093637NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P30 DK078392NIDDK NIH HHS R01 DK017844NIDDK NIH HHS R01 DK099222NIDDK NIH HHS R03 DK082724NIDDK NIH HHS R37 DK017844NIDDK NIH HHS R56 DK083658
6 · The paper itself

Abstract

Adaptive thermogenesis is the process of heat generation in response to cold stimulation. It is under the control of the sympathetic nervous system, whose chief effector is the catecholamine norepinephrine (NE). NE enhances thermogenesis through β3-adrenergic receptors to activate brown adipose tissue and by 'browning' white adipose tissue. Recent studies have reported that alternative activation of macrophages in response to interleukin (IL)-4 stimulation induces the expression of tyrosine hydroxylase (TH), a key enzyme in the catecholamine synthesis pathway, and that this activation provides an alternative source of locally produced catecholamines during the thermogenic process. Here we report that the deletion of Th in hematopoietic cells of adult mice neither alters energy expenditure upon cold exposure nor reduces browning in inguinal adipose tissue. Bone marrow-derived macrophages did not release NE in response to stimulation with IL-4, and conditioned media from IL-4-stimulated macrophages failed to induce expression of thermogenic genes, such as uncoupling protein 1 (Ucp1), in adipocytes cultured with the conditioned media. Furthermore, chronic treatment with IL-4 failed to increase energy expenditure in wild-type, Ucp1

Indexed as

Adaptation, PhysiologicalAdipocytesAdipose TissueAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsBlotting, WesternBody CompositionCatecholaminesCell DifferentiationCulture Media, ConditionedEnergy MetabolismFlow CytometryFluorescent Antibody TechniqueGene Expression ProfilingInterleukin-4CatecholaminesCulture Media, ConditionedIl4ra protein, mouseInterleukin-4Interleukin-4 Receptor alpha SubunitNorepinephrineReceptors, Adrenergic, beta-3Receptors, Cell SurfaceTyrosine 3-MonooxygenaseUcp1 protein, mouseUncoupling Protein 1

Identifiers

PMID28414329
PMCPMC5420449
OpenAlexW2605827566

What OpenQuestion holds

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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.