Evidence map›Paper›PMID 25594176›Full record

ArticleCell2015

Leptin and insulin act on POMC neurons to promote the browning of white fat.

Garron T Dodd, Stephanie Decherf, Kim Loh, Stephanie E Simonds, Florian Wiede, Eglantine Balland, Troy L Merry, Heike Münzberg, Zhong-Yin Zhang, Barbara B Kahn and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 227 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
227citing papers in PubMed, 1 pooled it
27.3field-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

227 citing papers in PubMed, 1 synthesis or guideline pooled it, 380 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Advances in research on thermogenic substances.Journal of physiological anthropology · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Central leptin pathways in metabolic homeostasis.Clinical science (London, England : 1979) · 2025
    Review
  16. Review
  17. The potential role of hypothalamic POMCExperimental & molecular medicine · 2025
    Article
  18. Article
  19. Article
  20. Review

167 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

15 authors at 6 institutions in 3 countries.

Garron T DoddDepartment of Biochemistry and Molecular Biology, Monash University, Victoria 3800, Australia.
Stephanie DecherfDepartment of Biochemistry and Molecular Biology, Monash University, Victoria 3800, Australia.
Kim LohDepartment of Biochemistry and Molecular Biology, Monash University, Victoria 3800, Australia.
Stephanie E SimondsDepartment of Physiology, Monash University, Victoria 3800, Australia.
Florian WiedeDepartment of Biochemistry and Molecular Biology, Monash University, Victoria 3800, Australia.
Eglantine BallandDepartment of Physiology, Monash University, Victoria 3800, Australia.
Troy L MerryDepartment of Biochemistry and Molecular Biology, Monash University, Victoria 3800, Australia.
Heike MünzbergPennington Biomedical Research Center, LSU Systems, Baton Rouge, LA 70808, USA.
Zhong-Yin ZhangDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Barbara B KahnDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02215, USA.
Benjamin G NeelCampbell Family Cancer Research Institute, Ontario Cancer Institute, Princess Margaret Hospital and Department of Medical Biophysics, University of Toronto, Toronto, ON M5G 2M9, Canada.
Kendra K BenceDepartment of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Zane B AndrewsDepartment of Physiology, Monash University, Victoria 3800, Australia.
Michael A CowleyDepartment of Physiology, Monash University, Victoria 3800, Australia.
Tony TiganisDepartment of Biochemistry and Molecular Biology, Monash University, Victoria 3800, Australia. Electronic address: tony.tiganis@monash.edu.
Monash University · AUBeth Israel Deaconess Medical Center · USIndiana University School of MedicinePennington Biomedical Research Center · USUniversity of Pennsylvania · USUniversity of Toronto · CA

Funding

The Arcuate Nucleus: A Genetic Assessment of FunctionP01DK056116 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KAHN, BARBARA B. · 1999 to 2010
$15.6M
Structure/Function of Protein Tyrosine PhosphatasesR01CA069202 · NCI · YESHIVA UNIVERSITY · PI Zhong-Yin Zhang · 1996 to 2026
$7.3M
Signal Transduction by Non-transmembrane PTPsR37CA049152 · NCI · UNIVERSITY HEALTH NETWORK · PI NEEL, BENJAMIN G. · 2004 to 2013
$4.0M
Neuronal Protein Tyrosine Phosphatases in MetabolismR01DK082417 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI BENCE, KENDRA · 2009 to 2015
$2.6M
Metabolic effects of adipose lipogenesisR01DK098002 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KAHN, BARBARA B., MCGRAW, TIMOTHY E · 2013 to 2016
$2.4M
Targeting PRL Phosphatases for Cancer TherapyR01CA126937 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI ZHANG, ZHONG-YIN · 2008 to 2012
$1.5M
NCI NIH HHS R01 CA069202NCI NIH HHS R01 CA126937NCI NIH HHS R01-CA69202NCI NIH HHS R37 CA049152NCI NIH HHS R37-CA49152NIDDK NIH HHS P01 DK056116NIDDK NIH HHS R01 DK082417NIDDK NIH HHS R01-DK082417NIDDK NIH HHS R01 DK098002NIDDK NIH HHS R01-DK98002
6 · The paper itself

Abstract

The primary task of white adipose tissue (WAT) is the storage of lipids. However, "beige" adipocytes also exist in WAT. Beige adipocytes burn fat and dissipate the energy as heat, but their abundance is diminished in obesity. Stimulating beige adipocyte development, or WAT browning, increases energy expenditure and holds potential for combating metabolic disease and obesity. Here, we report that insulin and leptin act together on hypothalamic neurons to promote WAT browning and weight loss. Deletion of the phosphatases PTP1B and TCPTP enhanced insulin and leptin signaling in proopiomelanocortin neurons and prevented diet-induced obesity by increasing WAT browning and energy expenditure. The coinfusion of insulin plus leptin into the CNS or the activation of proopiomelanocortin neurons also increased WAT browning and decreased adiposity. Our findings identify a homeostatic mechanism for coordinating the status of energy stores, as relayed by insulin and leptin, with the central control of WAT browning.

Indexed as

Adipose Tissue, BrownAdipose Tissue, WhiteAdiposityAnimalsBody Temperature RegulationInsulinLeptinMice, Inbred C57BLMice, KnockoutNeuronsObesityPro-OpiomelanocortinProtein Tyrosine Phosphatase, Non-Receptor Type 1Protein Tyrosine Phosphatase, Non-Receptor Type 2InsulinLeptinPro-OpiomelanocortinProtein Tyrosine Phosphatase, Non-Receptor Type 1Protein Tyrosine Phosphatase, Non-Receptor Type 2Ptpn1 protein, mouse

Identifiers

PMID25594176
PMCPMC4453004
OpenAlexW2078409165

What OpenQuestion holds

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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.