Evidence map›Paper›PMID 22044999›Full record

ArticleNature communications2011

Disrupted erythropoietin signalling promotes obesity and alters hypothalamus proopiomelanocortin production.

Ruifeng Teng, Oksana Gavrilova, Norio Suzuki, Tatyana Chanturiya, Daniel Schimel, Lynne Hugendubler, Selin Mammen, Dena R Yver, Samuel W Cushman, Elisabetta Mueller and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature communications, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

67 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
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  10. The Role of NADBiomedicines · 2023
    Review
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  12. Article
  13. Article
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  15. Article
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  18. Review
  19. Erythropoietin treatment and the risk of hip fractures in hemodialysis patients.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Article
  20. Article

7 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 6 institutions in 2 countries.

Ruifeng TengMolecular Cell Biology Branch, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892, USA.
Oksana Gavrilova
Norio Suzuki
Tatyana Chanturiya
Daniel Schimel
Lynne Hugendubler
Selin Mammen
Dena R Yver
Samuel W Cushman
Elisabetta Mueller
Masayuki Yamamoto
Lewis L Hsu
Constance Tom Noguchi
National Institutes of Health · USCore Laboratories (United States) · USTohoku University · JPCenter for Cancer and Blood Disorders · USNational Institute of Diabetes and Digestive and Kidney Diseases · USNational Institute of Neurological Disorders and Stroke · US

Funding

Metabolic Studies of Mouse Models of Obesity and DiabetesZICDK070002 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI GAVRILOVA, OKSANA · 2009 to 2025
$15.0M
Identification of novel transcriptional regulators of lipid metabolism.ZIADK056023 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI MUELLER, ELISABETTA · 2009 to 2016
$3.9M
Erythropoietin receptor and glucose metabolismZIADK025102 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI NOGUCHI, CONSTANCE · 2009 to 2015
$3.5M
Intramural NIH HHS ZIA DK025102
6 · The paper itself

Abstract

Although erythropoietin (Epo) is the cytokine known to regulate erythropoiesis, erythropoietin receptor (EpoR) expression and associated activity beyond haematopoietic tissue remain uncertain. Here we show that mice with EpoR expression restricted to haematopoietic tissues (Tg) develop obesity and insulin resistance. Tg-mice exhibit a decrease in energy expenditure and an increase in white fat mass and adipocyte number. Conversely, Epo treatment of wild-type (WT)-mice increases energy expenditure and reduces food intake and fat mass accumulation but shows no effect in body weight of Tg-mice. EpoR is expressed at a high level in white adipose tissue and in the proopiomelanocortin (POMC) neurons of the hypothalamus. Although Epo treatment in WT-mice induces the expression of the polypeptide hormone precursor, POMC, mice lacking EpoR show reduced levels of POMC in the hypothalamus. This study provides the first evidence that mice lacking EpoR in non-haematopoietic tissue become obese and insulin resistant with loss of Epo regulation of energy homeostasis.

Indexed as

AnimalsBlotting, WesternErythropoietinFemaleHypothalamusImmunohistochemistryMaleMiceMice, Inbred C57BLMice, TransgenicObesityPro-OpiomelanocortinReceptors, ErythropoietinReverse Transcriptase Polymerase Chain ReactionErythropoietinPro-OpiomelanocortinReceptors, Erythropoietin

Identifiers

PMID22044999
PMCPMC3542973
OpenAlexW1990521190

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.