Evidence map›Paper›PMID 24169547›Full record

ArticleEndocrinology2014

Bone marrow leptin signaling mediates obesity-associated adipose tissue inflammation in male mice.

Lea H Dib, M Teresa Ortega, Sherry D Fleming, Stephen K Chapes, Tonatiuh Melgarejo

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

42 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Review
  3. Special Issue "Hormone Signaling in Human Health and Diseases".International journal of molecular sciences · 2026
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
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  11. Role of adipose tissue macrophages in obesity-related disorders.The Journal of experimental medicine · 2022
    Article
  12. Review
  13. Review
  14. Review
  15. A Tale of Three Systems: Toward a Neuroimmunoendocrine Model of Obesity.Annual review of cell and developmental biology · 2021
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Lea H DibDepartment of Human Nutrition (L.H.D., T.M.) and Division of Biology (M.T.O., S.D.F., S.K.C.), Kansas State University, Manhattan, Kansas 66506.
M Teresa Ortega
Sherry D Fleming
Stephen K Chapes
Tonatiuh Melgarejo
Kansas State University · US

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SUSAN J. BROWN · 2012 to 2026
$63.0M
UNDERSTANDING THE ROLE OF SMALL RNAS IN ARABIDOPSIS POLLEN DEVELOPMENTP20RR016475 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ACKLEY, BRIAN DOUGLAS · 2001 to 2011
$38.1M
TRANSEPITHELIAL ION TRANSPORT &ITS REGULATIONP20RR017686 · NCRR · KANSAS STATE UNIVERSITY · PI MELGAREJO GARCIA, LUIS TONATIUH · 2002 to 2011
$21.8M
TRAFFICKING OF THE PLASMA MEMBRANE CA2+-ATPASE TO RAFTSP20RR017708 · NCRR · UNIVERSITY OF KANSAS LAWRENCE · PI FISCHER, CHRISTOPHER JAMES · 2002 to 2011
$20.1M
Natural Antibodies and Tissue InjuryR01AI061691 · NIAID · KANSAS STATE UNIVERSITY · PI FLEMING, SHERRY · 2007 to 2011
$1.7M
Definition of host genes required for intracellular pathogen growthR21AI088070 · NIAID · KANSAS STATE UNIVERSITY · PI CHAPES, STEPHEN KEITH, VON OHLEN, TONIA L · 2010 to 2011
$401k
NCRR NIH HHS P20 RR016475NCRR NIH HHS P20 RR017686NCRR NIH HHS P20 RR017708NCRR NIH HHS RR17708NIAID NIH HHS AI061691NIAID NIH HHS AI088070NIAID NIH HHS R01 AI061691NIAID NIH HHS R21 AI088070NIGMS NIH HHS P20 GM103418
6 · The paper itself

Abstract

Obesity is characterized by an increased recruitment of proinflammatory macrophages to the adipose tissue (AT), leading to systemic inflammation and metabolic disease. The pathogenesis of this AT inflammation, however, remains to be elucidated. The circulating adipokine leptin is increased in obesity and is involved in immune cell function and activation. In the present study, we investigated the role of leptin in the induction of obesity-associated inflammation. We generated radiation chimeric C57BL/6J mice reconstituted with either leptin receptor-deficient (db/db) or wild-type (WT) bone marrow and challenged them with a high-fat diet (HFD) for 16 weeks. Mice reconstituted with db/db bone marrow (WT/db), had significantly lower body weight and adiposity compared with mice with WT bone marrow (WT/WT). Gonadal AT in WT/db mice displayed a 2-fold lower expression of the inflammatory genes Tnfa, Il6, and Ccl2. In addition, gonadal fat of WT/db mice contained significantly fewer crown-like structures compared with WT/WT mice, and most of their AT macrophages expressed macrophage galactose-type C type lectin 1 (MGL1) and were C-C chemokine receptor type 2 (CCR2)-negative, indicative of an anti-inflammatory phenotype. Moreover, WT/db mice exhibited greater insulin sensitivity compared with WT/WT mice. These data show that disrupted leptin signaling in bone marrow-derived cells attenuates the proinflammatory conditions that mediate many of the metabolic complications that characterize obesity. Our findings establish a novel mechanism involved in the regulation of obesity-associated systemic inflammation and support the hypothesis that leptin is a proinflammatory cytokine.

Indexed as

Gene Expression RegulationAdipose TissueAnimal FeedAnimalsBody CompositionBone MarrowDiet, High-FatDisease Models, AnimalGene Expression ProfilingImmunohistochemistryInflammationLeptinMacrophagesMaleMiceMice, Inbred C57BLLeptinReceptors, Leptin

Identifiers

PMID24169547
PMCPMC3868799
OpenAlexW2063712929

What OpenQuestion holds

Textmetadata
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.