Evidence map›Paper›PMID 27408774›Full record

ArticleMolecular metabolism2016

Lipodystrophy and severe metabolic dysfunction in mice with adipose tissue-specific insulin receptor ablation.

Guifen Qiang, Hyerim Whang Kong, Shanshan Xu, Hoai An Pham, Sebastian D Parlee, Aaron A Burr, Victoria Gil, Jingbo Pang, Amy Hughes, Xuejiang Gu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Review
  3. Obesity, diabetes and risk of bone fragility: How BMAT behavior is affected by metabolic disturbances and its influence on bone health.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. The benefits of adipocyte metabolism in bone health and regeneration.Frontiers in cell and developmental biology · 2023
    Review
  9. Article
  10. Adipocyte GNature communications · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Anti-Lipolysis Induced by Insulin in Diverse Pathophysiologic Conditions of Adipose Tissue.Diabetes, metabolic syndrome and obesity : targets and therapy · 2020
    Review
  17. Insulin Signaling in Bone Marrow Adipocytes.Current osteoporosis reports · 2019
    Review
  18. Article
  19. Article
  20. Article
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 2 institutions in 1 country.

Guifen QiangDepartment of Physiology & Biophysics, University of Illinois at Chicago, Chicago, IL, USA.
Hyerim Whang KongDepartment of Physiology & Biophysics, University of Illinois at Chicago, Chicago, IL, USA.
Shanshan XuDepartment of Physiology & Biophysics, University of Illinois at Chicago, Chicago, IL, USA.
Hoai An PhamDepartment of Molecular & Integrative Physiology, University of Michigan, Ann Arbor, MI, USA.
Sebastian D ParleeDepartment of Molecular & Integrative Physiology, University of Michigan, Ann Arbor, MI, USA.
Aaron A BurrDepartment of Molecular & Integrative Physiology, University of Michigan, Ann Arbor, MI, USA.
Victoria GilDepartment of Physiology & Biophysics, University of Illinois at Chicago, Chicago, IL, USA.
Jingbo PangDepartment of Kinesiology and Nutrition, University of Illinois at Chicago, Chicago, IL, USA.
Amy HughesDepartment of Physiology & Biophysics, University of Illinois at Chicago, Chicago, IL, USA.
Xuejiang GuDepartment of Physiology & Biophysics, University of Illinois at Chicago, Chicago, IL, USA.
Giamila FantuzziDepartment of Kinesiology and Nutrition, University of Illinois at Chicago, Chicago, IL, USA.
Ormond A MacDougaldDepartment of Molecular & Integrative Physiology, University of Michigan, Ann Arbor, MI, USA.
Chong Wee LiewDepartment of Physiology & Biophysics, University of Illinois at Chicago, Chicago, IL, USA. Electronic address: cwliew@uic.edu.
University of Illinois Chicago · USUniversity of Michigan–Ann Arbor · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Interdisciplinary Study of Marrow Adiposity, Mineral Metabolism & Energy BalanceR24DK092759 · NIDDK · MAINEHEALTH · PI HOROWITZ, MARK C, MACDOUGALD, ORMOND A · 2011 to 2019
$13.0M
TRAINING PROGRAM IN ORGANOGENESIST32HD007505 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PASCA DI MAGLIANO, MARINA, SPENCE, JASON · 1997 to 2021
$6.9M
Roles for Wnt Signaling in Adipose TissueR01DK062876 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MACDOUGALD, ORMOND A · 2003 to 2018
$5.1M
Role of Sweet Taste Receptors in Adipocyte Differentiation and MetabolismR01DK095705 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MACDOUGALD, ORMOND A · 2012 to 2015
$1.3M
Role of the transcriptional coregulator, TRIP Br2, in adipocyte metabolismR00DK090210 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LIEW, CHONG WEE · 2012 to 2014
$724k
Roles for Wnt signaling in adipose tissueR56DK062876 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MACDOUGALD, ORMOND A · 2008 to 2008
$225k
NICHD NIH HHS T32 HD007505NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R00 DK090210NIDDK NIH HHS R01 DK062876NIDDK NIH HHS R01 DK095705NIDDK NIH HHS R24 DK092759NIDDK NIH HHS R56 DK062876
6 · The paper itself

Abstract

objectiveInsulin signaling plays pivotal roles in the development and metabolism of many tissues and cell types. A previous study demonstrated that ablation of insulin receptor (IR) with aP2-Cre markedly reduced adipose tissues mass and protected mice from obesity. However, multiple studies have demonstrated widespread non-adipocyte recombination of floxed alleles in aP2-Cre mice. These findings underscore the need to re-evaluate the role of IR in adipocyte and systemic metabolism with a more adipose tissue-specific Cre mouse line.

methodsWe generated and phenotyped a new adipose tissue-specific IR mouse model using the adipose tissue-specific Adipoq-Cre line.

resultsHere we show that the Adipoq-Cre-mediated IR KO in mice leads to lipodystrophy and metabolic dysfunction, which is in stark contrast to the previous study. In contrast to white adipocytes, absence of insulin signaling does not affect development of marrow and brown adipocytes, but instead is required for lipid accumulation particularly for the marrow adipocytes. Lipodystrophic IR KO mice have profound insulin resistance, hyperglycemia, organomegaly, and impaired adipokine secretion.

conclusionsOur results demonstrate differential roles for insulin signaling for white, brown, and marrow adipocyte development and metabolic regulation.

Indexed as

Brown adipose tissueInsulin signalingLipodystrophyMarrow adipose tissueWhite adipose tissue

Identifiers

PMID27408774
PMCPMC4921803
OpenAlexW2351429842

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.