Evidence map›Paper›PMID 35487210›Full record

ArticleStem cell reports2022

Prepubertal androgen signaling is required to establish male fat distribution.

Zachary L Sebo, Matthew S Rodeheffer

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Innervation of adipocytes is limited in mouse perivascular adipose tissue.American journal of physiology. Heart and circulatory physiology · 2024
    Article
  5. Article
  6. 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

2 authors at 2 institutions in 1 country.

Zachary L SeboDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA; Department of Comparative Medicine, Yale University School of Medicine, 375 Congress Ave, New Haven, CT 06520, USA; Yale Program in Integrative Cell Signaling and Neurobiology of Metabolism, Yale University, New Haven, CT, USA.
Matthew S RodehefferDepartment of Comparative Medicine, Yale University School of Medicine, 375 Congress Ave, New Haven, CT 06520, USA; Department of Cellular and Molecular Physiology, Yale University, New Haven, CT, USA; Yale Stem Cell Center, Yale University, New Haven, CT, USA; Yale Program in Integrative Cell Signaling and Neurobiology of Metabolism, Yale University, New Haven, CT, USA. Electronic address: matthew.rodeheffer@yale.edu.
Yale Cancer Center · USYale University · US

Funding

Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI Richard A Flavell · 1993 to 2026
$44.0M
Cellular & molecular mechanisms of white adipose tissue mass regulationR01DK090489 · NIDDK · YALE UNIVERSITY · PI RODEHEFFER, MATTHEW S · 2011 to 2020
$3.8M
Dietary regulation of adipocyte hyperplasia in obesity: Impact on adipose mass and metabolic diseaseR01DK110147 · NIDDK · YALE UNIVERSITY · PI RODEHEFFER, MATTHEW S · 2016 to 2019
$1.9M
Cellular and molecular mechanisms of white adipose tissue regulation in development and diseaseR56DK090489 · NIDDK · YALE UNIVERSITY · PI RODEHEFFER, MATTHEW S · 2016 to 2016
$209k
NIDDK NIH HHS P30 DK045735NIDDK NIH HHS R01 DK090489NIDDK NIH HHS R01 DK110147NIDDK NIH HHS R56 DK090489
6 · The paper itself

Abstract

Fat distribution is sexually dimorphic and is associated with metabolic disease risk. It is unknown if prepubertal sex-hormone signaling influences adult fat distribution. Here, we show that karyotypically male androgen-insensitive mice exhibit pronounced subcutaneous adiposity compared with wild-type males and females. This subcutaneous adipose bias emerges prior to puberty and is not due to differences in adipocyte size or rates of adipogenesis between visceral and subcutaneous fat. Instead, we find that androgen-insensitive mice lack an adequate progenitor pool for normal visceral-fat expansion during development, thus increasing the subcutaneous-to-visceral-fat ratio. Obesogenic visceral-fat expansion is likewise inhibited in these mice, yet their metabolic health is similar to wild-type animals with comparable total fat mass. Taken together, these data show that adult fat distribution can be determined prior to the onset of puberty by the relative number of progenitors that seed nascent adipose depots.

Indexed as

Adipose TissueAndrogensAdipogenesisAdiposityAnimalsFemaleIntra-Abdominal FatMaleMiceAndrogensadipocyteadipocyte precursorsadiposeandrogenfat distributionobesityprogenitors

Identifiers

PMID35487210
PMCPMC9133643
OpenAlexW4224998955

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.