Evidence map›Paper›PMID 30265241›Full record

ArticleeLife2018

Identification of functionally distinct fibro-inflammatory and adipogenic stromal subpopulations in visceral adipose tissue of adult mice.

Chelsea Hepler, Bo Shan, Qianbin Zhang, Gervaise H Henry, Mengle Shao, Lavanya Vishvanath, Alexandra L Ghaben, Angela B Mobley, Douglas Strand, Gary C Hon and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 233 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
233citing papers in PubMed, 2 pooled it
17.3field-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

233 citing papers in PubMed, 2 syntheses or guidelines pooled it, 338 citations in OpenAlex.

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173 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

11 authors at 1 institution in 1 country.

Chelsea Hepler *Touchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0001-9938-382X
Bo ShanTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, United States.
Qianbin ZhangTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, United States.
Gervaise H HenryDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0001-7772-9578
Mengle ShaoTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0002-5488-9904
Lavanya VishvanathTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, United States.
Alexandra L GhabenTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0001-7377-7820
Angela B MobleyDepartment of Immunology, University of Texas Southwestern Medical Center, Dallas, United States.
Douglas StrandDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0002-0746-927X
Gary C HonCecil H. and Ida Green Center for Reproductive Biology Sciences, Division of Basic Reproductive Biology Research, Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, United States.
Rana K GuptaTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0002-9001-4531
The University of Texas Southwestern Medical Center · US

Funding

DIVISION OF CELL &MOLECULAR BIOLOGY TRAINING PROGRAMT32GM008203 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 1987 to 2018
$7.0M
Establishment and Maintenance of Healthy Adipose Tissue in ObesityR01DK104789 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GUPTA, RANA K · 2015 to 2024
$3.9M
Combinatorial Biology of Gene Regulation for Cellular EngineeringDP2GM128203 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI HON, GARY CHUNG · 2017 to 2021
$2.9M
Mechanisms of Fatty Acid Metabolism in Prostate Differentiation and DiseaseK01DK098277 · NIDDK · VANDERBILT UNIVERSITY · PI STRAND, DOUGLAS WILLIAM · 2013 to 2017
$640k
Interplay Between Stem Cells and Inflammation in Benign Prostatic HyperplasiaR03DK110497 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI STRAND, DOUGLAS WILLIAM · 2016 to 2017
$162k
Mural Cell Zfp423 in Control of Adipose Remodeling in ObesityF31DK113696 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI HEPLER, CHELSEA · 2017 to 2018
$51k
American Heart Association 16POST26420136Cancer Prevention and Research Institute of Texas RR140023NIDDK NIH HHS F31 DK113696NIDDK NIH HHS K01 DK098277NIDDK NIH HHS R01 DK104789NIDDK NIH HHS R03 DK110497NIGMS NIH HHS DP2 GM128203NIGMS NIH HHS DP2GM128203NIGMS NIH HHS T32 GM008203NIH HHS DK098277NIH HHS DK104789NIH HHS DK110497NIH HHS F31DK113696Welch Foundation I-1926-20170325
6 · The paper itself

Abstract

White adipose tissue (WAT) remodeling is dictated by coordinated interactions between adipocytes and resident stromal-vascular cells; however, the functional heterogeneity of adipose stromal cells has remained unresolved. We combined single-cell RNA-sequencing and FACS to identify and isolate functionally distinct subpopulations of PDGFRβ+ stromal cells within visceral WAT of adult mice. LY6C- CD9- PDGFRβ+ cells represent highly adipogenic visceral adipocyte precursor cells ('APCs'), whereas LY6C+ PDGFRβ+ cells represent fibro-inflammatory progenitors ('FIPs'). FIPs lack adipogenic capacity, display pro-fibrogenic/pro-inflammatory phenotypes, and can exert an anti-adipogenic effect on APCs. The pro-inflammatory phenotype of PDGFRβ+ cells is regulated, at least in part, by NR4A nuclear receptors. These data highlight the functional heterogeneity of visceral WAT perivascular cells, and provide insight into potential cell-cell interactions impacting adipogenesis and inflammation. These improved strategies to isolate FIPs and APCs from visceral WAT will facilitate the study of physiological WAT remodeling and mechanisms leading to metabolic dysfunction. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed.

Indexed as

AdipogenesisAdipocytesAdipose Tissue, WhiteAgingAnimalsAntigens, LyCell DifferentiationCell SeparationDiet, High-FatFemaleFibrosisGene Expression ProfilingGreen Fluorescent ProteinsInflammationIntra-Abdominal FatMaleAntigens, LyGreen Fluorescent ProteinsLy-6C antigen, mouseReceptor, Platelet-Derived Growth Factor betaTetraspanin 29adipogenesisadipose tissuefibrosishuman biologyinflammationmedicinemousemural cellsobesity

Identifiers

PMID30265241
PMCPMC6167054
OpenAlexW2893679529

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.