Evidence map›Paper›PMID 33139957›Full record

ArticleNature metabolism2020

Perivascular mesenchymal cells control adipose-tissue macrophage accrual in obesity.

Bo Shan, Mengle Shao, Qianbin Zhang, Chelsea Hepler, Vivian A Paschoal, Spencer D Barnes, Lavanya Vishvanath, Yu A An, Lin Jia, Venkat S Malladi and 5 more

Open access · greenAbstract read
In one paragraph

Article in Nature metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

51 citing papers in PubMed, 84 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 1 country.

Bo Shan *Touchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-1675-5809
Mengle Shao *Touchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-5488-9904
Qianbin ZhangTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Chelsea HeplerTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0001-9938-382X
Vivian A PaschoalTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Spencer D BarnesLyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Lavanya VishvanathTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Yu A AnTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-9678-3382
Lin JiaCenter for Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, USA.
Venkat S MalladiLyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-0144-0564
Douglas W StrandDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-0746-927X
Olga T GuptaTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Joel K ElmquistCenter for Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, USA.
Dayoung OhTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-0687-6479
Rana K GuptaTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA. Rana.Gupta@UTSouthwestern.edu.ORCID http://orcid.org/0000-0002-9001-4531
The University of Texas Southwestern Medical Center · USSouthwestern Medical Center · US

Funding

Novel Mechanisms Regulating the Adipocyte-Brain-Hepatocyte AxisP01DK088761 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI HORTON, JAY D. · 2010 to 2019
$17.4M
Generation of Novel Genetic Tools to Study Cellular Heterogeneity in Adipose TissuesRC2DK118620 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GUPTA, RANA K, SCHERER, PHILIPP E · 2019 to 2023
$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
Feed-forward regulation between GPR120 and PPAR gamma - Revision - 1R01DK108773 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI OH, DAYOUNG · 2017 to 2021
$2.2M
Notch-mediated 5ARI resistance in human BPHR01DK115477 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI STRAND, DOUGLAS WILLIAM · 2018 to 2022
$1.9M
Multifaceted Roles for Pdgfrb+ Perivascular Cells in White Adipose Tissue RemodelingR01DK119163 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GUPTA, RANA K · 2019 to 2022
$1.8M
Role of Hepatocyte TLR4 in Alcohol-induced Steatohepatitis and Insulin ResistanceK01AA024809 · NIAAA · UT SOUTHWESTERN MEDICAL CENTER · PI JIA, LIN · 2017 to 2020
$598k
Peritoneal mesothelial cells: Role in obesity and metabolic dysfunctionR03DK101865 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GUPTA, OLGA THERESA · 2015 to 2017
$572k
Multifaceted Roles for Pdgfrb+ Perivascular Cells in White Adipose Tissue RemodelingR56DK119163 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GUPTA, RANA K · 2018 to 2018
$405k
Mural Cell Zfp423 in Control of Adipose Remodeling in ObesityF31DK113696 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI HEPLER, CHELSEA · 2017 to 2018
$51k
NIAAA NIH HHS K01 AA024809NIDDK NIH HHS F31 DK113696NIDDK NIH HHS P01 DK088761NIDDK NIH HHS R01 DK104789NIDDK NIH HHS R01 DK108773NIDDK NIH HHS R01 DK115477NIDDK NIH HHS R01 DK119163NIDDK NIH HHS R03 DK101865NIDDK NIH HHS R56 DK119163NIDDK NIH HHS RC2 DK118620
6 · The paper itself

Abstract

Chronic low-grade white adipose tissue (WAT) inflammation is a hallmark of metabolic syndrome in obesity. Here, we demonstrate that a subpopulation of mouse WAT perivascular (PDGFRβ

Indexed as

Mesenchymal Stem CellsAdipose Tissue, WhiteAnimalsDiet, High-FatDNA-Binding ProteinsHypoglycemic AgentsInsulinMacrophagesMiceMice, Inbred C57BLObesityReceptor, Platelet-Derived Growth Factor betaSignal TransductionToll-Like Receptor 4Transcription Factor RelATranscription FactorsDNA-Binding ProteinsEbfaz protein, mouseHypoglycemic AgentsInsulinReceptor, Platelet-Derived Growth Factor betaTlr4 protein, mouseToll-Like Receptor 4Transcription Factor RelATranscription Factors

Identifiers

PMID33139957
PMCPMC7669663
OpenAlexW3096518442

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.