Evidence map›Paper›PMID 28649987›Full record

ArticleNature communications2017

A PPARγ transcriptional cascade directs adipose progenitor cell-niche interaction and niche expansion.

Yuwei Jiang, Daniel C Berry, Ayoung Jo, Wei Tang, Robert W Arpke, Michael Kyba, Jonathan M Graff

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

41 citing papers in PubMed, 53 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Yuwei JiangDivision of Endocrinology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Daniel C BerryDivision of Endocrinology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Ayoung JoDepartment of Developmental Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Wei TangDepartment of Developmental Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Robert W ArpkeLillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Michael KybaLillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota 55455, USA.ORCID 0000-0002-5579-7534
Jonathan M GraffDivision of Endocrinology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
The University of Texas Southwestern Medical Center · USUniversity of Minnesota · US

Funding

Biomarkers, Lineage Analysis--metabolic disease statesR01DK066556 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GRAFF, JONATHAN M · 2003 to 2017
$5.3M
Invertebrate Models of Fat StorageR01DK064261 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GRAFF, JONATHAN M · 2003 to 2014
$3.3M
Hormonal Regulation of Fat DepositionR01DK088220 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GRAFF, JONATHAN M · 2010 to 2014
$2.6M
Molecular regulation of adipose tissue development, homeostasis and expansionK01DK111771 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI JIANG, YUWEI · 2016 to 2021
$705k
Regulators of the adipose tissue niche control adiposity and metabolismK01DK109027 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI BERRY, DANIEL CARL · 2016 to 2019
$570k
NIDDK NIH HHS K01 DK109027NIDDK NIH HHS K01 DK111771NIDDK NIH HHS R01 DK064261NIDDK NIH HHS R01 DK066556NIDDK NIH HHS R01 DK088220
6 · The paper itself

Abstract

Adipose progenitor cells (APCs) reside in a vascular niche, located within the perivascular compartment of adipose tissue blood vessels. Yet, the signals and mechanisms that govern adipose vascular niche formation and APC niche interaction are unknown. Here we show that the assembly and maintenance of the adipose vascular niche is controlled by PPARγ acting within APCs. PPARγ triggers a molecular hierarchy that induces vascular sprouting, APC vessel niche affinity and APC vessel occupancy. Mechanistically, PPARγ transcriptionally activates PDGFRβ and VEGF. APC expression and activation of PDGFRβ promotes the recruitment and retention of APCs to the niche. Pharmacologically, targeting PDGFRβ disrupts APC niche contact thus blocking adipose tissue expansion. Moreover, enhanced APC expression of VEGF stimulates endothelial cell proliferation and expands the adipose niche. Consequently, APC niche communication and retention are boosted by VEGF thereby impairing adipogenesis. Our data indicate that APCs direct adipose tissue niche expansion via a PPARγ-initiated PDGFRβ and VEGF transcriptional axis.

Indexed as

Stem Cell NicheAdipocytesAdipogenesisAdipose TissueAnimalsCell ProliferationFemaleMaleMicePPAR gammaReceptor, Platelet-Derived Growth Factor betaStem CellsVascular Endothelial Growth Factor APPAR gammaReceptor, Platelet-Derived Growth Factor betaVascular Endothelial Growth Factor A

Identifiers

PMID28649987
PMCPMC5490270
OpenAlexW2689157790

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.