Evidence map›Paper›PMID 31767614›Full record

ArticleLife science alliance2019

Refining the adipose progenitor cell landscape in healthy and obese visceral adipose tissue using single-cell gene expression profiling.

Dong Seong Cho, Bolim Lee, Jason D Doles

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

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  12. [Research progress in regulation of hair growth by dermal adipose tissue].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2024
    Review
  13. Whole-Mount Imaging of Adipose Tissue Macrophages.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
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  16. Aging and obesity prime the methylome and transcriptome of adipose stem cells for disease and dysfunction.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
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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

3 authors at 1 institution in 1 country.

Dong Seong ChoDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Bolim LeeDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Jason D DolesDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA Doles.Jason@mayo.edu.ORCID 0000-0002-6830-708X
Mayo Clinic in Arizona · US

Funding

Mechanisms of sepsis-associated muscle stem cell dysfunctionR35GM128594 · NIGMS · MAYO CLINIC ROCHESTER · PI DOLES, JASON · 2018 to 2022
$2.0M
Post-transcriptional Regulation of Satellite Cell FunctionR00AR066696 · NIAMS · MAYO CLINIC ROCHESTER · PI DOLES, JASON · 2016 to 2018
$961k
Post-transcriptional Regulation of Satellite Cell FunctionK99AR066696 · NIAMS · UNIVERSITY OF COLORADO · PI DOLES, JASON · 2015 to 2015
$93k
NIAMS NIH HHS K99 AR066696NIAMS NIH HHS R00 AR066696NIGMS NIH HHS R35 GM128594
6 · The paper itself

Abstract

Obesity is a serious health concern and is associated with a reduced quality of life and a number of chronic diseases, including diabetes, heart disease, stroke, and cancer. With obesity rates on the rise worldwide, adipose tissue biology has become a top biomedical research priority. Despite steady growth in obesity-related research, more investigation into the basic biology of adipose tissue is needed to drive innovative solutions aiming to curtail the obesity epidemic. Adipose progenitor cells (APCs) play a central role in adipose tissue homeostasis and coordinate adipose tissue expansion and remodeling. Although APCs are well studied, defining and characterizing APC subsets remains ambiguous because of ill-defined cellular heterogeneity within this cellular compartment. In this study, we used single-cell RNA sequencing to create a cellular atlas of APC heterogeneity in mouse visceral adipose tissue. Our analysis identified two distinct populations of adipose tissue-derived stem cells (ASCs) and three distinct populations of preadipocytes (PAs). We identified novel cell surface markers that, when used in combination with traditional ASC and preadipocyte markers, could discriminate between these APC subpopulations by flow cytometry. Prospective isolation and molecular characterization of these APC subpopulations confirmed single-cell RNA sequencing gene expression signatures, and ex vivo culture revealed differential expansion/differentiation capabilities. Obese visceral adipose tissue featured relative expansion of less mature ASC and PA subpopulations, and expression analyses revealed major obesity-associated signaling alterations within each APC subpopulation. Taken together, our study highlights cellular and transcriptional heterogeneity within the APC pool, provides new tools to prospectively isolate and study these novel subpopulations, and underscores the importance of considering APC diversity when studying the etiology of obesity.

Indexed as

AdipocytesAdipogenesisAdipose TissueAnimalsCell DifferentiationFlow CytometryGene Expression ProfilingIntra-Abdominal FatMaleMiceMice, Inbred StrainsObesitySingle-Cell AnalysisStem CellsSubcutaneous FatTissue Array Analysis

Identifiers

PMID31767614
PMCPMC6878222
OpenAlexW2989974113

What OpenQuestion holds

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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.