Evidence map›Paper›PMID 28992793›Full record

ArticleStem cells and development2017

The Short-Chain Fatty Acid Propionate Inhibits Adipogenic Differentiation of Human Chorion-Derived Mesenchymal Stem Cells Through the Free Fatty Acid Receptor 2.

Judit Iván, Evelin Major, Adrienn Sipos, Katalin Kovács, Dániel Horváth, István Tamás, Péter Bay, Viktor Dombrádi, Beáta Lontay

Open access · hybridAbstract read
In one paragraph

Article in Stem cells and development, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 59 citations in OpenAlex.

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  5. Propionate Induces Energy Expenditure via Browning in Mesenteric Adipose Tissue.The Journal of clinical endocrinology and metabolism · 2025
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  15. Short-Chain Fatty Acid Receptors and Cardiovascular Function.International journal of molecular sciences · 2022
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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

9 authors at 1 institution in 2 countries.

Judit Iván1 Department of Medical Chemistry, Faculty of Medicine, University of Debrecen , Debrecen, Hungary .
Evelin Major1 Department of Medical Chemistry, Faculty of Medicine, University of Debrecen , Debrecen, Hungary .
Adrienn Sipos1 Department of Medical Chemistry, Faculty of Medicine, University of Debrecen , Debrecen, Hungary .
Katalin Kovács1 Department of Medical Chemistry, Faculty of Medicine, University of Debrecen , Debrecen, Hungary .
Dániel Horváth1 Department of Medical Chemistry, Faculty of Medicine, University of Debrecen , Debrecen, Hungary .
István Tamás1 Department of Medical Chemistry, Faculty of Medicine, University of Debrecen , Debrecen, Hungary .
Péter Bay1 Department of Medical Chemistry, Faculty of Medicine, University of Debrecen , Debrecen, Hungary .
Viktor Dombrádi1 Department of Medical Chemistry, Faculty of Medicine, University of Debrecen , Debrecen, Hungary .
Beáta Lontay1 Department of Medical Chemistry, Faculty of Medicine, University of Debrecen , Debrecen, Hungary .
University of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Free fatty acid receptor 2 (FFAR2, also known as GPR43) is a G-protein-coupled receptor activated by short-chain fatty acids that are produced by gut microbiota through fermentation of nondigestible carbohydrates. FFAR2 functions as a metabolic sensor and is expressed in metabolically active tissues, such as adipose tissue. Earlier studies proved the connection between FFAR2 and adipocyte differentiation in mice. The aim of this study was to investigate the implication of FFAR2 receptor in adipogenesis in human chorion-derived mesenchymal stem cells (cMSCs). The short-chain fatty acid, propionate, and phenylacetamide a selective FFAR2 agonist resulted in a marked suppression of lipid droplet accumulation during the adipogenic differentiation of cMSCs. Western blot studies revealed that FFAR2 was detectable at any time point of the differentiation period. The direct involvement of FFAR2 in the differentiation into adipocytes was proven by the downregulation of its gene expression in cMSCs by lentiviral messenger RNA (mRNA) silencing transduction particles. Our results showed that a significant suppression in lipid accumulation upon FFAR2 agonist treatments was elicited by FFAR2-silencing. Based on these results we suggest that propionate inhibits the formation of adipocytes from MSCs and acts on adipogenesis predominantly via FFAR2.

Indexed as

Cell DifferentiationAdipocytesCells, CulturedChorionHumansLipid DropletsMesenchymal Stem CellsPropionatesReceptors, Cell SurfaceReceptors, G-Protein-CoupledFFAR2 protein, humanPropionatesReceptors, Cell SurfaceReceptors, G-Protein-Coupledadipose tissue differentiationcMSCFFAR2 (GPR43)free fatty acids

Identifiers

PMID28992793
PMCPMC5706617
OpenAlexW2764311734

What OpenQuestion holds

Textmetadata
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.