Evidence map›Paper›PMID 25505127›Full record

ArticleMolecular & cellular proteomics : MCP2015

A proteomic analysis reveals that Snail regulates the expression of the nuclear orphan receptor Nuclear Receptor Subfamily 2 Group F Member 6 (Nr2f6) and interleukin 17 (IL-17) to inhibit adipocyte differentiation.

Alberto Peláez-García, Rodrigo Barderas, Raquel Batlle, Rosa Viñas-Castells, Rubén A Bartolomé, Sofía Torres, Marta Mendes, María Lopez-Lucendo, Rocco Mazzolini, Félix Bonilla and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 42 citations in OpenAlex.

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  12. Proteomic andFrontiers in microbiology · 2022
    Article
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  15. Article
  16. Article
  17. The emerging role of Snail1 in the tumor stroma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2016
    Review
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  19. Article
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

12 authors at 4 institutions in 1 country.

Alberto Peláez-GarcíaFrom the ‡Department of Cellular and Molecular Medicine, Centro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain;
Rodrigo Barderas§Departamento de Biochemistry and Molecular Biology Department I, Universidad Complutense de Madrid, Spain;
Raquel Batlle¶IMIM-Hospital del Mar. Barcelona, Spain;
Rosa Viñas-Castells¶IMIM-Hospital del Mar. Barcelona, Spain;
Rubén A BartoloméFrom the ‡Department of Cellular and Molecular Medicine, Centro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain;
Sofía TorresFrom the ‡Department of Cellular and Molecular Medicine, Centro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain;
Marta MendesFrom the ‡Department of Cellular and Molecular Medicine, Centro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain;
María Lopez-LucendoFrom the ‡Department of Cellular and Molecular Medicine, Centro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain;
Rocco Mazzolini¶IMIM-Hospital del Mar. Barcelona, Spain;
Félix Bonilla‖Hospital Puerta de Hierro, Majadahonda, Madrid, Spain.
Antonio García de Herreros¶IMIM-Hospital del Mar. Barcelona, Spain;
J Ignacio CasalFrom the ‡Department of Cellular and Molecular Medicine, Centro de Investigaciones Biológicas (CIB-CSIC), Madrid, Spain; icasal@cib.csic.es.
Centro de Investigaciones Biológicas Margarita Salas · ESHospital Del Mar · ESHospital Universitario Puerta de Hierro Majadahonda · ESUniversidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adipogenesis requires a differentiation program driven by multiple transcription factors, where PPARγ and C/EBPα play a central role. Recent findings indicate that Snail inhibits adipocyte differentiation in 3T3-L1 and murine mesenchymal stem cells (mMSC). An in-depth quantitative SILAC analysis of the nuclear fraction of Snail-induced alterations of 3T3-L1 cells was carried out. In total, 2251 overlapping proteins were simultaneously quantified in forward and reverse experiments. We observed 574 proteins deregulated by Snail1 using a fold-change ≥1.5, with 111 up- and 463 down-regulated proteins, respectively. Among other proteins, multiple transcription factors such as Trip4, OsmR, Nr2f6, Cbx6, and Prrx1 were down-regulated. Results were validated in 3T3-L1 cells and mMSC cells by Western blot and quantitative PCR. Knock-down experiments in 3T3-L1 cells demonstrated that only Nr2f6 (and Trip4 at minor extent) was required for adipocyte differentiation. Ectopic expression of Nr2f6 reversed the effects of Snail1 and promoted adipogenesis. Because Nr2f6 inhibits the expression of IL-17, we tested the effect of Snail on IL-17 expression. IL-17 and TNFα were among the most up-regulated pro-inflammatory cytokines in Snail-transfected 3T3-L1 and mMSC cells. Furthermore, the blocking of IL-17 activity in Snail-transfected cells promoted adipocyte differentiation, reverting Snail inhibition. In summary, Snail inhibits adipogenesis through a down-regulation of Nr2f6, which in turn facilitates the expression of IL-17, an anti-adipogenic cytokine. These results would support a novel and important role for Snail and Nr2f6 in obesity control.

Indexed as

Cell Differentiation3T3-L1 CellsAdipocytesAdipogenesisAnimalsCell ExtractsCell NucleusCOUP Transcription FactorsDown-RegulationInterleukin-17Mesenchymal Stem CellsMiceModels, BiologicalProteomicsRepressor ProteinsReproducibility of ResultsCell ExtractsCOUP Transcription FactorsInterleukin-17Nr2f6 protein, mouseRepressor ProteinsSnai1 protein, mouseSnail Family Transcription FactorsTranscription Factors

Identifiers

PMID25505127
PMCPMC4350027
OpenAlexW2186367624

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.