Evidence map›Paper›PMID 27010359›Full record

ArticleScientific reports2016

Hedgehog associated to microparticles inhibits adipocyte differentiation via a non-canonical pathway.

Audrey Fleury, Lucile Hoch, M Carmen Martinez, Hélène Faure, Maurizio Taddei, Elena Petricci, Fabrizio Manetti, Nicolas Girard, André Mann, Caroline Jacques and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.1field-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

16 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  9. Review
  10. The hedgehog pathway in nonalcoholic fatty liver disease.Critical reviews in biochemistry and molecular biology · 2018
    Review
  11. Emerging nonmetabolic functions of skin fat.Nature reviews. Endocrinology · 2018
    Review
  12. Article
  13. Article
  14. Article
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  16. 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

14 authors at 6 institutions in 2 countries.

Audrey FleuryINSERM U1063, Université d'Angers, IBS-IRIS Rue des Capucins, F-49100 Angers, France.
Lucile HochCNRS, UMR-9197, Neuroscience Paris-Saclay Institute, Molecules Circuits Department, 1 Avenue de la Terrasse, F-91198, Gif sur Yvette, France.
M Carmen MartinezINSERM U1063, Université d'Angers, IBS-IRIS Rue des Capucins, F-49100 Angers, France.
Hélène FaureCNRS, UMR-9197, Neuroscience Paris-Saclay Institute, Molecules Circuits Department, 1 Avenue de la Terrasse, F-91198, Gif sur Yvette, France.
Maurizio TaddeiDipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via A. Moro 2, I-53100, Siena, Italy.
Elena PetricciDipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via A. Moro 2, I-53100, Siena, Italy.
Fabrizio ManettiDipartimento di Biotecnologie, Chimica e Farmacia, Università degli Studi di Siena, Via A. Moro 2, I-53100, Siena, Italy.
Nicolas GirardCNRS, UMR-7200, Laboratoire d'Innovation Thérapeutique, Université de Strasbourg, 74 Route du Rhin, BP 60024, F-67401 Illkirch, France.
André MannCNRS, UMR-7200, Laboratoire d'Innovation Thérapeutique, Université de Strasbourg, 74 Route du Rhin, BP 60024, F-67401 Illkirch, France.
Caroline JacquesINSERM U1063, Université d'Angers, IBS-IRIS Rue des Capucins, F-49100 Angers, France.
Jérôme LargheroAssistance Publique - Hôpitaux de Paris, Hôpital Saint-Louis, Unité de Thérapie Cellulaire; Inserm UMR1160 et CIC de Biothérapies; Univ Paris Diderot, Sorbonne Paris Cité, F-75475, Paris, France.
Martial RuatCNRS, UMR-9197, Neuroscience Paris-Saclay Institute, Molecules Circuits Department, 1 Avenue de la Terrasse, F-91198, Gif sur Yvette, France.
Ramaroson AndriantsitohainaINSERM U1063, Université d'Angers, IBS-IRIS Rue des Capucins, F-49100 Angers, France.
Soazig Le LayINSERM U1063, Université d'Angers, IBS-IRIS Rue des Capucins, F-49100 Angers, France.
Laboratoire Stress Oxydant et Pathologies Métaboliques · FRUniversity of Siena · ITLaboratoire d'Innovation Thérapeutique · FRUniversité Paris-Sud · FRAssistance Publique – Hôpitaux de Paris · FRInstitut des Neurosciences Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hedgehog (Hh) is a critical regulator of adipogenesis. Extracellular vesicles are natural Hh carriers, as illustrated by activated/apoptotic lymphocytes specifically shedding microparticles (MP) bearing the morphogen (MP(Hh+)). We show that MP(Hh+) inhibit adipocyte differentiation and orientate mesenchymal stem cells towards a pro-osteogenic program. Despite a Smoothened (Smo)-dependency, MP(Hh+) anti-adipogenic effects do not activate a canonical Hh signalling pathway in contrast to those elicited either by the Smo agonist SAG or recombinant Sonic Hedgehog. The Smo agonist GSA-10 recapitulates many of the hallmarks of MP(Hh+) anti-adipogenic effects. The adipogenesis blockade induced by MP(Hh+) and GSA-10 was abolished by the Smo antagonist LDE225. We further elucidate a Smo/Lkb1/Ampk axis as the non-canonical Hh pathway used by MP(Hh+) and GSA-10 to inhibit adipocyte differentiation. Our results highlight for the first time the ability of Hh-enriched MP to signal via a non-canonical pathway opening new perspectives to modulate fat development.

Indexed as

3T3-L1 CellsAdipocytesAnimalsCell DifferentiationCells, CulturedHedgehog ProteinsHumansMesenchymal Stem CellsMiceTranscription FactorsHedgehog ProteinsTranscription Factors

Identifiers

PMID27010359
PMCPMC4806302
OpenAlexW2332785941

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.