Evidence map›Paper›PMID 34440643›Full record

ArticleCells2021

Concurrent BMP Signaling Maintenance and TGF-β Signaling Inhibition Is a Hallmark of Natural Resistance to Muscle Atrophy in the Hibernating Bear.

Laura Cussonneau, Christian Boyer, Charlotte Brun, Christiane Deval, Emmanuelle Loizon, Emmanuelle Meugnier, Elise Gueret, Emeric Dubois, Daniel Taillandier, Cécile Polge and 10 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 20 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

20 authors at 7 institutions in 3 countries.

Laura CussonneauINRAE, Unité de Nutrition Humaine, Université Clermont Auvergne, UMR 1019, F-63000 Clermont-Ferrand, France.ORCID 0000-0002-3017-2685
Christian BoyerINRAE, Unité de Nutrition Humaine, Université Clermont Auvergne, UMR 1019, F-63000 Clermont-Ferrand, France.
Charlotte BrunUniversité de Strasbourg, CNRS, IPHC UMR 7178, F-67000 Strasbourg, France.
Christiane DevalINRAE, Unité de Nutrition Humaine, Université Clermont Auvergne, UMR 1019, F-63000 Clermont-Ferrand, France.
Emmanuelle LoizonCarMen Laboratory, INSERM 1060, INRAE 1397, University of Lyon, F-69600 Oullins, France.
Emmanuelle MeugnierCarMen Laboratory, INSERM 1060, INRAE 1397, University of Lyon, F-69600 Oullins, France.
Elise GueretInstitut de Génomique Fonctionnelle (IGF), University Montpellier, CNRS, INSERM, 34094 Montpellier, France.ORCID 0000-0003-0714-3197
Emeric DuboisInstitut de Génomique Fonctionnelle (IGF), University Montpellier, CNRS, INSERM, 34094 Montpellier, France.ORCID 0000-0002-6052-4178
Daniel TaillandierINRAE, Unité de Nutrition Humaine, Université Clermont Auvergne, UMR 1019, F-63000 Clermont-Ferrand, France.
Cécile PolgeINRAE, Unité de Nutrition Humaine, Université Clermont Auvergne, UMR 1019, F-63000 Clermont-Ferrand, France.ORCID 0000-0002-8730-5776
Daniel BéchetINRAE, Unité de Nutrition Humaine, Université Clermont Auvergne, UMR 1019, F-63000 Clermont-Ferrand, France.ORCID 0000-0002-3812-8099
Guillemette Gauquelin-KochCentre National d'Etudes Spatiales, CNES, 75001 Paris, France.
Alina L EvansDepartment of Forestry and Wildlife Management, Inland Norway University of Applied Sciences, Campus Evenstad, NO-2480 Koppang, Norway.
Jon M ArnemoDepartment of Forestry and Wildlife Management, Inland Norway University of Applied Sciences, Campus Evenstad, NO-2480 Koppang, Norway.
Jon E SwensonFaculty of Environmental Sciences and Natural Resource Management, Norwegian University of Life Sciences, NO-1432 Ås, Norway.
Stéphane BlancUniversité de Strasbourg, CNRS, IPHC UMR 7178, F-67000 Strasbourg, France.
Chantal SimonCarMen Laboratory, INSERM 1060, INRAE 1397, University of Lyon, F-69600 Oullins, France.ORCID 0000-0002-7820-3233
Etienne LefaiINRAE, Unité de Nutrition Humaine, Université Clermont Auvergne, UMR 1019, F-63000 Clermont-Ferrand, France.ORCID 0000-0002-3042-7801
Fabrice BertileUniversité de Strasbourg, CNRS, IPHC UMR 7178, F-67000 Strasbourg, France.ORCID 0000-0001-5510-4868
Lydie CombaretINRAE, Unité de Nutrition Humaine, Université Clermont Auvergne, UMR 1019, F-63000 Clermont-Ferrand, France.ORCID 0000-0001-6550-8700
Université Clermont Auvergne · FRCentre National de la Recherche Scientifique · FRUniversité Claude Bernard Lyon 1 · FRCentre National d'Études Spatiales · FRNorwegian University of Life Sciences · NOSwedish University of Agricultural Sciences · SEUniversity of Inland Norway · NO

Funding

Agence Nationale de la Recherche ANR-10-INBS-09Centre National d'Etudes Spatiales 1006Centre National d'Etudes Spatiales 1905Centre National d'Etudes Spatiales 865Centre National d'Etudes Spatiales 974Clermont Auvergne Metropole, INRAE 23001142iSITE Challenge 3 Mobility Program IR18LEFAI
6 · The paper itself

Abstract

Muscle atrophy arises from a multiplicity of physio-pathological situations and has very detrimental consequences for the whole body. Although knowledge of muscle atrophy mechanisms keeps growing, there is still no proven treatment to date. This study aimed at identifying new drivers for muscle atrophy resistance. We selected an innovative approach that compares muscle transcriptome between an original model of natural resistance to muscle atrophy, the hibernating brown bear, and a classical model of induced atrophy, the unloaded mouse. Using RNA sequencing, we identified 4415 differentially expressed genes, including 1746 up- and 2369 down-regulated genes, in bear muscles between the active versus hibernating period. We focused on the Transforming Growth Factor (TGF)-β and the Bone Morphogenetic Protein (BMP) pathways, respectively, involved in muscle mass loss and maintenance. TGF-β- and BMP-related genes were overall down- and up-regulated in the non-atrophied muscles of the hibernating bear, respectively, and the opposite occurred for the atrophied muscles of the unloaded mouse. This was further substantiated at the protein level. Our data suggest TGF-β/BMP balance is crucial for muscle mass maintenance during long-term physical inactivity in the hibernating bear. Thus, concurrent activation of the BMP pathway may potentiate TGF-β inhibiting therapies already targeted to prevent muscle atrophy.

Indexed as

HibernationAnimalsBone Morphogenetic ProteinsDisease Models, AnimalFemaleGene Expression ProfilingGene Expression RegulationGene Regulatory NetworksHindlimb SuspensionMaleMiceMice, Inbred C57BLMuscular AtrophyQuadriceps MuscleRNA-SeqSignal TransductionBone Morphogenetic ProteinsTransforming Growth Factor betabrown bear hibernationmouse unloadingmuscle atrophyphysical inactivityRNA sequencingTGF-β/BMP signaling

Identifiers

PMID34440643
PMCPMC8393865
OpenAlexW3185119031

What Socratic 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 Socratic graph.