Evidence map›Paper›PMID 30054310›Full record

ArticleJournal of cell science2018

Distinct metabolic states govern skeletal muscle stem cell fates during prenatal and postnatal myogenesis.

Francesca Pala, Daniela Di Girolamo, Sébastien Mella, Siham Yennek, Laurent Chatre, Miria Ricchetti, Shahragim Tajbakhsh

Abstract read
In one paragraph

Article in Journal of cell science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed
–field-weighted citation impact
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

103 citing papers in PubMed.

  1. Elevated mitochondrial CaStem cell reports · 2026
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43 more citing papers are in PubMed but not listed here.

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

7 authors.

Francesca PalaStem Cells and Development, Department of Developmental & Stem Cell Biology, Institut Pasteur, Paris 75015, France.
Daniela Di GirolamoStem Cells and Development, Department of Developmental & Stem Cell Biology, Institut Pasteur, Paris 75015, France.ORCID 0000-0001-5746-9211
Sébastien MellaStem Cells and Development, Department of Developmental & Stem Cell Biology, Institut Pasteur, Paris 75015, France.
Siham YennekStem Cells and Development, Department of Developmental & Stem Cell Biology, Institut Pasteur, Paris 75015, France.
Laurent ChatreCNRS UMR 3738, Institut Pasteur, Paris 75015, France.
Miria RicchettiCNRS UMR 3738, Institut Pasteur, Paris 75015, France.
Shahragim TajbakhshStem Cells and Development, Department of Developmental & Stem Cell Biology, Institut Pasteur, Paris 75015, France shahragim.tajbakhsh@pasteur.fr.ORCID 0000-0003-1809-7202

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During growth, homeostasis and regeneration, stem cells are exposed to different energy demands. Here, we characterise the metabolic pathways that mediate the commitment and differentiation of mouse skeletal muscle stem cells, and how their modulation can influence the cell state. We show that quiescent satellite stem cells have low energetic demands and perturbed oxidative phosphorylation during ageing, which is also the case for cells from post-mortem tissues. We show also that myogenic fetal cells have distinct metabolic requirements compared to those proliferating during regeneration, with the former displaying a low respiration demand relying mostly on glycolysis. Furthermore, we show distinct requirements for peroxisomal and mitochondrial fatty acid oxidation (FAO) in myogenic cells. Compromising peroxisomal but not mitochondrial FAO promotes early differentiation of myogenic cells. Acute muscle injury and pharmacological block of peroxisomal and mitochondrial FAO expose differential requirements for these organelles during muscle regeneration. Taken together, these observations indicate that changes in myogenic cell state lead to significant alterations in metabolic requirements. In addition, perturbing specific metabolic pathways impacts on myogenic cell fates and the regeneration process.

Indexed as

Muscle DevelopmentAnimalsCell ProliferationFatty AcidsMiceMitochondriaMuscle, SkeletalOxidation-ReductionPeroxisomesSatellite Cells, Skeletal MuscleStem CellsFatty AcidsAgeingMetabolic stateMitochondriaPeroxisomeRegenerationSkeletal muscle stem cells

Identifiers

PMID30054310
PMCPMC6080609

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Registered trials

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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.