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Bioactive lipid mediator class switching regulates myogenic cell progression and muscle regeneration

Author

Listed:
  • Paul Fabre

    (CHU Sainte-Justine Research Center
    Université de Montréal)

  • Thomas Molina

    (CHU Sainte-Justine Research Center
    Université de Montréal)

  • Jessica Larose

    (CHU de Québec-Laval University Research Center)

  • Karine Greffard

    (CHU de Québec-Laval University Research Center)

  • Gregory Généreux-Gamache

    (CHU Sainte-Justine Research Center
    Université de Montréal)

  • Alyson Deprez

    (CHU Sainte-Justine Research Center
    Université de Montréal)

  • Inès Mokhtari

    (CHU Sainte-Justine Research Center
    Université de Montréal)

  • Ornella Pellerito

    (CHU Sainte-Justine Research Center)

  • Elise Duchesne

    (Université Laval
    CHU de Québec - Université Laval Research Center
    Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay-Lac-Saint-Jean
    Centre Intégré Universitaire de Santé et de Services Sociaux Capitale-Nationale)

  • Junio Dort

    (University of Ottawa)

  • Jean-François Bilodeau

    (CHU de Québec-Laval University Research Center
    Université Laval)

  • Nicolas A. Dumont

    (CHU Sainte-Justine Research Center
    Université de Montréal)

Abstract

The muscle stem cell niche is well-described as influencing myogenic cell fate decision; however, the intrinsic mechanisms driving muscle stem cell progression during myogenesis are not yet fully elucidated. Here, we demonstrate that bioactive lipid class switching, an auto-regulatory mechanism originally described during the inflammatory process, is conserved during myogenesis. During the transition from proliferation to differentiation, myogenic cells shift from pro-inflammatory to pro-resolution pathways, a process partially mediated by 15Δ-PGJ2 that promotes the expression of the prostaglandin inactivation enzyme 15-hydroxyprostaglandin dehydrogenase. Using pharmacological inhibitors and knockout models of the pro-resolution enzyme 15-lipoxygenase, we show that blocking the bioactive lipid class switching impairs myoblast differentiation in vitro and muscle regeneration in vivo. Administration of the pro-resolving mediator Protectin-D1 restores myogenesis, enhances muscle regeneration post-injury and improves muscle phenotype in a dystrophic mouse model. Overall, these findings provide a better comprehension of the mechanisms regulating myogenic progression, which opens new therapeutic avenues for muscle regeneration and dystrophies.

Suggested Citation

  • Paul Fabre & Thomas Molina & Jessica Larose & Karine Greffard & Gregory Généreux-Gamache & Alyson Deprez & Inès Mokhtari & Ornella Pellerito & Elise Duchesne & Junio Dort & Jean-François Bilodeau & Ni, 2025. "Bioactive lipid mediator class switching regulates myogenic cell progression and muscle regeneration," Nature Communications, Nature, vol. 16(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-60586-8
    DOI: 10.1038/s41467-025-60586-8
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    References listed on IDEAS

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    1. Paraskevi Krashia & Alberto Cordella & Annalisa Nobili & Livia Barbera & Mauro Federici & Alessandro Leuti & Federica Campanelli & Giuseppina Natale & Gioia Marino & Valeria Calabrese & Francescangelo, 2019. "Author Correction: Blunting neuroinflammation with resolvin D1 prevents early pathology in a rat model of Parkinson’s disease," Nature Communications, Nature, vol. 10(1), pages 1-1, December.
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    5. Talita C. Conte & Gilberto Duran-Bishop & Zakaria Orfi & Inès Mokhtari & Alyson Deprez & Isabelle Côté & Thomas Molina & Tae-Yeon Kim & Lydia Tellier & Marie-Pier Roussel & Damien Maggiorani & Basma B, 2023. "Clearance of defective muscle stem cells by senolytics restores myogenesis in myotonic dystrophy type 1," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    6. Junio Dort & Zakaria Orfi & Paul Fabre & Thomas Molina & Talita C. Conte & Karine Greffard & Ornella Pellerito & Jean-François Bilodeau & Nicolas A. Dumont, 2021. "Resolvin-D2 targets myogenic cells and improves muscle regeneration in Duchenne muscular dystrophy," Nature Communications, Nature, vol. 12(1), pages 1-17, December.
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