Fabre Paul, Molina Thomas, Larose Jessica, Greffard Karine, Généreux-Gamache Gregory, Deprez Alyson, Mokhtari Inès, Pellerito Ornella, Duchesne Elise, Dort Junio, Bilodeau Jean-François, Dumont Nicolas A
CHU Sainte-Justine Research Center, Montreal, QC, Canada.
Department of pharmacology and physiology, Faculty of Medicine, Université de Montréal, Montréal, QC, Canada.
Nat Commun. 2025 Jul 1;16(1):5578. doi: 10.1038/s41467-025-60586-8.
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-PGJ 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.
肌肉干细胞微环境被充分描述为影响成肌细胞命运决定;然而,在肌生成过程中驱动肌肉干细胞进展的内在机制尚未完全阐明。在这里,我们证明生物活性脂质类别转换,一种最初在炎症过程中描述的自我调节机制,在肌生成过程中是保守的。在从增殖向分化的转变过程中,成肌细胞从促炎途径转变为促消退途径,这一过程部分由促进前列腺素失活酶15-羟基前列腺素脱氢酶表达的15Δ-PGJ介导。使用促消退酶15-脂氧合酶的药理抑制剂和基因敲除模型,我们表明阻断生物活性脂质类别转换会损害体外成肌细胞分化和体内肌肉再生。给予促消退介质保护素-D1可恢复肌生成,增强损伤后肌肉再生,并改善营养不良小鼠模型中的肌肉表型。总体而言,这些发现更好地理解了调节肌生成进展的机制,为肌肉再生和肌营养不良症开辟了新的治疗途径。