Metabolic reprogramming of fibro/adipogenic progenitors facilitates muscle regeneration.
Alessio ReggioMarco RosinaNatalie KrahmerAlessandro PalmaLucia Lisa PetrilliGiuliano MaiolatesiGiorgia MassacciIllari SalvatoriCristiana ValleStefano TestaCesare GargioliClaudia FuocoLuisa CastagnoliGianni CesareniFrancesca SaccoPublished in: Life science alliance (2020)
In Duchenne muscular dystrophy (DMD), the absence of the dystrophin protein causes a variety of poorly understood secondary effects. Notably, muscle fibers of dystrophic individuals are characterized by mitochondrial dysfunctions, as revealed by a reduced ATP production rate and by defective oxidative phosphorylation. Here, we show that in a mouse model of DMD (mdx), fibro/adipogenic progenitors (FAPs) are characterized by a dysfunctional mitochondrial metabolism which correlates with increased adipogenic potential. Using high-sensitivity mass spectrometry-based proteomics, we report that a short-term high-fat diet (HFD) reprograms dystrophic FAP metabolism in vivo. By combining our proteomic dataset with a literature-derived signaling network, we revealed that HFD modulates the β-catenin-follistatin axis. These changes are accompanied by significant amelioration of the histological phenotype in dystrophic mice. Transplantation of purified FAPs from HFD-fed mice into the muscles of dystrophic recipients demonstrates that modulation of FAP metabolism can be functional to ameliorate the dystrophic phenotype. Our study supports metabolic reprogramming of muscle interstitial progenitor cells as a novel approach to alleviate some of the adverse outcomes of DMD.
Keyphrases
- duchenne muscular dystrophy
- high fat diet
- insulin resistance
- mass spectrometry
- adipose tissue
- skeletal muscle
- high fat diet induced
- mouse model
- muscular dystrophy
- oxidative stress
- stem cells
- systematic review
- liquid chromatography
- high resolution
- epithelial mesenchymal transition
- type diabetes
- label free
- high performance liquid chromatography
- mesenchymal stem cells
- bone marrow
- capillary electrophoresis
- wound healing