Macrophages fine tune satellite cell fate in dystrophic skeletal muscle of mdx mice.
Luca MadaroAlessio TorcinaroMarco De BardiFederica F ContinoMattia PelizzolaGiuseppe Riccardo DiaferiaGiulia ImeneoMarina BouchèPier Lorenzo PuriFrancesca De SantaPublished in: PLoS genetics (2019)
Satellite cells (SCs) are muscle stem cells that remain quiescent during homeostasis and are activated in response to acute muscle damage or in chronic degenerative conditions such as Duchenne Muscular Dystrophy. The activity of SCs is supported by specialized cells which either reside in the muscle or are recruited in regenerating skeletal muscles, such as for instance macrophages (MΦs). By using a dystrophic mouse model of transient MΦ depletion, we describe a shift in identity of muscle stem cells dependent on the crosstalk between MΦs and SCs. Indeed MΦ depletion determines adipogenic conversion of SCs and exhaustion of the SC pool leading to an exacerbated dystrophic phenotype. The reported data could also provide new insights into therapeutic approaches targeting inflammation in dystrophic muscles.
Keyphrases
- skeletal muscle
- stem cells
- duchenne muscular dystrophy
- induced apoptosis
- oxidative stress
- cell cycle arrest
- mouse model
- cell fate
- insulin resistance
- endoplasmic reticulum stress
- palliative care
- cell therapy
- intensive care unit
- electronic health record
- signaling pathway
- mesenchymal stem cells
- machine learning
- type diabetes
- hepatitis b virus
- high fat diet induced
- cancer therapy
- cell proliferation
- pi k akt
- cerebral ischemia
- blood brain barrier
- aortic dissection
- acute respiratory distress syndrome