Intramuscular IL-10 Administration Enhances the Activity of Myogenic Precursor Cells and Improves Motor Function in ALS Mouse Model.
Paola FabbrizioCassandra MargottaJessica D'AgostinoGiuseppe SuannoLorenzo QuettiCaterina BendottiGiovanni NardoPublished in: Cells (2023)
Amyotrophic Lateral Sclerosis (ALS) is the most common adult motor neuron disease, with a poor prognosis, a highly unmet therapeutic need, and a burden on health care costs. Hitherto, strategies aimed at protecting motor neurons have missed or modestly delayed ALS due to a failure in countering the irreversible muscular atrophy. We recently provided direct evidence underlying the pivotal role of macrophages in preserving skeletal muscle mass. Based on these results, we explored whether the modulation of macrophage muscle response and the enhancement of satellite cell differentiation could effectively promote the generation of new myofibers and counteract muscle dysfunction in ALS mice. For this purpose, disease progression and the survival of SOD1G93A mice were evaluated following IL-10 injections in the hindlimb skeletal muscles. Thereafter, we used ex vivo methodologies and in vitro approaches on primary cells to assess the effect of the treatment on the main pathological signatures. We found that IL-10 improved the motor performance of ALS mice by enhancing satellite cells and the muscle pro-regenerative activity of macrophages. This resulted in delayed muscle atrophy and motor neuron loss. Our findings provide the basis for a suitable adjunct multisystem therapeutic approach that pinpoints a primary role of muscle pathology in ALS.
Keyphrases
- amyotrophic lateral sclerosis
- induced apoptosis
- skeletal muscle
- poor prognosis
- cell cycle arrest
- mouse model
- healthcare
- stem cells
- high fat diet induced
- dna methylation
- cell death
- genome wide
- mesenchymal stem cells
- adipose tissue
- signaling pathway
- wild type
- young adults
- anti inflammatory
- gene expression
- social media
- smoking cessation
- childhood cancer