Mast cells and neutrophils mediate peripheral motor pathway degeneration in ALS

Neuroinflammation is a recognized pathogenic mechanism underlying motor neuron degeneration in amyotrophic lateral sclerosis (ALS), but the inflammatory mechanisms influencing peripheral motor axon degeneration remain largely unknown. A recent report showed a pathogenic role for c-Kit-expressing mas...

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Published inJCI insight Vol. 3; no. 19
Main Authors Trias, Emiliano, King, Peter H., Si, Ying, Kwon, Yuri, Varela, Valentina, Ibarburu, Sofía, Kovacs, Mariángeles, Moura, Ivan C., Beckman, Joseph S., Hermine, Olivier, Barbeito, Luis
Format Journal Article
LanguageEnglish
Published United States American Society for Clinical Investigation 04.10.2018
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ISSN2379-3708
2379-3708
DOI10.1172/jci.insight.123249

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Summary:Neuroinflammation is a recognized pathogenic mechanism underlying motor neuron degeneration in amyotrophic lateral sclerosis (ALS), but the inflammatory mechanisms influencing peripheral motor axon degeneration remain largely unknown. A recent report showed a pathogenic role for c-Kit-expressing mast cells mediating inflammation and neuromuscular junction denervation in muscles from SOD1G93A rats. Here, we have explored whether mast cells infiltrate skeletal muscles in autopsied muscles from ALS patients. We report that degranulating mast cells were abundant in the quadriceps muscles from ALS subjects but not in controls. Mast cells were associated with myofibers and motor endplates and, remarkably, interacted with neutrophils forming large extracellular traps. Mast cells and neutrophils were also abundant around motor axons in the extensor digitorum longus muscle, sciatic nerve, and ventral roots of symptomatic SOD1G93A rats, indicating that immune cell infiltration extends along the entire peripheral motor pathway. Postparalysis treatment of SOD1G93A rats with the tyrosine kinase inhibitor drug masitinib prevented mast cell and neutrophil infiltration, axonal pathology, secondary demyelination, and the loss of type 2B myofibers, compared with vehicle-treated rats. These findings provide further evidence for a yet unrecognized contribution of immune cells in peripheral motor pathway degeneration that can be therapeutically targeted by tyrosine kinase inhibitors.
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ISSN:2379-3708
2379-3708
DOI:10.1172/jci.insight.123249