| Literature DB >> 31693894 |
Elisa Giorgetti1, Moh Panesar2, Yunyu Zhang3, Stefanie Joller4, Marie Ronco2, Michael Obrecht2, Christian Lambert2, Nathalie Accart2, Nicolau Beckmann2, Arno Doelemeyer2, Ludovic Perrot5, Isabelle Fruh6, Matthias Mueller6, Eliane Pierrel2, Serge Summermatter2, Michael Bidinosti2, Derya R Shimshek4, Sophie Brachat2, Mark Nash7.
Abstract
Age-related loss of skeletal muscle innervation by motor neurons leads to impaired neuromuscular function and is a well-established clinical phenomenon. However, the underlying pathogenesis remains unclear. Studying mice, we find that the number of motor units (MUs) can be maintained by counteracting neurotoxic microglia in the aged spinal cord. We observe that marked innervation changes, detected by motor unit number estimation (MUNE), occur prior to loss of muscle function in aged mice. This coincides with gene expression changes indicative of neuronal remodeling and microglial activation in aged spinal cord. Voluntary exercise prevents loss of MUs and reverses microglia activation. Depleting microglia by CSF1R inhibition also prevents the age-related decline in MUNE and neuromuscular junction disruption, implying a causal link. Our results suggest that age-related changes in spinal cord microglia contribute to neuromuscular decline in aged mice and demonstrate that removal of aged neurotoxic microglia can prevent or reverse MU loss.Entities:
Keywords: CSF1R inhibition; aging; exercise; innervation; microglia; motor unit; neuroinflammation; neuromuscular junction; neuromuscular system; spinal cord
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Year: 2019 PMID: 31693894 DOI: 10.1016/j.celrep.2019.10.003
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423