Modulation of Microglia by Voluntary Exercise or CSF1R Inhibition Prevents Age-Related Loss of Functional Motor Units

Cell Rep. 2019 Nov 5;29(6):1539-1554.e7. doi: 10.1016/j.celrep.2019.10.003.

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.

Keywords: CSF1R inhibition; aging; exercise; innervation; microglia; motor unit; neuroinflammation; neuromuscular junction; neuromuscular system; spinal cord.

MeSH terms

  • Aging / metabolism*
  • Aging / pathology
  • Animals
  • Cell Line
  • Databases, Genetic
  • Humans
  • Induced Pluripotent Stem Cells
  • Macrophages
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microglia / enzymology
  • Microglia / metabolism*
  • Microglia / physiology
  • Motor Neurons / cytology
  • Motor Neurons / metabolism*
  • Motor Neurons / pathology
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / physiopathology
  • Neuromuscular Junction / metabolism
  • Neuronal Plasticity / genetics
  • Physical Conditioning, Animal / physiology*
  • RNA-Seq
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor / antagonists & inhibitors*
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor / genetics
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor / metabolism
  • Spinal Cord / enzymology
  • Spinal Cord / metabolism
  • Spinal Cord / physiopathology

Substances

  • Csf1r protein, mouse
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor