Activation of Muscle-Specific Kinase (MuSK) Reduces Neuromuscular Defects in the Delta7 Mouse Model of Spinal Muscular Atrophy (SMA)

Int J Mol Sci. 2021 Jul 27;22(15):8015. doi: 10.3390/ijms22158015.

Abstract

Spinal muscular atrophy (SMA) is a motor neuron disease caused by insufficient levels of the survival motor neuron (SMN) protein. One of the most prominent pathological characteristics of SMA involves defects of the neuromuscular junction (NMJ), such as denervation and reduced clustering of acetylcholine receptors (AChRs). Recent studies suggest that upregulation of agrin, a crucial NMJ organizer promoting AChR clustering, can improve NMJ innervation and reduce muscle atrophy in the delta7 mouse model of SMA. To test whether the muscle-specific kinase (MuSK), part of the agrin receptor complex, also plays a beneficial role in SMA, we treated the delta7 SMA mice with an agonist antibody to MuSK. MuSK agonist antibody #13, which binds to the NMJ, significantly improved innervation and synaptic efficacy in denervation-vulnerable muscles. MuSK agonist antibody #13 also significantly increased the muscle cross-sectional area and myofiber numbers in these denervation-vulnerable muscles but not in denervation-resistant muscles. Although MuSK agonist antibody #13 did not affect the body weight, our study suggests that preservation of NMJ innervation by the activation of MuSK may serve as a complementary therapy to SMN-enhancing drugs to maximize the therapeutic effectiveness for all types of SMA patients.

Keywords: denervation; innervation; muscle-specific kinase (MuSK); neuromuscular junction; skeletal muscle; spinal muscular atrophy.

MeSH terms

  • Animals
  • Disease Models, Animal
  • Enzyme Activation
  • Mice
  • Mice, Transgenic
  • Motor Neurons / enzymology*
  • Motor Neurons / pathology
  • Muscular Atrophy, Spinal / enzymology*
  • Muscular Atrophy, Spinal / genetics
  • Muscular Atrophy, Spinal / pathology
  • Neuromuscular Junction / enzymology*
  • Neuromuscular Junction / genetics
  • Neuromuscular Junction / pathology
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptor Protein-Tyrosine Kinases / metabolism*
  • Survival of Motor Neuron 1 Protein / genetics
  • Survival of Motor Neuron 1 Protein / metabolism

Substances

  • Smn1 protein, mouse
  • Survival of Motor Neuron 1 Protein
  • MuSK protein, mouse
  • Receptor Protein-Tyrosine Kinases