Recovery of altered neuromuscular junction morphology and muscle function in mdx mice after injury

• Published in: Cellular and molecular life sciences : CMLS 2015-01, Vol.72 (1), p.153-164
• Main Authors: Pratt, Stephen J. P, Shah, Sameer B, Ward, Christopher W, Kerr, Jaclyn P, Stains, Joseph P, Lovering, Richard M
• Format: Article
• Language: English
• Subjects: animal models; Animals; Biochemistry; Biomedical and Life Sciences; Biomedicine; Blotting, Western; Cell Biology; Cells, Cultured; Dystrophin - physiology; Dystrophy; Fluorescent Antibody Technique; Immunoprecipitation; Injuries; Life Sciences; Male; Mice; Mice, Inbred C57BL; Mice, Inbred mdx; microtubules; morphology; Muscle Contraction; muscle fibers; Muscles; Muscular dystrophy; Muscular Dystrophy, Duchenne - genetics; Muscular Dystrophy, Duchenne - metabolism; Muscular Dystrophy, Duchenne - pathology; neuromuscular disorders; Neuromuscular Junction - injuries; Neuromuscular Junction - metabolism; Neuromuscular Junction - physiopathology; Real-Time Polymerase Chain Reaction; Receptors, Cholinergic - metabolism; Regeneration - physiology; Research Article; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; Rodents; torque
• ISSN: 1420-682X; 1420-9071
• DOI: 10.1007/s00018-014-1663-7

Duchenne muscular dystrophy (DMD) is a devastating neuromuscular disease in which weakness, increased susceptibility to muscle injury, and inadequate repair underlie the pathology. While most attention has focused within the muscle fiber, we recently demonstrated significant alterations in the neuromuscular junction (NMJ) morphology and resulting neuromuscular transmission failure (NTF) 24 h after injury in mdx mice (murine model for DMD). Here we determine the contribution of NMJ morphology and NTF to the recovery of muscle contractile function post-injury. NMJ morphology and NTF rates were assessed day 0 (immediately after injury) and days 1, 7, 14 and 21 after quadriceps injury. Eccentric injury of the quadriceps resulted in a significant loss of maximal torque in both WT (39 ± 6 %) and mdx (76 ± 8 %) with a full recovery in WT by day 7 and in mdx by day 21. Post-injury alterations in NMJ morphology and NTF were found only in mdx, were limited to days 0 and 1, and were independent of changes in MuSK or AChR expression. Such early changes at the NMJ after injury are consistent with mechanical disruption rather than newly forming NMJs. Furthermore, we show that the dense microtubule network that underlies the NMJ is significantly reduced and disorganized in mdx compared to WT. These structural changes at the NMJ may play a role in the increased NMJ disruption and the exaggerated loss of nerve-evoked muscle force seen after injury to dystrophic muscles.