Characterization of neuromuscular synapse function abnormalities in multiple Duchenne muscular dystrophy mouse models

• Published in: The European journal of neuroscience Vol. 43; no. 12; pp. 1623 - 1635
• Main Authors: van der Pijl, Elizabeth M., van Putten, Maaike, Niks, Erik H., Verschuuren, Jan J. G. M., Aartsma-Rus, Annemieke, Plomp, Jaap J.
• Format: Journal Article
• Language: English
• Published: France Blackwell Publishing Ltd 01.06.2016
• Subjects: acetylcholine receptor; Action Potentials; Animals; Disease Models, Animal; Dystrophin - genetics; electrophysiology; endplate; Female; Male; Mice; Mice, Inbred mdx; Mice, Knockout; Miniature Postsynaptic Potentials; Muscle Fatigue; Muscle Strength; Muscular Dystrophy, Duchenne - genetics; Muscular Dystrophy, Duchenne - metabolism; Muscular Dystrophy, Duchenne - physiopathology; neuromuscular junction; Neuromuscular Junction - metabolism; Neuromuscular Junction - physiopathology; Receptors, Cholinergic - metabolism; Respiration; Synaptic Transmission; Utrophin - genetics; acetylcholine receptor; synaptic transmission; electrophysiology; neuromuscular junction; endplate
• ISSN: 0953-816X; 1460-9568
• DOI: 10.1111/ejn.13249

Duchenne muscular dystrophy (DMD) is an X‐linked myopathy caused by dystrophin deficiency. Dystrophin is present intracellularly at the sarcolemma, connecting actin to the dystrophin‐associated glycoprotein complex. Interestingly, it is enriched postsynaptically at the neuromuscular junction (NMJ), but its synaptic function is largely unknown. Utrophin, a dystrophin homologue, is also concentrated at the NMJ, and upregulated in DMD. It is possible that the absence of dystrophin at NMJs in DMD causes neuromuscular transmission defects that aggravate muscle weakness. We studied NMJ function in mdx mice (lacking dystrophin) and wild type mice. In addition, mdx/utrn+/− and mdx/utrn−/− mice (lacking utrophin) were used to investigate influences of utrophin levels. The three Duchenne mouse models showed muscle weakness when comparatively tested in vivo, with mdx/utrn−/− mice being weakest. Ex vivo muscle contraction and electrophysiological studies showed a reduced safety factor of neuromuscular transmission in all models. NMJs had ~ 40% smaller miniature endplate potential amplitudes compared with wild type, indicating postsynaptic sensitivity loss for the neurotransmitter acetylcholine. However, nerve stimulation‐evoked endplate potential amplitudes were unchanged. Consequently, quantal content (i.e. the number of acetylcholine quanta released per nerve impulse) was considerably increased. Such a homeostatic compensatory increase in neurotransmitter release is also found at NMJs in myasthenia gravis, where autoantibodies reduce acetylcholine receptors. However, high‐rate nerve stimulation induced exaggerated endplate potential rundown. Study of NMJ morphology showed that fragmentation of acetylcholine receptor clusters occurred in all models, being most severe in mdx/utrn−/− mice. Overall, we showed mild ‘myasthenia‐like’ neuromuscular synaptic dysfunction in several Duchenne mouse models, which possibly affects muscle weakness and degeneration. Neuromuscular synaptic transmission deficits in Duchenne muscular dystrophy model mice. Decrement of compound muscle action potentials in repetitive nerve stimulation electromyography and increased sensitivity of muscle contraction for the acetylcholine receptor antagonist d‐tubocurarine. Micro‐electrode recordings revealed reductions of postsynaptic neurotransmitter sensitivity as well as extra rundown of endplate potentials during high‐rate activity. While muscle fibre degeneration is the main cause of weakness in DMD patients and model mice, neuromuscular synapse deficits may have additional negative influences.