Dynamic neuromuscular remodeling precedes motor-unit loss in a mouse model of ALS.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30320556.
- Also identified by DOI 10.7554/eLife.41973 and PMC identifier 6234026.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Despite being an early event in ALS, it remains unclear whether the denervation of neuromuscular junctions (NMJ) is simply the first manifestation of a globally degenerating motor neuron. Using in vivo imaging of single axons and their NMJs over a three-month period, we identify that single motor-units are dismantled asynchronously in <i>SOD1<sup>G37R</sup></i> mice. We reveal that weeks prior to complete axonal degeneration, the dismantling of axonal branches is accompanied by contemporaneous new axonal sprouting resulting in synapse formation onto nearby NMJs. Denervation events tend to propagate from the first lost NMJ, consistent with a contribution of neuromuscular factors extrinsic to motor neurons, with distal branches being more susceptible. These results show that NMJ denervation in ALS is a complex and dynamic process of continuous denervation and new innervation rather than a manifestation of sudden global motor neuron degeneration.
Medical subject headings
- Amyotrophic Lateral Sclerosis
- Motor Neurons
- Neuromuscular Junction
- Superoxide Dismutase