Dynamic neuromuscular remodeling precedes motor-unit loss in a mouse model of ALS

Author:

Martineau Éric12ORCID,Di Polo Adriana13ORCID,Vande Velde Christine13,Robitaille Richard12ORCID

Affiliation:

1. Département de neurosciences, Université de Montréal, Québec, Canada

2. Groupe de recherche sur le système nerveux central, Université de Montréal, Québec, Canada

3. Centre de recherche du Centre Hospitalier de l'Université de Montréal, Québec, Canada

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 SOD1G37R 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.

Funder

Canadian Institutes of Health Research

Canadian Foundation for Innovation

ALS Society of Canada

Muscular Dystrophy Association

Fonds de Recherche du Québec - Santé

Robert Packard Center for ALS Research, Johns Hopkins University

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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