Locomotor deficits in a mouse model of ALS are paralleled by loss of V1-interneuron connections onto fast motor neurons

Ilary Allodi (), Roser Montañana-Rosell, Raghavendra Selvan, Peter Löw and Ole Kiehn ()
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Ilary Allodi: University of Copenhagen
Roser Montañana-Rosell: University of Copenhagen
Raghavendra Selvan: University of Copenhagen
Peter Löw: Karolinska Institutet
Ole Kiehn: University of Copenhagen

Nature Communications, 2021, vol. 12, issue 1, 1-18

Abstract: Abstract ALS is characterized by progressive inability to execute movements. Motor neurons innervating fast-twitch muscle-fibers preferentially degenerate. The reason for this differential vulnerability and its consequences on motor output is not known. Here, we uncover that fast motor neurons receive stronger inhibitory synaptic inputs than slow motor neurons, and disease progression in the SOD1G93A mouse model leads to specific loss of inhibitory synapses onto fast motor neurons. Inhibitory V1 interneurons show similar innervation pattern and loss of synapses. Moreover, from postnatal day 63, there is a loss of V1 interneurons in the SOD1G93A mouse. The V1 interneuron degeneration appears before motor neuron death and is paralleled by the development of a specific locomotor deficit affecting speed and limb coordination. This distinct ALS-induced locomotor deficit is phenocopied in wild-type mice but not in SOD1G93A mice after appearing of the locomotor phenotype when V1 spinal interneurons are silenced. Our study identifies a potential source of non-autonomous motor neuronal vulnerability in ALS and links ALS-induced changes in locomotor phenotype to inhibitory V1-interneurons.

Date: 2021
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DOI: 10.1038/s41467-021-23224-7

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