Cell Type-Specific Alterations in Excitability and Inhibition of Upper Motor Neurons in AlsinKO Mice, a Model of Juvenile Onset ALS.

In amyotrophic lateral sclerosis (ALS) motor cortex, hyperexcitability is detected in both familial and sporadic cases, suggesting its centrality in the ALS phenotype; the underlying mechanisms, however, remain largely obscure. Here we utilize male and female UCHL1-eGFP (UeGFP) mice, in which the corticospinal neurons of the motor cortex are labeled with green fluorescent protein, to investigate the intrinsic excitability and synaptic inhibitory inputs on distinct neuron populations in WT-UeGFP and presymptomatic AlsinKO-UeGFP mice, which lack Alsin function and are a well-characterized mouse model for juvenile cases of ALS. We show that in the motor cortex of AlsinKO-UeGFP mice, eGFP-positive layer 5 pyramidal neurons, which represent upper motor neurons, show a decrease in intrinsic excitability compared with WT, whereas the electrophysiological properties of eGFP-negative cells, which identify callosal projection neurons, are unaffected. This alteration in intrinsic excitability, however, is counterbalanced by a decrease in the frequency of spontaneous inhibitory currents due to a cell-specific reduction in the number of inhibitory synaptic contacts on upper motor neurons. Thus, the overall excitability of upper motor neurons only displays negligible changes despite large alterations in intrinsic excitability and inhibitory synaptic input, which may explain why mice do not exhibit a prominent motor phenotype. The presence of this homeostatic interaction between intrinsic excitability and synaptic inhibition raises the question of which of the two changes is primary, and which is secondary, and shows that decreased function of motor cortex interneurons is an early event in ALS with Alsin mutations.