| First Author | Martineau É | Year | 2020 |
| Journal | eNeuro | Volume | 7 |
| Issue | 1 | PubMed ID | 32033983 |
| Mgi Jnum | J:288533 | Mgi Id | MGI:6432129 |
| Doi | 10.1523/ENEURO.0388-19.2020 | Citation | Martineau E, et al. (2020) Sex-Specific Differences in Motor-Unit Remodeling in a Mouse Model of ALS. eNeuro 7(1):ENEURO.0388-19.2020 |
| abstractText | Progressive loss of neuromuscular junctions (NMJs) is an early event in amyotrophic lateral sclerosis (ALS), preceding the global degeneration of motor axons and being accompanied by new axonal sprouting within the same axonal arbor. Some aspects of ALS onset and progression seem to be affected by sex in animal models of the disease. However, whether there are sex-specific differences in the pattern or time course of NMJ loss and repair within single motor axons remains unknown. We performed further analysis of a previously published in vivo dataset, obtained from male and female SOD1(G37R) mice. We found that NMJ losses are as frequent in male and female motor axons but, intriguingly, axonal sprouting is more frequent in female than male mice, resulting in a net increase of axonal arborization. Interestingly, these numerous new axonal branches in female mice are associated with a slightly faster decline in grip strength, increased NMJ denervation, and reduced alpha-motor neuron survival. Collectively, these results suggest that excessive axonal sprouting and motor-unit (MU) expansion in female SOD1(G37R) mice are maladaptive during ALS progression. |
