EphrinB2 knockdown in cervical spinal cord preserves diaphragm innervation in a mutant SOD1 mouse model of ALS.
Publication/Presentation Date
1-15-2024
Abstract
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by motor neuron loss. Importantly, non-neuronal cell types such as astrocytes also play significant roles in disease pathogenesis. However, mechanisms of astrocyte contribution to ALS remain incompletely understood. Astrocyte involvement suggests that transcellular signaling may play a role in disease. We examined contribution of transmembrane signaling molecule ephrinB2 to ALS pathogenesis, in particular its role in driving motor neuron damage by spinal cord astrocytes. In symptomatic SOD1
Volume
12
ISSN
2050-084X
Published In/Presented At
Urban, M. W., Charsar, B. A., Heinsinger, N. M., Markandaiah, S. S., Sprimont, L., Zhou, W., Brown, E. V., Henderson, N. T., Thomas, S. J., Ghosh, B., Cain, R. E., Trotti, D., Pasinelli, P., Wright, M. C., Dalva, M. B., & Lepore, A. C. (2024). EphrinB2 knockdown in cervical spinal cord preserves diaphragm innervation in a mutant SOD1 mouse model of ALS. eLife, 12, RP89298. https://doi.org/10.7554/eLife.89298
Disciplines
Business Administration, Management, and Operations | Health and Medical Administration | Management Sciences and Quantitative Methods
PubMedID
38224498
Department(s)
Administration and Leadership
Document Type
Article