Article
The ALS disease-associated mutant TDP-43 impairs mitochondrial dynamics and function in motor neurons.
Human molecular genetics - 1 Dec 2013
Wang Wenzhang, Li Li, Lin Wen-Lang, Dickson Dennis W, Petrucelli Leonard, Zhang Teng, Wang Xinglong
Abstract excerpt
Mutations in TDP-43 lead to familial ALS. Expanding evidence suggests that impaired mitochondrial dynamics likely contribute to the selective degeneration of motor neurons in SOD1-associated ALS. In this study, we investigated whether and how TDP-43 mutations might impact mitochondrial dynamics and function. We demonstrated that overexpression of wild-type TDP-43 resulted in reduced mitochondrial length and...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
