Reduced TDP-43 Expression Improves Neuronal Activities in a Drosophila Model of Perry Syndrome.

ABSTRACT: Parkinsonian Perry syndrome, involving mutations in the dynein motor component dynactin or p150^Glued, is characterized by TDP-43 pathology in affected brain regions, including the substantia nigra. However, the molecular relationship between p150^Glued and TDP-43 is largely unknown. Here, we report that a reduction in TDP-43 protein levels alleviates the synaptic defects of neurons expressing the Perry mutant p150^G50R in Drosophila. Dopaminergic expression of p150^G50R, which decreases dopamine release, disrupts motor ability and reduces the lifespan of Drosophila. p150^G50R expression also causes aggregation of dense core vesicles (DCVs), which contain monoamines and neuropeptides, and disrupts the axonal flow of DCVs, thus decreasing sy

SUBMITTER: Hosaka Y 

PROVIDER: S-EPMC5514405 | biostudies-literature | 2017 Jul

REPOSITORIES: biostudies-literature