Article
Reduced TDP-43 Expression Improves Neuronal Activities in a Drosophila Model of Perry Syndrome.
EBioMedicine - 1 Jul 2017
Hosaka Yuka, Inoshita Tsuyoshi, Shiba-Fukushima Kahori, Cui Changxu, Arano Taku, Imai Yuzuru, Hattori Nobutaka
Abstract excerpt
Parkinsonian Perry syndrome, involving mutations in the dynein motor component dynactin or p150Glued, is characterized by TDP-43 pathology in affected brain regions, including the substantia nigra. However, the molecular relationship between p150Glued 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...
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