Impairment of the glial phagolysosomal system drives prion-like propagation in a Drosophila model of Huntington's disease
Graham H. Davis, Aprem Zaya, Margaret M.P. Pearce
This study shows that mutant huntingtin aggregates impair glial phagocytosis and phagolysosomal function in Drosophila, leading to prion-like propagation of aggregates and neurodegeneration.
Journal of Neuroscience · Apr 8, 2024Peer-reviewedNeuroscience