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bioRxiv · 10.1101/2020.11.17.387449

Rab27 GTPases regulate alpha-synuclein uptake, cell-to-cell 1 transmission, and toxicity

Underwood, R. N.·Wang, B.·Pathak, A.·Volpicelli-Daley, L.·Yacoubian, T. A.
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Abstract

Parkinsons disease and Dementia with Lewy Bodies are two common neurodegenerative disorders marked by proteinaceous aggregates composed primarily of the protein -synuclein. -Synuclein is hypothesized to have prion-like properties, by which misfolded -synuclein induces the pathological aggregation of endogenous -synuclein and neuronal loss. Rab27a and Rab27b are two highly homologous Rab GTPases that regulate -synuclein secretion, clearance, and toxicity in vitro. In this study, we tested the impact of Rab27a/b on the transmission of pathogenic -synuclein. Double knockout of both Rab27 isoforms eliminated -synuclein aggregation and neuronal toxicity in primary cultured neurons exposed to fibrillary -synuclein. In vivo, Rab27 double knockout mice lacked fibril-induced -synuclein inclusions, dopaminergic neuron loss, and behavioral deficits seen in wildtype mice with fibril-induced inclusions. Studies using AlexaFluor488-labeled -synuclein fibrils revealed that Rab27a/b knockout prevented -synuclein internalization without affecting bulk endocytosis. Rab27a/b knockout also blocked the cell-to-cell spread of -synuclein pathology in multifluidic, multichambered devices. This study provides critical insight into the role of Rab GTPases in Parkinsons disease and identifies Rab27s as key players in the progression of synucleinopathies.

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Underwood, R. N., Wang, B., Pathak, A., Volpicelli-Daley, L., Yacoubian, T. A.. 2020-11-17. Rab27 GTPases regulate alpha-synuclein uptake, cell-to-cell 1 transmission, and toxicity. https://doi.org/10.1101/2020.11.17.387449

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