Alpha-Synuclein: The Spark That Flames Dopaminergic Neurons, In Vitro and In Vivo Evidence

Mitochondria, alpha-syn fibrils and the endo-lysosomal system are key players in the pathophysiology of Parkinson's disease. The toxicity of alpha-syn is amplified by cell-to-cell transmission and aggregation of endogenous species in newly invaded neurons. Toxicity of alpha-syn PFF was investigated using primary cultures of dopaminergic neurons or on aged mice after infusion in the SNpc and combined with mild inhibition of GBA. In primary dopaminergic neurons, application of alpha-syn PFF induced a progressive cytotoxicity associated with mitochondrial dysfunction, oxidative stress, and accumulation of lysosomes suggesting that exogenous alpha-syn reached the lysosome (from the endosome). Counteracting the alpha-syn endocytosis with a clathrin inhibitor, dopaminergic neuron degeneration was prevented. In vivo, alpha-syn PFF induced progressive neurodegeneration of dopaminergic neurons associated with motor deficits. Histology revealed progressive aggregation of alpha-syn and microglial activation and accounted for the seeding role of alpha-syn, injection of which acted as a spark suggesting a triggering of cell-to-cell toxicity. We showed for the first time that a localized SNpc alpha-syn administration combined with a slight lysosomal deficiency and aging triggered a progressive lesion. The cellular and animal models described could help in the understanding of the human disease and might contribute to the development of new therapies.

Automated summary

Mitochondria, alpha-syn fibrils, and the endo-lysosomal system play important roles in the development of Parkinson's disease. The toxicity of alpha-syn is increased by cell-to-cell transmission and aggregation. This study used dopaminergic neuron cultures and aged mice as models and found that exogenous alpha-syn causes cytotoxicity by affecting mitochondrial function, oxidative stress, and lysosomal accumulation. Inhibiting the endocytosis of alpha-syn prevents neurodegeneration in dopaminergic neurons, while injection of alpha-syn in vivo leads to progressive neurodegeneration and motor deficits.