Phenotypic manifestation of α-synuclein strains derived from Parkinson's disease and multiple system atrophy in human dopaminergic neurons

alpha -Synuclein is critical in the pathogenesis of Parkinson's disease and related disorders, yet it remains unclear how its aggregation causes degeneration of human dopaminergic neurons. In this study, we induced alpha -synuclein aggregation in human iPSC-derived dopaminergic neurons using fibrils generated de novo or amplified in the presence of brain homogenates from Parkinson's disease or multiple system atrophy. Increased alpha -synuclein monomer levels promote seeded aggregation in a dose and time-dependent manner, which is associated with a further increase in alpha -synuclein gene expression. Progressive neuronal death is observed with brain-amplified fibrils and reversed by reduction of intraneuronal alpha -synuclein abundance. We identified 56 proteins differentially interacting with aggregates triggered by brain-amplified fibrils, including evasion of Parkinson's disease-associated deglycase DJ-1. Knockout of DJ-1 in iPSC-derived dopaminergic neurons enhance fibril-induced aggregation and neuronal death. Taken together, our results show that the toxicity of alpha -synuclein strains depends on aggregate burden, which is determined by monomer levels and conformation which dictates differential interactomes. Our study demonstrates how Parkinson's disease-associated genes influence the phenotypic manifestation of strains in human neurons. alpha -Synuclein aggregation contributes to Parkinson's disease and related disorders. Here the authors investigate patterns of alpha -synuclein aggregation in human dopaminergic neurons in response to fibrils derived from individuals with Parkinson's disease or multiple system atrophy.

Automated summary

Alpha-synuclein plays a critical role in the pathogenesis of Parkinson's disease and related disorders, causing degeneration of human dopaminergic neurons. The toxicity of alpha-synuclein strains depends on aggregate burden, determined by monomer levels and conformation, and influenced by differential interactomes. Parkinson's disease-associated genes influence the phenotypic manifestation of strains in human neurons.