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Initiation and propagation of alpha synuclein oligomers--Relevance for Parkinson s disease

Subject Area Molecular and Cellular Neurology and Neuropathology
Term from 2016 to 2024
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 282604822
 
Final Report Year 2025

Final Report Abstract

Parkinson’s disease (PD) is a neurodegenerative disorder characterized by the accumulation of alpha-synuclein (α-syn) protein aggregates, leading to neuronal dysfunction and progressive motor impairment. The Emmy Noether Program aimed to investigate the mechanisms of α-syn propagation focusing on three key hypotheses. The first hypothesis explored how specific α-syn oligomers spread between neurons and other cell types, potentially driving neurodegeneration. Using advanced transgenic mouse models, we demonstrate the presence of α-syn oligomers in different brain regions and their transmission between neurons. Age-dependent accumulation of these oligomers correlated with motor deficits and dopaminergic neuron loss. The second hypothesis investigated the interaction between α-syn and immune cells, particularly monocytes and microglia. We found that α-syn oligomers, especially those associated with extracellular vesicles (EVs), strongly activated monocytes and induced inflammatory responses. These findings support the idea that immune dysregulation contributes to PD pathology, as PD patient-derived EVs triggered stronger immune reactions than those from healthy individuals. The third hypothesis examined the role of EV microRNAs in PD-related neurodegeneration. Although we identified several dysregulated miRNAs in PD serum, their diagnostic value was limited. Consequently, the study pivoted to analyzing mitochondrial DNA and blood cell transcriptomes in amyotrophic lateral sclerosis (ALS) patients, yielding valuable insights into neurodegenerative disease mechanisms. Overall, this research significantly advances our understanding of PD pathogenesis by elucidating α-syn transmission, immune activation, and molecular biomarkers.

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