KMID : 0892920230320030147
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Experimental Neurobiology 2023 Volume.32 No. 3 p.147 ~ p.156
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Monitoring ¥á-synuclein Aggregation Induced by Preformed ¥á-synuclein Fibrils in an In Vitro Model System
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Kim Beom-Jin
Noh Hye-Rin Jeon Hyong-Jun Park Sang-Myun
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Abstract
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Parkinson¡¯s disease (PD) is characterized by the presence of ¥á-synuclein (¥á-syn) inclusions in the brain and the degeneration of dopamine-producing neurons. There is evidence to suggest that the progression of PD may be due to the prion-like spread of ¥á-syn aggregates, so understanding and limiting ¥á-syn propagation is a key area of research for developing PD treatments. Several cellular and animal model systems have been established to monitor ¥á-syn aggregation and propagation. In this study, we developed an in vitro model using A53T ¥á-syn-EGFP overexpressing SH-SY5Y cells and validated its usefulness for high-throughput screening of potential therapeutic targets. Treatment with preformed recombinant ¥á-syn fibrils induced the formation of aggregation puncta of A53T ¥á-syn-EGFP in these cells, which were analyzed using four indices: number of dots per cell, size of dots, intensity of dots, and percentage of cells containing aggregation puncta. Four indices are reliable indicators of the effectiveness of interventions against ¥á-syn propagation in a one-day treatment model to minimize the screening time. This simple and efficient in vitro model system can be used for high-throughput screening to discover new targets for inhibiting ¥á-syn propagation.
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KEYWORD
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Parkinson disease, ¥á-synuclein, Protein aggregation, In vitro techniques
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