Tilorone mitigates the propagation of α-synucleinopathy in a midbrain-like organoid model

• Published in: Journal of translational medicine 2024-09, Vol.22 (1), p.816-14, Article 816
• Main Authors: Zhang, Qi, Liu, Meng, Xu, Yue, Lee, Juhyung, Jones, Brothely, Li, Bing, Huang, Wenwei, Ye, Yihong, Zheng, Wei
• Format: Article
• Language: English
• Subjects: alpha-Synuclein - metabolism; Animals; Apoptosis - drug effects; Drug preclinical development; Humans; Mesencephalon - drug effects; Mesencephalon - metabolism; Mesencephalon - pathology; Mice; Midbrain-like organoid; Models, Biological; Organoids - drug effects; Organoids - metabolism; Organoids - pathology; Parkinson Disease - drug therapy; Parkinson Disease - metabolism; Parkinson Disease - pathology; Parkinson’s disease; Phosphorylation - drug effects; Proteomics; Synucleinopathies - drug therapy; Synucleinopathies - metabolism; Synucleinopathies - pathology; Tilorone; α-synuclein
• ISSN: 1479-5876; 1479-5876
• DOI: 10.1186/s12967-024-05551-7

Parkinson's disease (PD) is a neurodegenerative condition characterized by the loss of dopaminergic neurons and the accumulation of Lewy-body protein aggregates containing misfolded α-synuclein (α-syn) in a phosphorylated form. The lack of effective models for drug screens has hindered drug development studies for PD. However, the recent development of in vitro brain-like organoids provides a new opportunity for evaluating therapeutic agents to slow the progression of this chronic disease. In this study, we used a 3D brain-like organoid model to investigate the potential of repurposing Tilorone, an anti-viral drug, for impeding the propagation of α-synucleinopathy. We assessed the effect of Tilorone on the uptake of fluorescently labeled α-syn preformed fibrils (sPFF) and sPFF-induced apoptosis using confocal microscopy. We also examined Tilorone's impact on the phosphorylation of endogenous α-syn induced by pathogenic sPFF by immunoblotting midbrain-like organoid extracts. Additionally, quantitative RT-PCR and proteomic profiling of sPFF-treated organoids were conducted to evaluate the global impact of Tilorone treatment on tissue homeostasis in the 3D organoid model. Tilorone inhibits the uptake of sPFF in both mouse primary neurons and human midbrain-like organoids. Tilorone also reduces the phosphorylation of endogenous α-syn induced by pathogenic α-syn fibrils and mitigates α-syn fibril-induced apoptosis in midbrain-like organoids. Proteomic profiling of fibril-treated organoids reveals substantial alterations in lipid homeostasis by α-syn fibrils, which are reversed by Tilorone treatment. Given its safety profile in clinics, Tilorone may be further developed as a therapeutic intervention to alleviate the propagation of synucleinopathy in PD patients.