A seeding-based neuronal model of tau aggregation for use in drug discovery

• Published in: PloS one Vol. 18; no. 4; p. e0283941
• Main Authors: Amorim, Ines S, Challal, Sylvie, Cistarelli, Laetitia, Dorval, Thierry, Abjean, Laurene, Touzard, Manuelle, Arbez, Nicolas, François, Arnaud, Panayi, Fany, Jeggo, Ross, Cecon, Erika, Oishi, Atsuro, Dam, Julie, Jockers, Ralf, Machado, Patricia
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 04.04.2023; Public Library of Science (PLoS)
• Subjects: Accumulation; Alzheimer Disease - pathology; Alzheimer's disease; Alzheimers disease; Animals; Biology and Life Sciences; Biosensors; Brain - metabolism; Cells; Data analysis; Drug Discovery; Engineering and Technology; Evaluation; Health aspects; Human health and pathology; Humans; Inclusions; Intracellular; Laboratories; Life Sciences; Medicine and Health Sciences; Mice; Mice, Transgenic; Modelling; Mutation; Neurobiology; Neurodegenerative diseases; Neurons; Neurons - metabolism; Neurons and Cognition; Paralysis; Pathology; Patients; Progressive supranuclear palsy; Protein seeding; Proteins; Research and Analysis Methods; Robust control; Seeding; Seeds; siRNA; Tau protein; Tau proteins; tau Proteins - genetics; tau Proteins - metabolism; Tauopathies - metabolism; Transgenic animals; France
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0283941

Intracellular accumulation of tau protein is a hallmark of Alzheimer's Disease and Progressive Supranuclear Palsy, as well as other neurodegenerative disorders collectively known as tauopathies. Despite our increasing understanding of the mechanisms leading to the initiation and progression of tau pathology, the field still lacks appropriate disease models to facilitate drug discovery. Here, we established a novel and modulatable seeding-based neuronal model of full-length 4R tau accumulation using humanized mouse cortical neurons and seeds from P301S human tau transgenic animals. The model shows specific and consistent formation of intraneuronal insoluble full-length 4R tau inclusions, which are positive for known markers of tau pathology (AT8, PHF-1, MC-1), and creates seeding competent tau. The formation of new inclusions can be prevented by treatment with tau siRNA, providing a robust internal control for use in qualifying the assessment of potential therapeutic candidates aimed at reducing the intracellular pool of tau. In addition, the experimental set up and data analysis techniques used provide consistent results in larger-scale designs that required multiple rounds of independent experiments, making this is a versatile and valuable cellular model for fundamental and early pre-clinical research of tau-targeted therapies.