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Publication : Bassoon contributes to tau-seed propagation and neurotoxicity.

First Author  Martinez P Year  2022
Journal  Nat Neurosci Volume  25
Issue  12 Pages  1597-1607
PubMed ID  36344699 Mgi Jnum  J:355376
Mgi Id  MGI:7486697 Doi  10.1038/s41593-022-01191-6
Citation  Martinez P, et al. (2022) Bassoon contributes to tau-seed propagation and neurotoxicity. Nat Neurosci 25(12):1597-1607
abstractText  Tau aggregation is a defining histopathological feature of Alzheimer's disease and other tauopathies. However, the cellular mechanisms involved in tau propagation remain unclear. Here, we performed an unbiased quantitative proteomic study to identify proteins that specifically interact with this tau seed. We identified Bassoon (BSN), a presynaptic scaffolding protein, as an interactor of the tau seed isolated from a mouse model of tauopathy, and from Alzheimer's disease and progressive supranuclear palsy postmortem samples. We show that BSN exacerbates tau seeding and toxicity in both mouse and Drosophila models for tauopathy, and that BSN downregulation decreases tau spreading and overall disease pathology, rescuing synaptic and behavioral impairments and reducing brain atrophy. Our findings improve the understanding of how tau seeds can be stabilized by interactors such as BSN. Inhibiting tau-seed interactions is a potential new therapeutic approach for neurodegenerative tauopathies.
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