| Literature DB >> 25220759 |
Eve Peeraer1, Astrid Bottelbergs1, Kristof Van Kolen1, Ilie-Cosmin Stancu2, Bruno Vasconcelos2, Michel Mahieu1, Hilde Duytschaever1, Luc Ver Donck1, An Torremans3, Ellen Sluydts3, Nathalie Van Acker3, John A Kemp1, Marc Mercken1, Kurt R Brunden4, John Q Trojanowski4, Ilse Dewachter2, Virginia M Y Lee4, Diederik Moechars5.
Abstract
Neurofibrillary tangles composed of hyperphosphorylated fibrillized tau are found in numerous tauopathies including Alzheimer's disease. Increasing evidence suggests that tau pathology can be transmitted from cell-to-cell; however the mechanisms involved in the initiation of tau fibrillization and spreading of disease linked to progression of tau pathology are poorly understood. We show here that intracerebral injections of preformed synthetic tau fibrils into the hippocampus or frontal cortex of young tau transgenic mice expressing mutant human P301L tau induces tau hyperphosphorylation and aggregation around the site of injection, as well as a time-dependent propagation of tau pathology to interconnected brain areas distant from the injection site. Furthermore, we show that the tau pathology as a consequence of injection of tau preformed fibrils into the hippocampus induces selective loss of CA1 neurons. Together, our data confirm previous studies on the seeded induction and the spreading of tau pathology in a different tau transgenic mouse model and reveals neuronal loss associated with seeded tau pathology in tau transgenic mouse brain. These results further validate the utility of the tau seeding model in studying disease transmission, and provide a more complete in vivo tauopathy model with associated neurodegeneration which can be used to investigate the mechanisms involved in tau aggregation and spreading, as well as aid in the search for disease modifying treatments for Alzheimer's disease and related tauopathies.Entities:
Keywords: Cell death; Seeding; Spreading; Tau pathology
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Year: 2014 PMID: 25220759 PMCID: PMC4303592 DOI: 10.1016/j.nbd.2014.08.032
Source DB: PubMed Journal: Neurobiol Dis ISSN: 0969-9961 Impact factor: 5.996