| Literature DB >> 30084913 |
Elisa R Zanier1, Ilaria Bertani1, Eliana Sammali1,2, Francesca Pischiutta1, Maria Antonietta Chiaravalloti1, Gloria Vegliante1, Antonio Masone1, Alessandro Corbelli3, Douglas H Smith4, David K Menon5, Nino Stocchetti6,7, Fabio Fiordaliso3, Maria-Grazia De Simoni1, William Stewart8,9, Roberto Chiesa1.
Abstract
Traumatic brain injury is a risk factor for subsequent neurodegenerative disease, including chronic traumatic encephalopathy, a tauopathy mostly associated with repetitive concussion and blast, but not well recognized as a consequence of severe traumatic brain injury. Here we show that a single severe brain trauma is associated with the emergence of widespread hyperphosphorylated tau pathology in a proportion of humans surviving late after injury. In parallel experimental studies, in a model of severe traumatic brain injury in wild-type mice, we found progressive and widespread tau pathology, replicating the findings in humans. Brain homogenates from these mice, when inoculated into the hippocampus and overlying cerebral cortex of naïve mice, induced widespread tau pathology, synaptic loss, and persistent memory deficits. These data provide evidence that experimental brain trauma induces a self-propagating tau pathology, which can be transmitted between mice, and call for future studies aimed at investigating the potential transmissibility of trauma associated tau pathology in humans.Entities:
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Year: 2018 PMID: 30084913 PMCID: PMC6113646 DOI: 10.1093/brain/awy193
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501