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NLRP3 inflammasome activation in macrophage cell lines by prion protein fibrils as the source of IL-1β and neuronal toxicity

Prion diseases are fatal transmissible neurodegenerative diseases, characterized by aggregation of the pathological form of prion protein, spongiform degeneration, neuronal loss and activation of astrocytes and microglia. Microglia can clear prion plaques but on the other hand cause neuronal death v...

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Main Authors: Hafner-Bratkovič, Iva, Benčina, Mojca, Fitzgerald, Katherine A., Golenbock, Douglas, Jerala, Roman
Formato: Artigo
Idioma:Inglês
Publicado: 2012
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3508391/
https://ncbi.nlm.nih.gov/pubmed/22926439
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00018-012-1140-0
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