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NLRP3 inflammasome activation in macrophage cell lines by prion protein fibrils as the source of IL-...

NLRP3 inflammasome activation in macrophage cell lines by prion protein fibrils as the source of IL-...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3508391

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

About this item

Full title

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

Publisher

Basel: Springer-Verlag

Journal title

Cellular and molecular life sciences : CMLS, 2012-12, Vol.69 (24), p.4215-4228

Language

English

Formats

Publication information

Publisher

Basel: Springer-Verlag

More information

Scope and Contents

Contents

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

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3508391

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3508391

Other Identifiers

ISSN

1420-682X

E-ISSN

1420-9071

DOI

10.1007/s00018-012-1140-0

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