Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie

Alex J Raeber, Richard E Race, Sebastian Brandner, Suzette A. Priola, Andreas Sailer, Richard A Bessen, Lennart Mucke, Jean Manson, Adriano Aguzzi, Michael B A Oldstone, Charles Weissmann, Bruce Chesebro

Research output: Contribution to journalArticlepeer-review


Transmissible spongiform encephalopathies are characterized by spongiosis, astrocytosis and accumulation of PrPSc, an isoform of the normal host protein PrPC. The exact cell types responsible for agent propagation and pathogenesis are still uncertain. To determine the possible role of astrocytes, we generated mice devoid of murine PrP but expressing hamster PrP transgenes driven by the astrocyte-specific GFAP promoter. After inoculation with hamster scrapie, these mice accumulated infectivity and PrPSc to high levels, developed severe disease after 227 +/- 5 days and died 7 +/- 4 days later. Therefore, astrocytes could play an important role in scrapie pathogenesis, possibly by an indirect toxic effect on neurons. Interestingly, mice expressing the same transgenes but also endogenous murine PrP genes propagated infectivity without developing disease.
Original languageEnglish
Pages (from-to)6057-65
Number of pages9
JournalEMBO Journal
Issue number20
Publication statusPublished - 15 Oct 1997


  • Animals
  • Astrocytes/metabolism
  • Biological Assay
  • Brain/pathology
  • Cricetinae
  • Disease Susceptibility
  • Glial Fibrillary Acidic Protein/genetics
  • Mice
  • Mice, Knockout
  • PrPSc Proteins/biosynthesis
  • PrPSc Proteins/genetics
  • Prions/biosynthesis
  • Prions/genetics
  • RNA, Messenger/analysis
  • Recombinant Fusion Proteins/biosynthesis
  • Rodent Diseases/etiology
  • Rodent Diseases/mortality
  • Scrapie/etiology
  • Scrapie/mortality


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