PrP-deficient mice are resistant to scrapie.

Détails

ID Serval
serval:BIB_C8A41C1328DC
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
PrP-deficient mice are resistant to scrapie.
Périodique
Annals of the New York Academy of Sciences
Auteur⸱e⸱s
Weissmann C., Büeler H., Fischer M., Sailer A., Aguzzi A., Aguet M.
ISSN
0077-8923 (Print)
ISSN-L
0077-8923
Statut éditorial
Publié
Date de publication
1994
Volume
724
Pages
235-240
Langue
anglais
Résumé
Prusiner proposed that the infectious agent of scrapie, the prion, is PrPSc, a modified form of the normal host protein PrPC. Prn-p0/0 mice devoid of PrPC showed normal development and behavior. When inoculated with mouse scrapie prions they remained free of scrapie symptoms for at least 16 months while wild type controls all died within 6 months. Propagation of infectivity in the PrP null mice, if any, was less than 10(-5) that in wild type animals. Surprisingly, heterozygous Prn-p0/+ mice also showed enhanced resistance to scrapie. After introduction of Syrian hamster PrP transgenes, Prn-p0/0 mice became highly susceptible to hamster but not to mouse prions. These experiments show that PrPC, possibly at close to normal levels, is required for the usual susceptibility to scrapie and that lack of homology between incoming prions and the host's PrP genes retards disease.
Mots-clé
Animals, Brain/metabolism, Brain/microbiology, Cricetinae, Genetic Complementation Test, Immunity, Innate, Mesocricetus, Mice, Mice, Mutant Strains, Prions/genetics, Scrapie/genetics, Scrapie/immunology, Spleen/metabolism, Spleen/microbiology
Pubmed
Web of science
Création de la notice
28/01/2008 11:36
Dernière modification de la notice
20/08/2019 15:43
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