Journal of Clinical Investigation · 2006 · 147 citations · 36 references
Life SciencesMolecular BiologyNeuroscienceMolecular NeurobiologyMolecular NeurosciencePrion DiseasesAnimal Prion DiseasesMolecular Basis Of NeurodegenerationNeurodegenerative DiseasesNeurodegenerative DisordersPrion Protein MisfoldingRna InterferenceMouse Embryonic Stem CellsPrion Disease ModelsProtease ResistanceProtease-resistant Prion ProteinRna Interference ConstructsRna Interference-mediated SuppressionShort Hairpin RnaTransgenic Mice
Prion diseases are fatal neurodegenerative diseases characterized by the accumulation of PrP(Sc), the infectious and protease-resistant form of the cellular prion protein (PrP(C)). We generated lentivectors expressing PrP(C)-specific short hairpin RNAs (shRNAs) that efficiently silenced expression of the prion protein gene (Prnp) in primary neuronal cells. Treatment of scrapie-infected neuronal cells with these lentivectors resulted in an efficient and stable suppression of PrP(Sc) accumulation. After intracranial injection, lentiviral shRNA reduced PrP(C) expression in transgenic mice carrying multiple copies of Prnp. To test the therapeutic potential of lentiviral shRNA, we used what we believe to be a novel approach in which the clinical situation was mimicked. We generated chimeric mice derived from lentivector-transduced embryonic stem cells. Depending on the degree of chimerism, these animals carried the lentiviral shRNAs in a certain percentage of brain cells and expressed reduced levels of PrP(C). Importantly, in highly chimeric mice, survival after scrapie infection was significantly extended. Taken together, these data suggest that lentivector-mediated RNA interference could be an approach for the treatment of prion disease.
36
Novel Proteinaceous Infectious Particles Cause Scrapie
Stanley B. Prusiner · Science · 1982 · 5.1K citations
Veterinary Medicine, Infectious Diseases, Molecular Biology +10
Mice devoid of PrP are resistant to scrapie
Hansruedi Büeler, Adriano Aguzzi, Andreas W. Sailer et al. · Cell · 1993 · 2.1K citations · Full text