Journal of General Virology · 1995 · 184 citations · 13 references
Veterinary MedicineInfectious DiseasesNeurobiologyMolecular NeurobiologyNeuropathologyPrion DiseasesAnimal Prion DiseasesNervous TissuePrion Protein MisfoldingPrion Tissue TropismTissue Residue Distribution
A cellular form of the prion protein (PrPC) is thought to be a substrate for an abnormal isoform of th eprion protein (PrPSc) in scrapie. PrPC is abundant in tissues of the central nervous system, but little is known about the distribution of PrPC in non-neuronal tissues of sheep, the natural host of scrapie. This study investigated the tissue distribution of PrPC in sheep. Although PrPC was abundant in neuronal tissues, it was detected in non-neuronal tissues such as spleen, lymph node, lung, heart, kidney, skeletal muscle, uterus, adrenal gland, parotid gland, intestine, proventriculus, abomasum and mammary gland. Neither PrPC nor PrP mRNA was detected in the liver. The tissue distribution of PrPC appears to be inconsistent with the tissues which possess scrapie infectivity, suggesting that factor(s) specific to certain cell types may be required to support multiplication of the scrapie agent.
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Mice devoid of PrP are resistant to scrapie
Hansruedi Büeler, Adriano Aguzzi, Andreas W. Sailer et al. · Cell · 1993 · 2.1K citations · Full text
Prion protein is necessary for normal synaptic function
John Collinge, Miles A. Whittington, Katie Sidle et al. · Nature · 1994 · 792 citations
Bovine spongiform encephalopathy: epidemiological studies.
J. W. Wilesmith, G. Wells, M. P. Cranwell et al. · PubMed · 1988 · 715 citations
Veterinary Medicine, Animal Sciences, Veterinary Epidemiology +12