Annals of Neurology · 1995 · 33 citations · 23 references
Veterinary MedicineNeurologyNeuroscienceNeurodegenerationNeuropathologyPrion DiseasesCreutzfeldt-jakob DiseaseGerstmann-sträussler-scheinker DiseaseNervous System PathologyNeurodegenerative DiseasesNeurodegenerative DisordersNeuropathology Of Prion DiseaseAmyloid PlaquesCreutzfeldt-jakob Disease PathologyFatal Familial Insomnia NeuropathologyGerstmann SyndromeGerstmann-sträussler-scheinker Disease NeuropathologyIatrogenic Creutzfeldt-jakob DiseaseInfectious NeuropathologyNeuropathology Of Spongiform Change
We studied the regional distribution of infectious amyloid protein by western immunoblots of brain tissue extracts from 37 patients with different forms of spongiform encephalopathy, i.e., 16 sporadic cases, 18 familial cases with a variety of mutations, and 3 iatrogenic cases. In sporadic and familial Creutzfeldt-Jakob disease, amyloid protein concentrations were usually highest in the frontotemporal regions of the cerebral cortex, whereas iatrogenic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker syndrome had as high or higher concentrations in the deep cerebral nuclei and cerebellum. As a group, familial cases had lower amyloid protein concentrations than either sporadic or iatrogenic cases, and fatal familial insomnia patients had the lowest concentrations found in any form of disease. This hierarchy of amyloid protein concentrations corresponds to the experimental transmission rates observed for each form of disease and is consistent with the concept that the protein molecule is an integral component of the infectious agent. Regional amyloid protein pattern analysis of brain and spinal cord may help to distinguish sporadic from environmentally acquired infections, as for example, cases of human disease suspected to have arisen from exposure to sheep or cows infected with scrapie or bovine spongiform encephalopathy.
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Nearly ubiquitous tissue distribution of the scrapie agent precursor protein
Paul E. Bendheim, H. R. Brown, R. D. Rudelli et al. · Neurology · 1992 · 468 citations
Medicine, Neurobiology, Neuroscience +15
Lev G. Goldfarb, Paul Brown, W. Richard McCombie et al. · Proceedings of the National Academy of Sciences · 1991 · 332 citations · Full text
Life Sciences, Genetics, Neurology +17