NR AJLG
AU Piccardo,P.; Safar,J.G.; Ceroni,M.; Gajdusek,D.C.; Gibbs,C.J.Jr.
TI Immunohistochemical localization of prion protein in spongiform encephalopathies and normal brain tissue
QU Neurology 1990 Mar; 40(3 Pt 1): 518-22
PT journal article
AB We used polyclonal antibodies raised against hamster and mouse PrP27-30 as immunologic probes to study the localization of intracellular and extracellular deposits of prion protein in normal and scrapie-infected mouse and hamster brains and in Creutzfeldt-Jakob disease (CJD)-infected mouse brains. In addition, we examined normal human brain and brain tissues from patients with CJD, kuru, Alzheimer's disease, and idiopathic chronic encephalitis. There was positive staining in the cytoplasm of neurons of normal and scrapie- and CJD-infected mice, and in the neurons of normal and scrapie-infected hamsters. The staining pattern suggests the localization of PrP in an intracellular membrane compartment, most likely the rough endoplasmic reticulum or Golgi apparatus. Antibodies raised against a 15-amino-acid synthetic peptide of the N-terminal of hamster PrP27-30 displayed a similar pattern of staining in mouse brain sections. We observed no intracellular staining in human brain sections obtained at autopsy. Antibodies prepared against mouse and hamster PrP27-30 reacted with amyloid plaques in scrapie-infected mouse and kuru- and CJD-infected human brain sections but not with amyloid plaques in the brain of a patient with Alzheimer's disease.
MH Alzheimer Disease/metabolism; Amyloid/analysis; Animal; *Brain Chemistry; Creutzfeldt-Jakob Syndrome/*metabolism; Hamsters; Human; Immunohistochemistry; Kuru/*metabolism; Mice; PrP 27-30 Protein; Prions/*analysis; Scrapie/*metabolism; Staining and Labeling; Viral Proteins/*analysis
AD Laboratory of Central Nervous System Studies, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892.
SP englisch
PO USA