| Literature DB >> 29105545 |
Beata Sikorska1, Agata Gajos2, Andrzej Bogucki2, Emil Zielonka1, Christina Sigurdson3, Pawel P Liberski1.
Abstract
We report here on the ultrastructure of amyloid plaques in chronic wasting disease (CWD) transmitted to Tg20 transgenic mice overexpressing prion protein (PrPc). We identified three main types of amyloid deposits in mCWD: large amyloid deposits, unicentric plaques similar to kuru plaques in human prion diseases and multicentric plaques reminiscent of plaques typical of GSS. The most unique type of plaques were large subpial amyloid deposits. They were composed of large areas of amyloid fibrils but did not form "star-like" appearances of unicentric plaques. All types of plaques were totally devoid of dystrophic neuritic elements. However, numerous microglial cells invaded them. The plaques observed by confocal laser microscope were of the same types as those analyzed by electron microscopy. Neuronal processes surrounding the plaques did not show typical features of neuroaxonal dystrophy.Entities:
Keywords: Chronic wasting disease – prion diseases; amyloid plaques – microglial cells
Mesh:
Year: 2017 PMID: 29105545 PMCID: PMC5786356 DOI: 10.1080/19336896.2017.1384109
Source DB: PubMed Journal: Prion ISSN: 1933-6896 Impact factor: 3.931