摘要
Transmissible spongiform encephalopathies (TSEs) are slowly progressive and fatal neurodegenerative diseases affecting man and animals. They are caused by pathological isoforms (PrPSc) of the host-encoded cellular prion protein (PrPC). There are two crucial factors for the initiation of infection, namely host cells PrPC expression and sufficient sequence homology between the PrPSc to which the animal is exposed and its own PrPC. In acquired TSEs, the gastrointestinal tract (GIT) is the main prion entry site. Hence, it is of paramount importance to an understanding of the early pathogenesis of prion infections, to characterize the GIT cell types constitutively expressing PrPC. Twenty-three mice were utilized, including wild-type (WT), Prnp knock-out (KO), and PrPC-overexpressing (tga20/tga20) animals, of 20–30 g in weight and of either sex. In all three groups of mice, PrPC-immunoreactivity (IR), along with glial fibrillary acidic protein (GFAP)-IR and synaptophysin (Syn)-IR were investigated by means of indirect immunofluorescence in wholemount preparations from several gut regions, from duodenum to rectum. In WT mice, PrPC-IR and GFAP-IR co-localization was observed in enteric glial cells (EGCs) from all intestinal segments. PrPC-overexpressing mice showed a stronger PrPC-IR in EGCs, whereas the same cells exhibited no PrPC-IR in Prnp-KO mice.