In transmitted prion diseases the immune system supports the replication and the propagation of the pathogenic agent (PrPSc). DCs, which are mobile cells present in large numbers within lymph organs, are suspected to carry prions through the lymphoid system and to transfer them towards the peripheral nervous system. In this study, C57Bl/6 mice were orally inoculated with PrPSc (scrapie strain 139A) and sacrificed at the preclinical stages of the disease. Immunolabelled cryosections of Peyer's patches were analysed by confocal microscopy. Membrane prion protein expression was studied by flow cytometry. In Peyer's patches (PP), dissected at day one and day 105 after oral exposure to scrapie, we observed an increased population of DCs localise...
Transmissible spongiform encephalopathies are fatal neurodegenerative diseases. Infection by the ora...
Although the alimentary tract has been suggested as the most likely portal of entry in natural scra...
Prion infectivity and its molecular marker, the pathological prion protein PrPSc, accumulate in the ...
Transmissible spongiform encephalopathies (TSEs) or prion diseases are infectious neurological disor...
International audiencePeripherally acquired transmissible spongiform encephalopathies display striki...
Transmissible spongiform encephalopathies (scrapie, BSE, Kuru) develop as CNS diseases after long in...
International audienceTransmissible spongiform encephalopathies display long incubation periods at t...
International audienceTransmissible spongiform encephalopathies display long incubation periods at t...
International audienceTransmissible spongiform encephalopathies display long incubation periods at t...
The involvement of immune cells in prion capture and transport to lymphoid tissues still remains unc...
The involvement of immune cells in prion capture and transport to lymphoid tissues still remains unc...
The cellular prion protein (PrPC) is a sialoglycoprotein anchored to the external surface of cells b...
The cellular prion protein (PrPC) is a sialoglycoprotein anchored to the external surface of cells b...
Using the severe combined immunodeficiency (SCID) mouse model, we investigated the requirement of th...
Transmissible spongiform encephalopathies (TSEs), or prion diseases, are fatal neurodegenerative dis...
Transmissible spongiform encephalopathies are fatal neurodegenerative diseases. Infection by the ora...
Although the alimentary tract has been suggested as the most likely portal of entry in natural scra...
Prion infectivity and its molecular marker, the pathological prion protein PrPSc, accumulate in the ...
Transmissible spongiform encephalopathies (TSEs) or prion diseases are infectious neurological disor...
International audiencePeripherally acquired transmissible spongiform encephalopathies display striki...
Transmissible spongiform encephalopathies (scrapie, BSE, Kuru) develop as CNS diseases after long in...
International audienceTransmissible spongiform encephalopathies display long incubation periods at t...
International audienceTransmissible spongiform encephalopathies display long incubation periods at t...
International audienceTransmissible spongiform encephalopathies display long incubation periods at t...
The involvement of immune cells in prion capture and transport to lymphoid tissues still remains unc...
The involvement of immune cells in prion capture and transport to lymphoid tissues still remains unc...
The cellular prion protein (PrPC) is a sialoglycoprotein anchored to the external surface of cells b...
The cellular prion protein (PrPC) is a sialoglycoprotein anchored to the external surface of cells b...
Using the severe combined immunodeficiency (SCID) mouse model, we investigated the requirement of th...
Transmissible spongiform encephalopathies (TSEs), or prion diseases, are fatal neurodegenerative dis...
Transmissible spongiform encephalopathies are fatal neurodegenerative diseases. Infection by the ora...
Although the alimentary tract has been suggested as the most likely portal of entry in natural scra...
Prion infectivity and its molecular marker, the pathological prion protein PrPSc, accumulate in the ...