NR AJVC
AU Raeber,A.J.; Montrasio,F.; Hegyi,I.; Frigg,R.; Klein,M.A.; Aguzzi,A.; Weissmann,C.
TI Studies on prion replication in spleen
QU Developmental Immunology 2001; 8(3-4): 291-304
PT journal article
AB Some of the early events following scrapie infection take place in the lymphoreticular system (LRS) and result in significant replication of prions in lymphoid organs. The identity of the cells in the LRS that produce prions and their role in neuroinvasion are still unknown. We find that in the spleen of scrapie-infected mice, prions are associated with T and B cells and to a somewhat lesser degree with the stroma, which contains the follicular dendritic cells (FDC's); curiously, no infectivity was found in lymphocytes from blood of the same mice. Thus, splenic lymphocytes either replicate prions or acquire them from another source. Studies on PrP knockout mice with ectopic expression of PrP restricted to only B or T lymphocytes suggest that neither of these by themselves are competent for prion replication. To determine whether B and T cells are able to pick up prions from other sources, irradiated wild-type mice were reconstituted with PrP-deficient lymphohaematopoietic stem cells. Following intraperitoneal inoculation of these mice, no infectivity was found on splenic lymphocytes whereas the stroma (comprising the radiation-resistant, PrP-expressing FDC's) contained prions. These results imply that splenic lymphocytes can acquire prions, possibly from FDC's, but only if they express PrP.
MH Animal; Immunohistochemistry; Mice; Mice, Knockout; Models, Immunological; Organ Specificity; Prions/*biosynthesis/genetics/physiology; Promoter Regions (Genetics); Scrapie/immunology/*metabolism/transmission; Spleen/immunology/*metabolism; Support, Non-U.S. Gov't; Transcription, Genetic
AD Institute of Neuropathology, University Hospital, Zürich, Switzerland. raeber@cytos.com
SP englisch
PO England