Expression of PrPC on cellular components of sheep blood
- 1 May 2005
- journal article
- Published by Microbiology Society in Journal of General Virology
- Vol. 86 (5) , 1571-1579
- https://doi.org/10.1099/vir.0.80561-0
Abstract
PrPC, a glycosylphosphatidylinositol-linked glycoprotein, plays a central role in the pathogenesis of transmissible spongiform encephalopathies (TSEs), undergoing a conformational alteration to the disease-associated isoform, commonly designated PrPSc. PrPC is expressed in many tissues other than the nervous system, although its precise function(s) remains unclear. It has previously been demonstrated that TSEs can be transmitted by blood transfusion in sheep. The aim of this work was to identify which components of blood carried the infection. As an initial step, the distribution of PrPC on cellular components of sheep blood was examined to identify potential targets for infection. Cell-surface expression of PrPC was found only on peripheral blood mononuclear cells (PBMCs); however, platelets also contained significant amounts of intracellular PrPC. The level of PrPC expressed on the cell surface of PBMCs was influenced by PrP genotype, with the highest levels found in scrapie-susceptible VRQ/VRQ sheep and the lowest levels in scrapie-resistant ARR/ARR sheep. In susceptible sheep, PrPC was expressed at varying levels on all major subsets of PBMCs, with the highest levels on the CD21+ subset of B cells, and PrP expression was upregulated dramatically on CD21+ B cells in some scrapie-infected sheep.Keywords
This publication has 42 references indexed in Scilit:
- Comparative analysis of normal prion protein expression on human, rodent, and ruminant blood cells by using a panel of prion antibodiesTransfusion, 2002
- Follicular dendritic cells in TSE pathogenesisImmunology Today, 2000
- Distribution of cell-associated prion protein in normal adult blood determined by flow cytometryBritish Journal of Haematology, 1999
- Further studies of blood infectivity in an experimental model of transmissible spongiform encephalopathy, with an explanation of why blood components do not transmit Creutzfeldt‐Jakob disease in humansTransfusion, 1999
- The distribution of infectivity in blood components and plasma derivatives in experimental models of transmissible spongiform encephalopathyTransfusion, 1998
- PrP-expressing tissue required for transfer of scrapie infectivity from spleen to brainNature, 1997
- Can Creutzfeldt-Jakob disease be transmitted by transfusion?Current Opinion in Hematology, 1995
- 6.8 Identification of monoclonal antibodies specific for bovine leukocyte common antigen (CD45) together with a novel broadly expressed leukocyte differentiation antigen, BoWC11Veterinary Immunology and Immunopathology, 1993
- Nearly ubiquitous tissue distribution of the scrapie agent precursor proteinNeurology, 1992
- Identification of a Protein That Purifies with the Scrapie PrionScience, 1982