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Migrating intestinal dendritic cells transport PrPSc from the gut
205
Citations
31
References
2002
Year
Creutzfeldt-jakob DiseaseImmunologyImmune RegulationPathologyImmune SystemImmunotherapyCellular PhysiologySheep ScrapieNatural ScrapieImmunopathologyNeuroimmunologyCell SignalingIntestinal Dendritic CellsAutoimmune DiseaseCell TraffickingBovine Spongiform EncephalopathyAutoimmunityCell BiologySignal TransductionPathogenesisGut BarrierMedicine
Bovine spongiform encephalopathy, variant Creutzfeldt-Jakob disease (vCJD) and possibly also sheep scrapie are orally acquired transmissible spongiform encephalopathies (TSEs). TSE agents usually replicate in lymphoid tissues before they spread into the central nervous system. In mouse TSE models PrP(c)-expressing follicular dendritic cells (FDCs) resident in lymphoid germinal centres are essential for replication, and in their absence neuroinvasion is impaired. Disease-associated forms of PrP (PrP(Sc)), a biochemical marker for TSE infection, also accumulate on FDCs in the lymphoid tissues of patients with vCJD and sheep with natural scrapie. TSE transport mechanisms between gut lumen and germinal centres are unknown. Migratory bone marrow-derived dendritic cells (DCs), entering the intestinal wall from blood, sample antigens from the gut lumen and carry them to mesenteric lymph nodes. Here we show that DCs acquire PrP(Sc) in vitro, and transport intestinally administered PrP(Sc) directly into lymphoid tissues in vivo. These studies suggest that DCs are a cellular bridge between the gut lumen and the lymphoid TSE replicative machinery.
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