Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29106
Title: Accumulation profiles of PrPSc in hemal nodes of naturally and experimentally scrapie-infected sheep
Authors: Dassanayake, Rohana P.
Truscott, Thomas C.
Zhuang, Dongyue
Schneider, David A.
O'Rourke, Katherine I.
Uludağ Üniversitesi/Veteriner Fakültesi/Patoloji Anabilim Dalı.
Özyiǧit, Musa Özgür
AAR-6478-2021
AAH-2873-2021
6507338060
Keywords: Veterinary sciences
Scrapie
Hemal nodes
Epitope mapping
Sheep
Prions
TSE
Transmissible spongiform encephalopathy
Blood-transfusion
Prion protein
Lymph-node
Preclinical diagnosis
Tissues
Cells
Ovine
Lymphocytes
Immunohistochemistry
Animalia
Bovidae
Ovis
Ovis aries
Issue Date: 19-Apr-2013
Publisher: Bmc
Citation: Dassanayake, R. P. vd. (2013). "Accumulation profiles of PrPSc in hemal nodes of naturally and experimentally scrapie-infected sheep". BMC Veterinary Research, 9.
Abstract: Background: In classical scrapie, the disease-associated abnormal isoform (PrPSc) of normal prion protein accumulates principally in the nervous system and lymphoid tissues of small ruminants. Lymph nodes traffic leukocytes via lymphatic and blood vasculatures but hemal nodes lack lymphatic vessels and thus traffic leukocytes only via the blood. Although PrPSc accumulation profiles are well-characterized in ovine lymphoid tissues, there is limited information on such profiles in hemal nodes. Therefore, the objective of this study was to compare the follicular accumulation of PrPSc within hemal nodes and lymph nodes by prion epitope mapping and western blot studies. Results: Our studies found that PrPSc accumulation in 82% of animals' abdominal hemal nodes when PrPSc is detected in both mesenteric and retropharyngeal lymph nodes collected from preclinical and clinical, naturally and experimentally (blood transfusion) scrapie-infected sheep representing all three major scrapie-susceptible Prnp genotypes. Abdominal hemal nodes and retropharyngeal lymph nodes were then used to analyze immune cell phenotypes and PrPSc epitope mapping by immunohistochemistry and PrPSc banding patterns by western blot. Similar patterns of PrPSc accumulation were detected within the secondary follicles of hemal nodes and retropharyngeal lymph nodes, where cellular labeling was mostly associated with macrophages and follicular dendritic cells. The pattern of PrPSc accumulation within hemal nodes and retropharyngeal lymph nodes also did not differ with respect to epitope mapping with seven mAbs (N-terminus, n = 4; globular domain, n = 2; C-terminus, n = 1) in all three Prnp genotypes. Western blot analysis of hemal node and retropharyngeal lymph node homogenates revealed identical three banding patterns of proteinase K resistant PrPSc. Conclusion: Despite the anatomical difference in leukocyte trafficking between lymph nodes and hemal nodes, the follicles of hemal nodes appear to process PrPSc similarly to lymph nodes.
URI: https://doi.org/10.1186/1746-6148-9-82
https://bmcvetres.biomedcentral.com/articles/10.1186/1746-6148-9-82
http://hdl.handle.net/11452/29106
ISSN: 1746-6148
Appears in Collections:Scopus
Web of Science

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