PRP PROTEIN IS ASSOCIATED WITH FOLLICULAR DENDRITIC CELLS OF SPLEENS AND LYMPH-NODES IN UNINFECTED AND SCRAPIE-INFECTED MICE

被引:206
作者
MCBRIDE, PA
EIKELENBOOM, P
KRAAL, G
FRASER, H
BRUCE, ME
机构
[1] MRC,NEUROPATHOGENESIS UNIT,EDINBURGH EH9 3JF,SCOTLAND
[2] VRIJE UNIV AMSTERDAM,VAKGRP PSYCHIAT,1075 BG AMSTERDAM,NETHERLANDS
[3] FREE UNIV AMSTERDAM,FAC MED,DEPT CELL BIOL,DIV HISTOL,1081 BT AMSTERDAM,NETHERLANDS
关键词
SCRAPIE; PRP; FOLLICULAR DENDRITIC CELLS;
D O I
10.1002/path.1711680412
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Abnormal forms of a host protein, PrP, accumulate in the central nervous system in scrapie-affected animals. Here, PrP protein was detected immunocytochemically in tissue sections of spleen, lymph node, Peyer's patches, thymus, and pancreas from uninfected mice and from mice infected with a range of mouse-passaged scrapie strains and bovine spongiform encephalopathy (BSE). In the spleen, lymph node and Peyer's patches, PrP-positive cells were identified as follicular dendritic cells (FDC) by their location, appearance, and immune complex trapping function, whereas in the thymus they appeared to be two types of stromal cells: interdigitating cells (IDC) and cortical epithelial cells. In pancreas, PrP-containing cells were confined to the islets of Langerhans. Although the distribution of PrP immunolabelling was the same in tissues from scrapie-affected and uninfected mice, there was evidence that PrP accumulated in abnormal forms in FDC of infected mice. If, as is likely, PrP is essential for agent replication, our results suggest that FDC are the site of scrapie and BSE replication in the spleen and lymph node.
引用
收藏
页码:413 / 418
页数:6
相关论文
共 33 条
[1]  
ARMSTRONG JA, 1984, LANCET, V2, P370
[2]   DENDRITIC CELLS OF THE MOUSE RECOGNIZED BY 2 MONOCLONAL-ANTIBODIES [J].
BREEL, M ;
MEBIUS, RE ;
KRAAL, G .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1987, 17 (11) :1555-1559
[3]   PRECISE TARGETING OF THE PATHOLOGY OF THE SIALOGLYCOPROTEIN, PRP, AND VACUOLAR DEGENERATION IN MOUSE SCRAPIE [J].
BRUCE, ME ;
MCBRIDE, PA ;
FARQUHAR, CF .
NEUROSCIENCE LETTERS, 1989, 102 (01) :1-6
[4]   THE DISEASE CHARACTERISTICS OF DIFFERENT STRAINS OF SCRAPIE IN SINC CONGENIC MOUSE LINES - IMPLICATIONS FOR THE NATURE OF THE AGENT AND HOST CONTROL OF PATHOGENESIS [J].
BRUCE, ME ;
MCCONNELL, I ;
FRASER, H ;
DICKINSON, AG .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :595-603
[5]   INVITRO EXPRESSION IN EUKARYOTIC CELLS OF A PRION PROTEIN GENE CLONED FROM SCRAPIE-INFECTED MOUSE-BRAIN [J].
CAUGHEY, B ;
RACE, RE ;
VOGEL, M ;
BUCHMEIER, MJ ;
CHESEBRO, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (13) :4657-4661
[6]   PATHOGENESIS OF MOUSE SCRAPIE - DISTRIBUTION OF AGENT IN THE PULP AND STROMA OF INFECTED SPLEENS [J].
CLARKE, MC ;
KIMBERLIN, RH .
VETERINARY MICROBIOLOGY, 1984, 9 (03) :215-225
[7]   CHANGES IN THE LOCALIZATION OF BRAIN PRION PROTEINS DURING SCRAPIE INFECTION [J].
DEARMOND, SJ ;
MOBLEY, WC ;
DEMOTT, DL ;
BARRY, RA ;
BECKSTEAD, JH ;
PRUSINER, SB .
NEUROLOGY, 1987, 37 (08) :1271-1280
[8]   NONLYMPHOID CELLS IN THE SPLENIC WHITE PULP [J].
DIJKSTRA, CD ;
KRAAL, G .
RESEARCH IN IMMUNOLOGY, 1991, 142 (04) :325-328
[9]  
DIJKSTRA CD, 1985, IMMUNOLOGY, V55, P23
[10]  
DOI S, 1988, J GEN VIROL, V69, P955, DOI 10.1099/0022-1317-69-4-955