Role of gut macrophages in mice orally contaminated with scrapie or BSE

被引:47
作者
Maignien, T
Shakwed, M
Calvo, P
Marcé, D
Salès, N
Fattal, E
Deslys, JP
Couvreur, P [1 ]
Lasmezas, CI
机构
[1] Univ Paris Sud, Ctr Etudes Pharmaceut, UMR 8612, CNRS, F-92296 Chatenay Malabry, France
[2] CEA, Serv Neurovirol, CRSSA, Fontenay Aux Roses, France
[3] Univ Caen, UFR Sci Pharmaceut, F-14032 Caen, France
关键词
transmissible spongiform encephalopaties; macrophage-suicide technique; clodronate; Peyer's patches; intestinal uptake; nano- and microparticles;
D O I
10.1016/j.ijpharm.2005.02.042
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
While there is a growing consensus on the understanding of the propagation pathways after oral infection of transmissible spongiform encephalopathy (TSE) agents and even if the central role of follicular dendritic cells is identified, little is known about the key players in the first steps of the infection and about the site of the disease development. We investigated the role of gut macrophages, which are capable of capturing aggregates of the prion protein. PLGA particles containing clodronate were designed in order to be orally administered and to target Peyer's patches for inducing gut-associated macrophages suicide in mice. Mice were subsequently infected with scrapie or BSE by the oral route. It was found that the efficacy of macrophage suppression in the Peyer's patches correlated well with an earlier appearance of PrPres in these formations and with a higher amount of PrPres at a later stage of the infection. Thus, the capture of infectious particles that have crossed the epithelial gut barrier and their elimination by macrophages seems to be a key event to restrict the amount of agent initiating the infection. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:293 / 304
页数:12
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