Prion strains are differentially released through the exosomal pathway

被引:36
作者
Arellano-Anaya, Zaira E. [1 ,2 ]
Huor, Alvina [1 ,2 ]
Leblanc, Pascal [3 ]
Lehmann, Sylvain [4 ,5 ]
Provansal, Monique [4 ,5 ]
Raposo, Graca [6 ]
Andreoletti, Olivier [1 ,2 ]
Vilette, Didier [1 ,2 ]
机构
[1] INRA, UMR 1225, IHAP, F-31076 Toulouse, France
[2] Univ Toulouse, INP, ENVT, IHAP,UMR 1225, F-31076 Toulouse, France
[3] Ecole Normale Super Lyon, LBMC, Equipe Differenciat Neuromusculaire, CNRS,UMR 5239, F-69364 Lyon 07, France
[4] Univ Montpellier I, INSERM, Ctr Hosp Univ Montpellier,U1040, IMRB,Physiopathol Diagnost & Therapie Cellulaire, Montpellier, France
[5] CNRS, Inst Genet Humaine, UPR 1142, Montpellier, France
[6] Inst Curie, CNRS, UMR 144, Struct & Membrane Compartments,Cell & Tissue Imag, F-75248 Paris 05, France
关键词
Prion release; Cell models; Exosome; Extracellular vesicle; Prion spiking; TSE agent; SHEEP SCRAPIE; B-LYMPHOCYTES; IN-VITRO; INFECTIVITY; BLOOD; CELLS; TRANSMISSION; PROPAGATION; VESICLES; AGENT;
D O I
10.1007/s00018-014-1735-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell-to-cell transfer of prions is a crucial step in the spreading of prion infection through infected tissue. At the cellular level, several distinct pathways including direct cell-cell contacts and release of various types of infectious extracellular vesicles have been described that may potentially lead to infection of na < ve cells. The relative contribution of these pathways and whether they may vary depending on the prion strain and/or on the infected cell type are not yet known. In this study we used a single cell type (RK13) infected with three different prion strains. We showed that in each case, most of the extracellular prions resulted from active cell secretion through the exosomal pathway. Further, quantitative analysis of secreted infectivity indicated that the proportion of prions eventually secreted was dramatically dependent on the prion strain. Our data also highlight that infectious exosomes secreted from cultured cells might represent a biologically pertinent material for spiking experiments. Also discussed is the appealing possibility that abnormal PrP from different prion strains may differentially interact with the cellular machinery to promote secretion.
引用
收藏
页码:1185 / 1196
页数:12
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