Enrichment of prion protein in exosomes derived from ovine cerebral spinal fluid

被引:169
作者
Vella, Laura J. [1 ,2 ,3 ]
Greenwood, Deanne L. V. [4 ]
Cappai, Roberto [2 ,3 ]
Scheerlinck, Jean-Pierre Y. [4 ]
Hill, Andrew F. [1 ,2 ,3 ]
机构
[1] Univ Melbourne, Dept Biochem & Mol Biol, Bio21 Mol Sci & Biotehcnol Inst, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Dept Pathol, Melbourne, Vic 3010, Australia
[3] Mental Hlth Res Inst, Parkville, Vic 3010, Australia
[4] Univ Melbourne, Sch Vet Sci, Ctr Anim Biotechnol, Melbourne, Vic 3010, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
prion; exosomes; cerebral spinal fluid;
D O I
10.1016/j.vetimm.2008.04.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Prion diseases are transmissible neurodegenerative disorders affecting humans and a wide variety of animal species including sheep and cattle. The transmissible agent, the prion, is an abnormally folded form (PrPSc) of the host encoded cellular prion protein (PrPC). Distribution of the prion protein in the fluids of species Susceptible to these diseases is of importance to human health and the iatrogenic spread of prion disease. Aside from blood which is confirmed to be a source of prion infectivity, it is Currently unclear which other body fluids harbor a significant transmission risk. In the Current study we examined two ovine fluids pseudo-afferent, lymph and cerebral spinal fluid (CSF), for the presence of exosomes and concurrent enrichment of the normal, cellular form of the prion protein (PrPC). Here we demonstrate the existence of exosomes in both pseudo-afferent lymph and CSF isolated from sheep. In the CSF derived exosomes we were able to show an enrichment of PrPC over Unfractionated CSF This experimental approach suggests that CSF derived exosomes could be Used as a novel means of detecting abnormal forms of the prion protein and provide an in vivo link between these vesicles and prion disease pathogenesis. (C) 2008 Published by Elsevier B.V.
引用
收藏
页码:385 / 393
页数:9
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