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A transfectant RK13 cell line permissive to classical caprine scrapie prion propagation

机译:允许经典的山羊瘙痒病pr病毒繁殖的转染RK13细胞系

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ABSTRACT To assess scrapie infectivity associated with caprine-origin tissues, bioassay can be performed using kids, lambs or transgenic mice expressing caprine or ovine prion (PRNP) alleles, but the incubation periods are fairly long. Although several classical ovine scrapie prion permissive cell lines with the ability to detect brain-derived scrapie prion have been available, no classical caprine scrapie permissive cell line is currently available. Therefore, the aims of this study were to generate a rabbit kidney epithelial cell line (RK13) stably expressing caprine wild-type PRNP (cpRK13) and then to assess permissiveness of cpRK13 cells to classical caprine scrapie prion propagation. The cpRK13 and plasmid control RK13 (pcRK13) cells were incubated with brain-derived classical caprine scrapie inocula prepared from goats or ovinized transgenic mice (Tg338, express ovine VRQ allele) infected with caprine scrapie. Significant PrPSc accumulation, which is indicative of scrapie prion propagation, was detected by TSE ELISA and immunohistochemistry in cpRK13 cells inoculated with classical caprine scrapie inocula. Western blot analysis revealed the typical proteinase K-resistant 3 PrPres isoforms in the caprine scrapie prion inoculated cpRK13 cell lysate. Importantly, PrPSc accumulation was not detected in similarly inoculated pcRK13 cells, whether by TSE ELISA, immunohistochemistry, or western blot. These findings suggest that caprine scrapie prions can be propagated in cpRK13 cells, thus this cell line may be a useful tool for the assessment of classical caprine prions in the brain tissues of goats.
机译:摘要为了评估与山羊源组织相关的瘙痒病感染性,可以使用表达山羊或pr病毒(PRNP)等位基因的孩子,羔羊或转基因小鼠进行生物测定,但是潜伏期相当长。尽管已有几种具有检测脑源性瘙痒病pr病毒能力的经典羊瘙痒病pr病毒允许细胞系,但目前尚无经典的山羊瘙痒病per允许细胞系。因此,本研究的目的是产生稳定表达山羊野生型PRNP(cpRK13)的兔肾上皮细胞系(RK13),然后评估cpRK13细胞对经典山羊瘙痒病pr病毒繁殖的允许性。将cpRK13和质粒对照RK13(pcRK13)细胞与脑衍生的经典山羊瘙痒病接种物孵育,该接种物是用山羊或经山羊瘙痒病感染的转基因小鼠(Tg338,表达绵羊VRQ等位基因)制备的。通过TSE ELISA和免疫组织化学,在接种经典山羊瘙痒病接种物的cpRK13细胞中检测到PrPSc大量积累,这表明瘙痒病pr病毒的繁殖。蛋白质印迹分析揭示了在山羊刮scrap病毒感染的cpRK13细胞裂解物中典型的蛋白酶K抗性3 PrPres亚型。重要的是,无论是通过TSE ELISA,免疫组织化学还是蛋白质印迹,在类似接种的pcRK13细胞中均未检测到PrPSc积累。这些发现表明,山羊瘙痒病病毒可在cpRK13细胞中繁殖,因此该细胞系可能是评估山羊脑组织中经典山羊rine病毒的有用工具。

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