Rocchi Mara S, Anderson Mary-Jo, Eaton Samantha L, Hamilton Scott, Finlayson Jeanie, Steele Philip, Barclay G Robin, Chianini Francesca
Moredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik, Scotland EH26 0PZ, UK.
Vet Immunol Immunopathol. 2007 Apr 15;116(3-4):172-81. doi: 10.1016/j.vetimm.2007.01.012. Epub 2007 Jan 31.
PrP(c) (cellular prion protein, CD230) expression by subpopulations of lymphoid cells has been widely investigated in a variety of species, possibly because of the possible link between transmissible spongiform encephalopathies (TSE) transmission and blood transfusion. However, the role of the immune cells in the transmission of the disease is still unclear. Here we describe the optimisation and standardisation of a three-colour staining procedure to detect PrP in association with phenotypic and activation markers in ovine immune cells. We demonstrate a reproducible, flexible and sensitive method and that the combination of isotype-specific antibodies and Fab fragments is feasible. To our knowledge, this is the first report of such labelling of ovine cells. Using this method, we were able to detect differences in levels of PrP expression between blood and lymph node cells of the same animal, and considerable variability between animals. Moreover, we were able to explore possible associations between PrP expression and cellular activation and to identify cell subsets with different labelling patterns. We are currently employing this approach to evaluate variations in immunological parameters during experimental infection in sheep.
由于传染性海绵状脑病(TSE)传播与输血之间可能存在联系,淋巴样细胞亚群的PrP(c)(细胞朊蛋白,CD230)表达已在多种物种中得到广泛研究。然而,免疫细胞在疾病传播中的作用仍不清楚。在此,我们描述了一种三色染色程序的优化和标准化方法,用于检测绵羊免疫细胞中与表型和激活标记相关的PrP。我们展示了一种可重复、灵活且灵敏的方法,并且同型特异性抗体和Fab片段的组合是可行的。据我们所知,这是关于绵羊细胞此类标记的首次报道。使用该方法,我们能够检测同一动物血液和淋巴结细胞之间PrP表达水平的差异,以及不同动物之间的显著变异性。此外,我们能够探索PrP表达与细胞激活之间的可能关联,并识别具有不同标记模式的细胞亚群。我们目前正在采用这种方法来评估绵羊实验性感染期间免疫参数的变化。