首页> 美国卫生研究院文献>PLoS Clinical Trials >Exosome-Producing Follicle Associated Epithelium Is Not Involved in Uptake of PrPd from the Gut of Sheep (Ovis aries): An Ultrastructural Study
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Exosome-Producing Follicle Associated Epithelium Is Not Involved in Uptake of PrPd from the Gut of Sheep (Ovis aries): An Ultrastructural Study

机译:产卵泡相关的卵泡上皮不参与从羊肠(羊)肠道摄取PrPd:超微结构研究

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摘要

In natural or experimental oral scrapie infection of sheep, disease associated prion protein (PrPd) often first accumulates in Peyer's patch (PP) follicles. The route by which infectivity reaches the follicles is unknown, however, intestinal epithelial cells may participate in intestinal antigenic presentation by delivering exosomes as vehicles of luminal antigens. In a previous study using an intestinal loop model, following inoculation of scrapie brain homogenate, inoculum associated PrPd was detected by light microscopy shortly (15 minutes to 3.5 hours) after inoculation in the villous lacteals and sub-mucosal lymphatics. No PrPd was located within the follicle-associated epithelium (FAE), sub-FAE domes or the PP follicles. To evaluate this gut loop model and the transportation routes in more detail, we used electron microscopy (EM) to study intestinal tissues exposed to scrapie or control homogenates for 15 minutes to 10 days. In addition, immuno-EM was used to investigate whether exosomes produced in the FAE may possess small amounts of PrPd that were not detectable by light microscopy. This study showed that the integrity of the intestinal epithelium was sustained in the intestinal loop model. Despite prominent transcytotic activity and exosome release from the FAE of the ileal PP in sheep, these structures were not associated with transportation of PrPd across the mucosa. The study did not determine how infectivity reaches the follicles of PPs. The possibility that the infectious agent is transported across the FAE remains a possibility if it occurs in a form that is undetectable by the methods used in this study. Infectivity may also be transported via lymph to the blood and further to all other lymphoid tissues including the PP follicles, but the early presence of PrPd in the PP follicles during scrapie infection argues against such a mechanism.
机译:在绵羊的自然或实验性口腔瘙痒病感染中,与疾病相关的ion病毒蛋白(PrP d )通常会先在Peyer's patch(PP)卵泡中积累。感染力到达卵泡的途径尚不清楚,但是,肠上皮细胞可能通过递送外泌体作为腔内抗原的载体而参与肠内抗原呈递。在先前使用肠loop模型的研究中,接种了瘙痒性脑匀浆后,在绒毛状乳腺和亚乳腺接种后不久(15分钟至3.5小时)通过光学显微镜检测了与接种物相关的PrP d 粘膜淋巴管在与卵泡相关的上皮(FAE),亚FAE穹顶或PP卵泡中未发现PrP d 。为了更详细地评估此肠道回路模型和运输途径,我们使用电子显微镜(EM)研究暴露于瘙痒病或对照匀浆的肠组织15分钟至10天。另外,使用免疫EM技术来研究FAE中产生的外泌体是否可能具有少量的PrP d ,而这是光学显微镜无法检测到的。该研究表明肠上皮的完整性在肠loop模型中得以维持。尽管绵羊具有显着的跨细胞活性和回肠PP的FAE释放外来体,但这些结构与PrP d 在整个粘膜中的运输无关。该研究尚未确定感染性如何到达PPs的卵泡。如果传染源以本研究中使用的方法无法检测到的形式发生,则仍有可能通过FAE进行传染。感染力也可能通过淋巴转移到血液,甚至进一步转移到包括PP卵泡在内的所有其他淋巴组织,但是在瘙痒病感染期间PP卵泡中PrP d 的早期存在反对了这种机制。

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