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Epithelial and endothelial expression of the green fluorescent protein reporter gene under the control of bovine prion protein (PrP) gene regulatory sequences in transgenic mice

机译:在牛病毒蛋白(PrP)基因调控序列控制下,绿色荧光蛋白报道基因在上皮和内皮中的表达

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摘要

The expression of the cellular form of the prion protein (PrPc) gene is required for prion replication and neuroinvasion in transmissible spongiform encephalopathies. The identification of the cell types expressing PrPc is necessary to understanding how the agent replicates and spreads from peripheral sites to the central nervous system. To determine the nature of the cell types expressing PrPc, a green fluorescent protein reporter gene was expressed in transgenic mice under the control of 6.9 kb of the bovine PrP gene regulatory sequences. It was shown that the bovine PrP gene is expressed as two populations of mRNA differing by alternative splicing of one 115-bp 5′ untranslated exon in 17 different bovine tissues. The analysis of transgenic mice showed reporter gene expression in some cells that have been identified as expressing PrP, such as cerebellar Purkinje cells, lymphocytes, and keratinocytes. In addition, expression of green fluorescent protein was observed in the plexus of the enteric nervous system and in a restricted subset of cells not yet clearly identified as expressing PrP: the epithelial cells of the thymic medullary and the endothelial cells of both the mucosal capillaries of the intestine and the renal capillaries. These data provide valuable information on the distribution of PrPc at the cellular level and argue for roles of the epithelial and endothelial cells in the spread of infection from the periphery to the brain. Moreover, the transgenic mice described in this paper provide a model that will allow for the study of the transcriptional activity of the PrP gene promoter in response to scrapie infection.
机译:在可传播的海绵状脑病中,ion病毒的复制和神经浸润需要required病毒蛋白(PrPc)基因的细胞形式的表达。鉴定表达PrPc的细胞类型对于了解药物如何从周围部位复制和扩散到中枢神经系统是必要的。为了确定表达PrPc的细胞类型的性质,在6.9kb的牛PrP基因调控序列的控制下,在转基因小鼠中表达了绿色荧光蛋白报道基因。结果表明,牛PrP基因表达为两个mRNA群体,它们通过在17种不同的牛组织中一个115 bp 5'非翻译外显子的选择性剪接而有所不同。对转基因小鼠的分析显示,报告基因在某些已被确定为表达PrP的细胞中表达,例如小脑浦肯野细胞,淋巴细胞和角质形成细胞。此外,在肠神经系统神经丛和尚未明确鉴定为表达PrP的细胞的有限子集中观察到绿色荧光蛋白的表达:胸腺髓质的上皮细胞和两种黏膜毛细血管的内皮细胞肠和肾毛细血管。这些数据提供了有关PrPc在细胞水平上分布的有价值的信息,并争辩了上皮细胞和内皮细胞在感染从外围扩散到大脑中的作用。而且,本文描述的转基因小鼠提供了一个模型,该模型将允许研究响应瘙痒病感染的PrP基因启动子的转录活性。

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