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Establishment and Characterization of Choroid Plexus Carcinoma Cell Lines: Connection between Choroid Plexus and Immune Systems

机译:脉络丛癌细胞系的建立和表征:脉络丛与免疫系统之间的联系

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摘要

Murine choroid plexus cell lines were produced from choroid plexus carcinoma generated in transgenic mice harboring the viral oncogene simian virus 40 large tumor antigen under transcriptional control of an intronic enhancer region from the human immunoglobulin heavy chain (IgH) gene. Two morphologically distinct cell lines have been cloned. These established cell lines retained the characteristics of choroid plexus cells in that they expressed such choroid plexus cell marker or related proteins as transthyretin and α2‐macroglobulin. They were tumorigenic in nude mice. In the cell lines, the μA and μB (HE2) motifs within the IgH intronic enhancer were active and we also demonstrated the existence of the proteins binding to these motifs, suggesting a potential link between the choroid plexus and immune systems. It is considered that these binding proteins act as trans‐activators for the enhancer and may belong to the class of ETS‐related proteins. These cell lines and xenografts should be useful materials for analyses of choroid plexus functions.
机译:鼠脉络丛细胞系由脉络丛癌产生,该脉络丛癌是在人免疫球蛋白重链(IgH)基因的内含子增强子区域的转录控制下携带病毒致癌基因猿猴病毒40大肿瘤抗原的转基因小鼠中产生的。已经克隆了两种形态上不同的细胞系。这些建立的细胞系保留了脉络丛细胞的特征,因为它们表达了脉络丛细胞标志物或相关蛋白,如运甲状腺素蛋白和α2-巨球蛋白。它们在裸鼠中具有致瘤性。在细胞系中,IgH内含子增强子中的μA和μB(HE2)基序是活跃的,我们还证明了与这些基序结合的蛋白质的存在,表明脉络丛和免疫系统之间存在潜在的联系。这些结合蛋白被认为是增强子的反式激活剂,可能属于ETS相关蛋白。这些细胞系和异种移植物应该是分析脉络丛功能的有用材料。

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