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Bone morphogenetic proteins and retinoic acid induce human endogenous retrovirus HERV-K expression in NT2D1 human embryonal carcinoma cells

机译:骨形态发生蛋白和维甲酸诱导人内源性逆转录病毒HERV-K在NT2D1人胚癌细胞中的表达

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摘要

Expression of the HERV-K human endogenous retrovirus is very low in normal and tumor tissue, but is readily detected in testicular germ cell tumors (TGCT). NT2D1 human embryonal carcinoma cells represent in vitro models for the stem cells of TGCT, and can be differentiated by treatment with bone morphogenetic proteins (BMP) or retinoic acid (RA). In a search for BMP target genes in NT2D1 cells, HERV-K was identified as an early BMP and RA target. It was shown that HERV-K expression was induced upontreatment of NT2D1 cells with BMP or with RA, but not with activin or transforming growth factor (TGF)-#beta#. Induction of HERV-K expression was rapid but transient, with transcripts becoming undetectable in differentiated NT2D1 cultures. Thus NT2D1 cells provide a suitable in vitro system for the study of the factors controlling HERV-K expression during cellular differentiation, which may play a role in HERV-K expression in TGCT.
机译:HERV-K人内源性逆转录病毒在正常组织和肿瘤组织中的表达非常低,但在睾丸生殖细胞肿瘤(TGCT)中很容易检测到。 NT2D1人类胚胎癌细胞代表TGCT干细胞的体外模型,可以通过用骨形态发生蛋白(BMP)或视黄酸(RA)处理来区分。在NT2D1细胞中寻找BMP靶基因时,HERV-K被鉴定为早期BMP和RA靶。结果表明,用BMP或RA而不是激活素或转化生长因子(TGF)-#beta#处理NT2D1细胞后,即可诱导HER​​V-K表达。 HERV-K表达的诱导是快速但短暂的,在分化的NT2D1培养物中无法检测到转录本。因此,NT2D1细胞为研究细胞分化过程中控制HERV-K表达的因子提供了合适的体外系统,这些因子可能在TGCT中的HERV-K表达中起作用。

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