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首页> 外文期刊>Cancer genetics >First cloned human immortalized adipose derived mesenchymal stem-cell line with chimeric SS18-SSX1 gene (SS-iASC)
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First cloned human immortalized adipose derived mesenchymal stem-cell line with chimeric SS18-SSX1 gene (SS-iASC)

机译:首先将克隆人永生化脂肪衍生的间充质干细胞与嵌合SS18-SSX1基因(SS-IASC)

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The SS18-SSX chimeric gene is unique to synovial sarcoma. Multiple model systems including mouse cell lines expressing SS18-SSX , and genetically engineered mouse models of synovial sarcoma have been developed to elucidate the role of the chimeric gene in synovial sarcomagenesis. Although several cell lines stably expressing human SS18-SSX exist, there is an ongoing need for cell culture models enabling researchers to investigate the molecular mechanism of SS18-SSX action in a relevant cellular context. Here we report the establishment of a novel SS18-SSX1 -expressing cell line created from immortalized human adipose tissue-derived mesenchymal stem cells via lentiviral transduction of the chimeric gene. Our cell line, termed SS-iASC, has been characterized by karyotyping and cell line identification, and stable expression of SS18-SSX1 has been verified using real-time PCR (RT-PCR), nested PCR, immunofluorescence, and immunoblotting. Focal cytokeratin positivity characteristic of synovial sarcoma but no β-Catenin, Bcl-2 or cyclin D1 expression was observed in SS-iASC. The novel cell line expressing SS18-SSX1 on a human adipose-derived stromal cell background is expected to be helpful in addressing the question whether the chimeric gene alone is sufficient to trigger the formation of synovial sarcoma.
机译:SS18-SSX嵌合基因是滑膜肉瘤的独特性。已经开发了多种模型系统,包括表达SS18-SSX的小鼠细胞系,以及滑膜肉瘤的遗传工程鼠标模型,以阐明嵌合基因在滑膜SARComagenesis中的作用。尽管存在稳定表达人SS18-SSX的几种细胞系,但是需要持续需要进行细胞培养模型,使研究人员能够研究相关的细胞背景下的SS18-SSX作用的分子机制。在这里,我们报告了通过嵌合基因的慢病毒转导的由永生化的人脂肪组织衍生的间充质干细胞产生的新的SS18-SSX1 -Expressing细胞系。我们的细胞系已被称为SS-IASC,其特征在于核型化和细胞系鉴定,并且使用实时PCR(RT-PCR),嵌套的PCR,免疫荧光和免疫印迹已经验证了SS18-SSX1的稳定表达。在SS-IASC中观察到滑膜肉瘤,但没有β-catenin,Bcl-2或细胞周期蛋白D1表达的焦细胞角蛋白阳性特征。在人脂肪衍生的基质细胞背景上表达SS18-SSX1的新细胞系预计有助于解决单独的嵌合基因是否足以引发滑膜肉瘤的形成。

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