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首页> 外文期刊>Acta Histochemica: Zeitschrift fur Histologische Topochemie >Differentiation potential of the cells in the macula flava of the human vocal fold mucosa
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Differentiation potential of the cells in the macula flava of the human vocal fold mucosa

机译:人声粘粘膜黄斑粘膜中细胞的分化潜力

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The latest research suggests cells in the maculae flavae located at both ends of the lamina propria of the human vocal fold mucosa have sternness. This study investigated the differentiation potential of the cells in the maculae flavae of the human vocal fold mucosa. Four normal human adult vocal folds from surgical specimens were used. After extraction of the anterior maculae flavae located at the anterior end of the lamina propria of the human vocal fold mucosa under microscope, the maculae flavae were minced, cultured and proliferated in mesenchymal stern cell growth medium and morphological features were assessed. Cell surface markers were detected using flow cytometry. Cell differentiation into adipogenic, chondrogenic and osteogenic lineages was performed. Cell's differentiation potential was assessed using a human pluripotent stem cell functional identification kit and immunohistochemistry. Subcultured cells formed a colony-forming unit. Subcultured cells expressed CD90, CD105 and CD73 and lacked expression of CD45, CD34, CD11b, CD19 and HLA-DR. They differentiated into adipogenic, chondrogenic and osteogenic lineages. Consequently, the cell features in the maculae flavae meet the minimal criteria defining mesenchymal stromal cells. In addition, subcultured cells differentiated into ectoderm, mesoderm and endoderm and expressed stage-specific embryonic antigen 3 (SSEA-3). The results of this study are consistent with the hypothesis that the cells in the maculae flavae in the lamina propria of the human vocal fold mucosa are putative stem cells.
机译:最新研究表明,位于Lamina Propria的两端的黄斑黄皮中的细胞具有沉默的。本研究研究了人声折粘膜的黄斑黄藻中细胞的分化潜力。使用来自外科手术标本的四个正常人体成人声带。在显微镜下萃取位于人声倍粘膜的椎板丙胶的前端前端的前后黄斑,切碎,在间充质船尾细胞生长培养基中培养和增殖并评估形态特征。使用流式细胞术检测细胞表面标志物。进行细胞分化成脂肪发生,软骨形成和骨质发生谱系。使用人类多能干细胞功能识别试剂盒和免疫组化评估细胞的分化电位。亚培养细胞形成菌落形成单元。递推细胞表达CD90,CD105和CD73,缺乏CD45,CD34,CD11B,CD19和HLA-DR的表达。它们分化为脂肪原性,软骨性和骨质发生谱系。因此,黄斑黄脂中的细胞特征满足了定义间充质基质细胞的最小标准。另外,将亚培养细胞分化为外胚层,中胚层和内胚层,表达阶段特异性胚胎抗原3(SSEA-3)。该研究的结果与人声折粘膜的椎板丙虫中的黄斑黄脂中的细胞具有稳定的干细胞。

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