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Differentiation profile of brain tumor stem cells: a comparative study with neural stem cells

机译:脑肿瘤干细胞的分化特征:与神经干细胞的比较研究

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摘要

Understanding of the differentiation profile of brain tumor stem cells (BTSCs), the key ones among tumor cell population, through comparison with neural stem cells (NSCs) would lend insight into the origin of glioma and ultimately yield new approaches to fight this intractable disease. Here, we cultured and purified BTSCs from surgical glioma specimens and NSCs from human fetal brain tissue, and further analyzed their cellular biological behaviors, especially their differentiation property. As expected, NSCs differentiated into mature neural phenotypes. In the same differentiation condition, however, BTSCs exhibited distinguished differences. Morphologically, cells grew flattened and attached for the first week, but gradually aggregated and reformed floating tumor sphere thereafter. During the corresponding period, the expression rate of undifferentiated cell marker CD133 and nestin in BTSCs kept decreasing, but 1 week later, they regained ascending tendency. Interestingly, the differentiated cell markers GFAP and β-tubulinIII showed an expression change inverse to that of undifferentiated cell markers. Taken together, BTSCs were revealed to possess a capacity to resist differentiation, which actually represents the malignant behaviors of glioma.
机译:通过与神经干细胞(NSC)的比较,了解肿瘤细胞群中关键的脑肿瘤干细胞(BTSC)的分化概况,将有助于深入了解神经胶质瘤的起源,并最终产生抗击这种顽固性疾病的新方法。在这里,我们从外科神经胶质瘤标本中培养和纯化了BTSC,从人类胎儿脑组织中纯化了NSC,并进一步分析了它们的细胞生物学行为,特别是它们的分化特性。如预期的那样,NSC分化为成熟的神经表型。但是,在相同的分化条件下,BTSC表现出明显的差异。形态上,细胞在第一周生长扁平并附着,但此后逐渐聚集并重新形成漂浮的肿瘤球。在同一时期,未分化的细胞标志物CD133和巢蛋白在BTSCs中的表达率持续下降,但是1周后,它们又恢复了上升的趋势。有趣的是,分化的细胞标志物GFAP和β-微管蛋白III的表达变化与未分化的细胞标志物相反。综上所述,BTSCs具有抵抗分化的能力,实际上代表了神经胶质瘤的恶性行为。

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