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Endothelial cell transdifferentiation of human glioma stem progenitor cells in vitro.

机译:人脑胶质瘤干祖细胞内皮细胞的体外分化。

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The transdifferentiation of normal stem cells in many kinds of tissues or organs has been studied. However, whether glioma stem cells can transdifferentiate is seldom reported. Meanwhile, the mechanism of angiogenesis in tumors is in disputations, and it is still unknown that whether glioma stem/progenitor cells (GSPCs) participate into angiogenesis in glioma. In this study, we cultivated GSPCs in endothelial differentiation medium for 10 days and found they present to be the typical "flagstone" appearance of vascular endothelial cell (VEC); when cultured on Matrigel, GSPCs gradually formed tubular-like structures in vitro, and cells, which formed the tubular-like structures, showed similar ultrastructural characteristics of VEC under a transmission electron microscope. Furthermore, when cultured in hypoxia or oxygen-glucose deprivation for 4h, GSPCs transcribed and expressed molecular markers of VEC, including CD31, CD34 and vWF. These results indicated that GSPCs could participate into angiogenesis of glioma by transdifferentiating into VEC-like cells.
机译:已经研究了正常干细胞在多种组织或器官中的转分化。但是,很少报道神经胶质瘤干细胞是否可以分化。同时,肿瘤中血管生成的机制尚存争议,并且胶质瘤干/祖细胞(GSPCs)是否参与神经胶质瘤的血管生成仍是未知的。在这项研究中,我们在内皮分化培养基中培养了GSPC 10天,发现它们是血管内皮细胞(VEC)的典型“石板”外观。当在基质胶上培养时,GSPCs在体外逐渐形成管状结构,并且在透射电子显微镜下,形成管状结构的细胞表现出相似的VEC超微结构特征。此外,当在缺氧或缺氧葡萄糖条件下培养4h时,GSPC转录并表达VEC的分子标记,包括CD31,CD34和vWF。这些结果表明,GSPCs可以通过转分化为VEC样细胞来参与神经胶质瘤的血管生成。

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