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首页> 外文期刊>Histochemistry and cell biology >Recapitulating in vivo-like plasticity of glioma cell invasion along blood vessels and in astrocyte-rich stroma
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Recapitulating in vivo-like plasticity of glioma cell invasion along blood vessels and in astrocyte-rich stroma

机译:携带血管和富含星形胶质细胞侵袭的胶质瘤细胞侵袭的体内可塑性

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Diffuse invasion of glioma cells into the brain parenchyma leads to nonresectable brain tumors and poor prognosis of glioma disease. In vivo, glioma cells can adopt a range of invasion strategies and routes, by moving as single cells, collective strands and multicellular networks along perivascular, perineuronal and interstitial guidance cues. Current in vitro assays to probe glioma cell invasion, however, are limited in recapitulating the modes and adaptability of glioma invasion observed in brain parenchyma, including collective behaviours. To mimic in vivo-like glioma cell invasion in vitro, we here applied three tissue-inspired 3D environments combining multicellular glioma spheroids and reconstituted microanatomic features of vascular and interstitial brain structures. Radial migration from multicellular glioma spheroids of human cell lines and patient-derived xenograft cells was monitored using (1) reconstituted basement membrane/hyaluronan interfaces representing the space along brain vessels; (2) 3D scaffolds generated by multi-layered mouse astrocytes to reflect brain interstitium; and (3) freshly isolated mouse brain slice culture ex vivo. The invasion patterns in vitro were validated using histological analysis of brain sections from glioblastoma patients and glioma xenografts infiltrating the mouse brain. Each 3D assay recapitulated distinct aspects of major glioma invasion patterns identified in mouse xenografts and patient brain samples, including individually migrating cells, collective strands extending along blood vessels, and multicellular networks of interconnected glioma cells infiltrating the neuropil. In conjunction, these organotypic assays enable a range of invasion modes used by glioma cells and will be applicable for mechanistic analysis and targeting of glioma cell dissemination.
机译:弥漫性侵袭胶质瘤细胞进入脑进行实质导致不可识别的脑肿瘤和胶质瘤病的预后差。在体内,通过作为单细胞,集体股线和血管内和间隙指导提示作为单细胞,集体链和多细胞网络移动,可以采用一系列侵入策略和路线。然而,探测胶质瘤细胞侵袭的目前的体外测定受到限制,在重新携带脑部实质中观察到的胶质瘤侵袭的模式和适应性,包括集体行为。为了模仿体内的胶质瘤细胞侵袭,我们在这里施加了三种组织启发的3D环境,组合多细胞胶质瘤球状球体和重构血管和间质脑结构的微杀菌特征。使用(1)代表沿脑壳血管的空间的重构的基底膜/透明质酸细胞来监测来自人细胞系和患者衍生的异种移植细胞的多细胞胶质瘤球体的径向迁移; (2)多层小鼠星形胶质细胞产生的3D支架,以反映脑插孔; (3)新鲜孤立的小鼠脑切片文化前体内。使用来自胶质母细胞瘤患者的脑切片的组织学分析和胶质瘤异种移植物的组织学分析验证了体外侵袭模式。每个3D测定重新携带在小鼠异种移植物和患者脑样品中鉴定的主要胶质瘤侵袭模式的独特方面,包括单独迁移细胞,沿血管延伸的集体股,以及渗透神经潜入的互联胶质瘤细胞的多细胞网络。结合,这些有机型测定能够使胶质瘤细胞使用的一系列侵入模式,并且适用于机械分析和胶质瘤细胞传播的靶向。

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