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Investigation of adhesion and mechanical properties of human glioma cells by single cell force spectroscopy and atomic force microscopy.

机译:通过单细胞力光谱和原子力显微镜研究人神经胶质瘤细胞的粘附和力学性能。

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摘要

Active cell migration and invasion is a peculiar feature of glioma that makes this tumor able to rapidly infiltrate into the surrounding brain tissue. In our recent work, we identified a novel class of glioma-associated-stem cells (defined as GASC for high-grade glioma--HG--and Gasc for low-grade glioma--LG) that, although not tumorigenic, act supporting the biological aggressiveness of glioma-initiating stem cells (defined as GSC for HG and Gsc for LG) favoring also their motility. Migrating cancer cells undergo considerable molecular and cellular changes by remodeling their cytoskeleton and cell interactions with surrounding environment. To get a better understanding about the role of the glioma-associated-stem cells in tumor progression, cell deformability and interactions between glioma-initiating stem cells and glioma-associated-stem cells were investigated. Adhesion of HG/LG-cancer cells on HG/LG-glioma-associated stem cells was studied by time-lapse microscopy, while cell deformability and cell-cell adhesion strengths were quantified by indentation measurements by atomic force microscopy and single cell force spectroscopy. Our results demonstrate that for both HG and LG glioma, cancer-initiating-stem cells are softer than glioma-associated-stem cells, in agreement with their neoplastic features. The adhesion strength of GSC on GASC appears to be significantly lower than that observed for Gsc on Gasc. Whereas, GSC spread and firmly adhere on Gasc with an adhesion strength increased as compared to that obtained on GASC. These findings highlight that the grade of glioma-associated-stem cells plays an important role in modulating cancer cell adhesion, which could affect glioma cell migration, invasion and thus cancer aggressiveness. Moreover this work provides evidence about the importance of investigating cell adhesion and elasticity for new developments in disease diagnostics and therapeutics.
机译:活跃的细胞迁移和侵袭是神经胶质瘤的特有特征,它使这种肿瘤能够迅速渗入周围的脑组织。在我们最近的工作中,我们确定了一类新型的神经胶质瘤相关干细胞(对于高级别神经胶质瘤定义为GASC – HG –对于低级别神经胶质瘤定义为Gasc – LG),尽管不是致癌的,但可以起到支持作用胶质瘤起始干细胞(定义为HG的GSC和LG的Gsc)的生物学攻击性也有利于它们的运动。迁移的癌细胞通过重塑细胞骨架和细胞与周围环境的相互作用而经历了相当大的分子和细胞变化。为了更好地了解神经胶质瘤相关干细胞在肿瘤进展中的作用,研究了细胞变形能力以及神经胶质瘤起始干细胞与神经胶质瘤相关干细胞之间的相互作用。通过延时显微镜研究了HG / LG-胶质瘤相关干细胞上HG / LG癌细胞的粘附,而原子力显微镜和单细胞力光谱通过压痕测量定量了细胞的可变形性和细胞粘附强度。我们的研究结果表明,对于HG和LG胶质瘤,癌症起始干细胞比神经胶质瘤相关干细胞更柔软,这与其肿瘤特征相符。 GSC在GASC上的粘合强度似乎明显低于Gsc在Gasc上的粘合强度。然而,与在GASC上获得的粘合强度相比,GSC可以在Gasc上扩散并牢固地粘合,其粘合强度更高。这些发现表明,神经胶质瘤相关干细胞的等级在调节癌细胞粘附中起着重要作用,这可能会影响神经胶质瘤细胞的迁移,侵袭并进而侵袭癌症。此外,这项工作提供了有关研究细胞粘附和弹性对于疾病诊断和治疗新进展的重要性的证据。

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