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Investigation of Tumor Cell Behaviors on a Vascular Microenvironment-Mimicking Microfluidic Chip

机译:模拟血管微环境的微流控芯片上肿瘤细胞行为的研究

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The extravasation of tumor cells is a key event in tumor metastasis. However, the mechanism underlying tumor cell extravasation remains unknown, mainly hindered by obstacles from the lack of complexity of biological tissues in conventional cell culture, and the costliness and ethical issues of in vivo experiments. Thus, a cheap, time and labor saving, and most of all, vascular microenvironment-mimicking research model is desirable. Herein, we report a microfluidic chip-based tumor extravasation research model which is capable of simultaneously simulating both mechanical and biochemical microenvironments of human vascular systems and analyzing their synergistic effects on the tumor extravasation. Under different mechanical conditions of the vascular system, the tumor cells (HeLa cells) had the highest viability and adhesion activity in the microenvironment of the capillary. The integrity of endothelial cells (ECs) monolayer was destroyed by tumor necrosis factor-α (TNF-α) in a hemodynamic background, which facilitated the tumor cell adhesion, this situation was recovered by the administration of platinum nanoparticles (Pt-NPs). This model bridges the gap between cell culture and animal experiments and is a promising platform for studying tumor behaviors in the vascular system.
机译:肿瘤细胞的外渗是肿瘤转移中的关键事件。然而,肿瘤细胞外渗的机制仍是未知的,主要是由于常规细胞培养中缺乏生物组织的复杂性以及体内实验的昂贵和伦理问题而产生的障碍。因此,需要廉价,节省时间和劳力的方法,最重要的是,模仿血管微环境的研究模型。本文中,我们报道了一种基于微流体芯片的肿瘤外渗研究模型,该模型能够同时模拟人体血管系统的机械和生化微环境,并分析它们对肿瘤外渗的协同作用。在血管系统的不同机械条件下,肿瘤细胞(HeLa细胞)在毛细管的微环境中具有最高的生存力和粘附活性。在血液动力学背景下,肿瘤坏死因子-α(TNF-α)破坏了内皮细胞(ECs)单层的完整性,从而促进了肿瘤细胞的粘附,这种情况通过给予铂纳米颗粒(Pt-NPs)得以恢复。该模型弥补了细胞培养与动物实验之间的空白,是研究血管系统肿瘤行为的有前途的平台。

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