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Core/shell multicellular spheroids on chitosan as in vitro 3D coculture tumor models

机译:壳聚糖上的核/壳多细胞球体作为体外3D共培养肿瘤模型

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An ideal in vitro drug screening model is important for the drug development. In addition to monoculture systems, 3 dimensional (3D) coculture systems are extensively used to simulate the in vivo tumor microenvironment as cell-cell and cell-extracellular matrix interactions within the tumor tissues can be mimicked. In this study, in vitro 3D suspension coculture multicellular spheroids with core/shell cell distribution were developed on chitosan-coated surfaces. Based on the characteristic of chitosan inhibiting cell adhesion, SW620 (colon cancer cell line), 3A6 (mesenchymal stem-like cell line) and Hs68 (foreskin fibroblast line) cells could aggregate to form 3D coculture spheroids with intimate cell contacts. When cells were cocultured on chitosan, 3A6 and Hs68 cells always located in the core of spheroids and were completely enveloped by SW620 cells due to their N-cadherin protein expression following the differential adhesion hypothesis. The core cells could be the feeder layers to stimulate the shell SW620 cells to enhance their mitochondria activity. Moreover, 3D coculture core/shell multicellular spheroids could enhance the resistance of SW620 cells against the cytotoxicity effect of chemotherapy drugs. To sum up, based on the specificity of the core/shell coculture multicellular spheroids, a novel in vitro tumor model was proposed in this study.
机译:理想的体外药物筛选模型对于药物开发很重要。除单一培养系统外,由于可以模拟肿瘤组织内的细胞-细胞和细胞-细胞外基质相互作用,因此广泛使用3维(3D)共培养系统来模拟体内肿瘤微环境。在这项研究中,在壳聚糖包被的表面上开发了具有核/壳细胞分布的体外3D悬浮共培养多细胞球体。根据壳聚糖抑制细胞粘附的特性,SW620(结肠癌细胞系),3A6(间充质干细胞样细胞系)和Hs68(包皮成纤维细胞系)细胞可以聚集形成与细胞紧密接触的3D共培养球体。当将细胞在壳聚糖上共培养时,3A6和Hs68细胞始终位于球体的核心,并且由于差异粘附假设后它们的N-钙粘蛋白蛋白表达而被SW620细胞完全包裹。核心细胞可能是刺激壳SW620细胞以增强其线粒体活性的饲养层。此外,3D共培养核/壳多细胞球体可以增强SW620细胞对化疗药物的细胞毒性作用的抵抗力。综上所述,基于核/壳共培养多细胞球体的特异性,本研究提出了一种新型的体外肿瘤模型。

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