Dalir Abdolahinia Elaheh, Jafari Behzad, Parvizpour Sepideh, Barar Jaleh, Nadri Samad, Omidi Yadollah
Department of Medical Biotechnology, Zanjan University of Medical Sciences, Zanjan, Iran.
Research Center for Pharmaceutical Nanotechnology, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran.
Bioimpacts. 2021;11(2):111-117. doi: 10.34172/bi.2021.18. Epub 2020 Nov 2.
Cell aggregation of three-dimensional (3D) culture systems (the so-called spheroids) are designed as platform to represent more accurately the environment for drug discovery by using semi-solid media. The uniform multicellular tumor spheroids can be generated based on the interaction of cells with extracellular matrix (ECM) macromolecules such as collagen and integrin. This study aimed to investigate the possible interactions between the cellulose family and collagen using both and approaches. The 3D microtissue of JIMT-1 cells was generated using hanging drop method to study the effects of charge and viscosity of the medium containing cellulose family. To determine the mode of interaction between cellulose derivatives (CDs) and collagen-integrin, docking analysis and molecular simulation were further performed using open source web servers and chemical simulations (GROMACS), respectively. The results confirmed that the addition of CDs into the 3D medium can promote the formation of solid spheroids, where methylcellulose (MC) yielded uniform spheroids compared to carboxymethyl cellulose (CMC). Moreover, the computational analysis showed that MC interacted with both integrin and collagen, while sodium carboxymethyl cellulose (NaCMC) only interacted with collagen residues. The stated different behaviors in the 3D culture formation and collagen interaction were found in the physicochemical properties of CDs. Based on and findings, MC is suggested as an important ECM-mimicking entity that can support the semi-solid medium and promote the formation of the uniform spheroid in the 3D culture.
三维(3D)培养系统(即所谓的球体)中的细胞聚集被设计为一个平台,通过使用半固体培养基更准确地模拟药物发现的环境。基于细胞与细胞外基质(ECM)大分子(如胶原蛋白和整合素)的相互作用,可以生成均匀的多细胞肿瘤球体。本研究旨在使用实验和计算方法研究纤维素家族与胶原蛋白之间可能的相互作用。使用悬滴法生成JIMT-1细胞的3D微组织,以研究含有纤维素家族的培养基的电荷和粘度的影响。为了确定纤维素衍生物(CDs)与胶原蛋白-整合素之间的相互作用模式,分别使用开源网络服务器和化学模拟(GROMACS)进一步进行对接分析和分子模拟。结果证实,将CDs添加到3D培养基中可以促进固体球体的形成,其中甲基纤维素(MC)与羧甲基纤维素(CMC)相比产生均匀的球体。此外,计算分析表明,MC与整合素和胶原蛋白都相互作用,而羧甲基纤维素钠(NaCMC)仅与胶原蛋白残基相互作用。在CDs的物理化学性质中发现了3D培养形成和胶原蛋白相互作用方面所述的不同行为。基于实验和计算结果,MC被认为是一种重要的模拟ECM的实体,可以支持半固体培养基并促进3D培养中均匀球体的形成。