Institute for Macromolecular Chemistry, University of Freiburg, 79104 Freiburg, Germany.
BIOSS Centre for Biological Signalling Studies, University of Freiburg, 79104 Freiburg, Germany.
Int J Mol Sci. 2022 Jul 25;23(15):8188. doi: 10.3390/ijms23158188.
In multicellular organisms, cells are organized in a 3-dimensional framework and this is essential for organogenesis and tissue morphogenesis. Systems to recapitulate 3D cell growth are therefore vital for understanding development and cancer biology. Cells organized in 3D environments can evolve certain phenotypic traits valuable to physiologically relevant models that cannot be accessed in 2D culture. Cellular spheroids constitute an important aspect of in vitro tumor biology and they are usually prepared using the hanging drop method. Here a 3D printed approach is demonstrated to fabricate bespoke hanging drop devices for the culture of tumor cells. The design attributes of the hanging drop device take into account the need for high-throughput, high efficacy in spheroid formation, and automation. Specifically, in this study, custom-fit, modularized hanging drop devices comprising of inserts (Q-serts) were designed and fabricated using fused filament deposition (FFD). The utility of the Q-serts in the engineering of unicellular and multicellular spheroids-synthetic tumor microenvironment mimics (STEMs)-was established using human (cancer) cells. The culture of spheroids was automated using a pipetting robot and bioprinted using a custom bioink based on carboxylated agarose to simulate a tumor microenvironment (TME). The spheroids were characterized using light microscopy and histology. They showed good morphological and structural integrity and had high viability throughout the entire workflow. The systems and workflow presented here represent a user-focused 3D printing-driven spheroid culture platform which can be reliably reproduced in any research environment and scaled to- and on-demand. The standardization of spheroid preparation, handling, and culture should eliminate user-dependent variables, and have a positive impact on translational research to enable direct comparison of scientific findings.
在多细胞生物中,细胞组织在三维框架中,这对器官发生和组织形态发生至关重要。因此,能够再现 3D 细胞生长的系统对于理解发育和癌症生物学至关重要。在 3D 环境中组织的细胞可以进化出某些表型特征,这些特征对于生理相关模型非常有价值,而在 2D 培养中无法获得。细胞球体是体外肿瘤生物学的一个重要方面,通常使用悬滴法制备。这里展示了一种 3D 打印方法,用于制造用于培养肿瘤细胞的定制悬滴装置。悬滴装置的设计属性考虑了高通量、高效形成球体以及自动化的需求。具体而言,在这项研究中,使用熔融沉积成型(FFF)设计并制造了定制的、模块化的悬滴装置,包括插入物(Q-sert)。使用人类(癌症)细胞证明了 Q-sert 在单细胞和多细胞球体-合成肿瘤微环境模拟物(STEM)的工程中的用途。使用移液机器人自动化培养球体,并使用基于羧基化琼脂糖的定制生物墨水进行生物打印,以模拟肿瘤微环境(TME)。使用光学显微镜和组织学对球体进行了表征。它们在整个工作流程中表现出良好的形态和结构完整性,并且具有高活力。这里呈现的系统和工作流程代表了一个以用户为中心的 3D 打印驱动的球体培养平台,可以在任何研究环境中可靠地复制,并按需扩展。球体制备、处理和培养的标准化应消除用户依赖的变量,并对转化研究产生积极影响,从而能够直接比较科学发现。