Biotech Business Unit, Incubation Center, artience Co., Ltd., 5-6-7 Chiyoda, Sakado-city, Saitama 350-0214, Japan.
Department of Bioengineering, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
ACS Appl Mater Interfaces. 2024 Aug 28;16(34):44575-44589. doi: 10.1021/acsami.4c10118. Epub 2024 Aug 19.
To control three-dimensional (3D) cell spheroid formation, it is well-known the surface physicochemical and mechanical properties of cell culture materials are important; however, the formation and function of 3D cells are still unclear. This study demonstrated the precise control of the formation of 3D cells and 3D cell functions using diblock copolymers containing different ratios of a zwitterionic trimethylamine -oxide group. The diblock copolymers were composed of poly(-butyl methacrylate) (PBMA) as the hydrophobic unit for surface coating on a cell culture dish and stabilization in water, and poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) as the precursor of -oxide. The zwitterionic -oxide converted from 0 to 100% using PDMAEMA. The wettability and surface zeta potential varied with different ratios of -oxide diblock copolymer-coated surfaces, and the amount of protein adsorbed in the cell culture medium decreased monotonically with increasing -oxide ratio. 3D cell spheroid formations were observed by seeding human umbilical cord mesenchymal stem cells (hUC-MSCs) in diblock copolymer-coated flat-bottom well plates, and the -oxide ratio was over 40%. The cells proliferated in two-dimensions (2D) and did not form spheroids when the -oxide ratio was less than 20%. Interestingly, the expression of undifferentiated markers of hUC-MSCs was higher on surfaces that adsorbed proteins to some extent and formed 50-150 μm spheroids in the range of 40-70% of -oxide ratio. We revealed that a moderately protein-adsorbed surface allows precise control of spheroid formation and undifferentiated 3D cells and has potential applications for high-quality spheroids in regenerative medicine and drug screening.
为了控制三维(3D)细胞球体的形成,众所周知细胞培养材料的表面物理化学和机械性能很重要;然而,3D 细胞的形成和功能仍不清楚。本研究使用含有不同比例两性离子氧化三甲胺基团的嵌段共聚物,展示了对 3D 细胞形成和 3D 细胞功能的精确控制。嵌段共聚物由聚(-甲基丙烯酸丁酯)(PBMA)作为疏水单元,用于细胞培养皿的表面涂层和在水中的稳定化,以及聚(2-(二甲氨基)乙基甲基丙烯酸酯)(PDMAEMA)作为氧化三甲胺的前体。通过 PDMAEMA 将氧化三甲胺的比例从 0 转换为 100%。具有不同氧化三甲胺嵌段共聚物涂层表面的润湿性和表面zeta 电位发生变化,并且细胞培养基中吸附的蛋白质量随着氧化三甲胺比例的增加而单调减少。通过将人脐带间充质干细胞(hUC-MSCs)接种在嵌段共聚物涂层的平底孔板中观察到 3D 细胞球体的形成,并且氧化三甲胺的比例超过 40%。当氧化三甲胺的比例小于 20%时,细胞在二维(2D)中增殖并且不形成球体。有趣的是,在某种程度上吸附蛋白质的表面上 hUC-MSCs 的未分化标志物的表达更高,并且在氧化三甲胺比例为 40-70%的范围内形成 50-150μm 的球体。我们揭示了适度吸附蛋白质的表面允许对球体形成和未分化的 3D 细胞进行精确控制,并且在再生医学和药物筛选中具有高质量球体的潜在应用。