The MOE Key Laboratory of Spectrochemical Analysis & Instrumentation, Key Laboratory for Chemical Biology of Fujian Province, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University , Xiamen 361005, People's Republic of China.
Anal Chem. 2014 Mar 4;86(5):2789-97. doi: 10.1021/ac500088m. Epub 2014 Feb 18.
Microfabricated devices are suitable for single-cell analysis due to their high throughput, compatible dimensions and controllable microenvironment. However, existing devices for single-cell culture and analysis encounter some limitations, such as nutrient depletion, random cell migration and complicated fluid shear influence. Moreover, most of the single-cell culture and analysis devices are based on 2D cell culture conditions, even though 3D cell culture methods have been demonstrated to better mimic the real cell microenvironment in vivo. To solve these problems, herein we develop a microcollagen gel array (μCGA) based approach for high-throughput long-term single-cell culture and single-cell analysis under 3D culture conditions. Type-I collagen, a well-established 3D cell culture medium, was used as the scaffold for 3D cell growth. A 2 × 2 cm PDMS chip with 10 000 μCGA units was fabricated to encapsulate thousands of single cells in less than 15 min. Single cells were able to be confined and survive in μCGA units for more than 1 month. The capability of large-scale and long-term single-cell 3D culture under open culture conditions allows us to study cellular proliferation heterogeneity and drug cytotoxicity at the single-cell level. Compared with existing devices for single-cell analysis, μCGA solves the problems of nutrient depletion and random cellular migration, avoids the influence of complicated fluid shear, and mimics the real 3D growth environment in vivo, thereby providing a feasible 3D long-term single-cell culture method for single-cell analysis and drug screening.
微纳加工设备由于其高通量、兼容的尺寸和可控制的微环境,非常适合单细胞分析。然而,现有的单细胞培养和分析设备存在一些局限性,例如营养物质耗尽、细胞随机迁移和复杂的流体剪切力影响。此外,大多数单细胞培养和分析设备都是基于 2D 细胞培养条件,尽管 3D 细胞培养方法已经被证明可以更好地模拟体内真实的细胞微环境。为了解决这些问题,我们开发了一种基于微胶原凝胶阵列(μCGA)的方法,用于在 3D 培养条件下进行高通量的长期单细胞培养和单细胞分析。I 型胶原作为一种成熟的 3D 细胞培养基,被用作 3D 细胞生长的支架。制作了一个 2×2cm 的 PDMS 芯片,上面有 10000 个μCGA 单元,可以在不到 15 分钟的时间内封装数千个单细胞。单细胞可以在 μCGA 单元中被限制和存活超过 1 个月。在开放培养条件下进行大规模和长期的单细胞 3D 培养的能力使我们能够在单细胞水平上研究细胞增殖异质性和药物细胞毒性。与现有的单细胞分析设备相比,μCGA 解决了营养物质耗尽和细胞随机迁移的问题,避免了复杂流体剪切力的影响,并模拟了体内真实的 3D 生长环境,从而为单细胞分析和药物筛选提供了一种可行的 3D 长期单细胞培养方法。