Department of Biomedical Engineering, School of Medicine, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Tsinghua University, Haidian District, Beijing, 100084, China.
School of Biological Science and Medical Engineering, Beihang University, Haidian District, Beijing, 100191, China.
Lab Chip. 2016 Aug 2;16(16):2996-3006. doi: 10.1039/c6lc00331a.
Understanding the complex regulatory network that determines stem cell fates requires a high-throughput platform that can generate a large number of precisely controlled microenvironments representing multiple factors for stem cell culture and analysis. Here, we developed a superhydrophobic microwell array chip on which the culture conditions in each microwell can be spontaneously isolated by a grafted layer of superhydrophobic polymers. Simple steps for medium exchange were developed to facilitate the on-chip culture of both adherent and non-adherent cells for up to six days without compromising cell viability and functionality. The culture conditions in each microwell were facilely manipulated using a robotic spotter. Stem cell niches combining soluble factors, extracellular matrices and microtopographic cues were generated on a single 512-well SMARchip and their combinatorial effects on the fate of mouse Oct4-EGFP iPSCs were systematically probed. We observed significant differences in iPSC pluripotency and proliferation between adherent flat and suspended spherical cultures on our platform, which might provide insights into improvement of stem cell technologies.
理解决定干细胞命运的复杂调控网络需要一个高通量平台,该平台能够产生大量精确控制的微环境,代表用于干细胞培养和分析的多种因素。在这里,我们开发了一种超疏水微井阵列芯片,在该芯片上,通过接枝的超疏水聚合物层可以自发地隔离每个微井中的培养条件。开发了简单的培养基交换步骤,以促进长达六天的贴壁和非贴壁细胞在芯片上的培养,而不会损害细胞活力和功能。使用机器人点样器可以轻松地操纵每个微井中的培养条件。在单个 512 孔 SMARchip 上生成了结合可溶性因子、细胞外基质和微形貌线索的干细胞龛,系统地探测了它们对小鼠 Oct4-EGFP iPSCs 命运的组合效应。我们观察到在我们的平台上,贴壁的平面和悬浮的球体培养之间的 iPSC 多能性和增殖存在显著差异,这可能为改进干细胞技术提供了思路。