1 Department of Biomedical Engineering, University of Minnesota , Minneapolis, Minnesota.
2 Department of Mechanical Engineering, University of Minnesota , Minneapolis, Minnesota.
Tissue Eng Part C Methods. 2018 May;24(5):289-299. doi: 10.1089/ten.TEC.2017.0531. Epub 2018 Mar 28.
Inadequate preservation methods of human induced pluripotent stem cells (hiPSCs) have impeded efficient reestablishment of cell culture after the freeze-thaw process. In this study, we examined roles of the cooling rate, seeding temperature, and difference between cell aggregates (3-50 cells) and single cells in controlled rate freezing of hiPSCs. Intracellular ice formation (IIF), post-thaw membrane integrity, cell attachment, apoptosis, and cytoskeleton organization were evaluated to understand the different freezing responses between hiPSC single cells and aggregates, among cooling rates of 1, 3, and 10°C/min, and between seeding temperatures of -4°C and -8°C. Raman spectroscopy images of ice showed that a lower seeding temperature (-8°C) did not affect IIF in single cells, but significantly increased IIF in aggregates, suggesting higher sensitivity of aggregates to supercooling. In the absence of IIF, Raman images showed greater variation of dimethyl sulfoxide concentration across aggregates than single cells, suggesting cryoprotectant transport limitations in aggregates. The ability of cryopreserved aggregates to attach to culture substrates did not correlate with membrane integrity for the wide range of freezing parameters, indicating inadequacy of using only membrane integrity-based optimization metrics. Lower cooling rates (1 and 3°C/min) combined with higher seeding temperature (-4°C) were better at preventing IIF and preserving cell function than a higher cooling rate (10°C/min) or lower seeding temperature (-8°C), proving the seeding temperature range of -7°C to -12°C from literature to be suboptimal. Unique f-actin cytoskeletal organization into a honeycomb-like pattern was observed in postpassage and post-thaw colonies and correlated with successful reestablishment of cell culture.
人类诱导多能干细胞(hiPSC)的保存方法不当,阻碍了冻融后细胞培养的有效重建。在这项研究中,我们研究了冷却速率、接种温度以及细胞聚集体(3-50 个细胞)和单细胞之间的差异在 hiPSC 控制速率冷冻中的作用。通过评估细胞内冰形成(IIF)、冻融后细胞膜完整性、细胞附着、细胞凋亡和细胞骨架组织来了解 hiPSC 单细胞和聚集体之间的不同冷冻反应、冷却速率为 1°C、3°C 和 10°C/min 以及接种温度为-4°C 和-8°C。冰的拉曼光谱图像表明,较低的接种温度(-8°C)不会影响单细胞中的 IIF,但会显著增加聚集体中的 IIF,这表明聚集体对过冷的敏感性更高。在没有 IIF 的情况下,拉曼图像显示 DMSO 浓度在聚集体中的变化大于单细胞,这表明聚集体中存在抗冻剂传输限制。冷冻聚集体附着到培养基质的能力与膜完整性不相关,对于广泛的冷冻参数范围,这表明仅使用基于膜完整性的优化指标是不充分的。与较高的冷却速率(10°C/min)或较低的接种温度(-8°C)相比,较低的冷却速率(1°C 和 3°C/min)与较高的接种温度(-4°C)结合更能防止 IIF 和保存细胞功能,证明文献中的-7°C 至-12°C 的接种温度范围是不理想的。在传代后和冻融后菌落中观察到独特的 f-肌动蛋白细胞骨架组织呈蜂窝状,并与细胞培养的成功重建相关。