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微流控重编程将人类体细胞诱导为多能性状态。

Microfluidic reprogramming to pluripotency of human somatic cells.

机构信息

Shanghai Institute for Advanced Immunochemical Studies (SIAIS), ShanghaiTech University, Shanghai, China.

Department of Industrial Engineering, University of Padova, Padova, Italy.

出版信息

Nat Protoc. 2019 Mar;14(3):722-737. doi: 10.1038/s41596-018-0108-4. Epub 2019 Feb 26.

DOI:10.1038/s41596-018-0108-4
PMID:30809022
Abstract

Human induced pluripotent stem cells (hiPSCs) have a number of potential applications in stem cell biology and regenerative medicine, including precision medicine. However, their potential clinical application is hampered by the low efficiency, high costs, and heavy workload of the reprogramming process. Here we describe a protocol to reprogram human somatic cells to hiPSCs with high efficiency in 15 d using microfluidics. We successfully downscaled an 8-d protocol based on daily transfections of mRNA encoding for reprogramming factors and immune evasion proteins. Using this protocol, we obtain hiPSC colonies (up to 160 ± 20 mean ± s.d (n = 48)) in a single 27-mm microfluidic chamber) 15 d after seeding ~1,500 cells per independent chamber and under xeno-free defined conditions. Only ~20 µL of medium is required per day. The hiPSC colonies extracted from the microfluidic chamber do not require further stabilization because of the short lifetime of mRNA. The high success rate of reprogramming in microfluidics, under completely defined conditions, enables hundreds of cells to be simultaneously reprogrammed, with an ~100-fold reduction in costs of raw materials compared to those for standard multiwell culture conditions. This system also enables the generation of hiPSCs suitable for clinical translation or further research into the reprogramming process.

摘要

人类诱导多能干细胞(hiPSCs)在干细胞生物学和再生医学,包括精准医学中具有许多潜在的应用。然而,其潜在的临床应用受到重编程过程效率低、成本高和工作量大的限制。在这里,我们描述了一种使用微流控技术在 15 天内高效将人体细胞重编程为 hiPSCs 的方案。我们成功地将基于每天转染用于重编程因子和免疫逃逸蛋白的 mRNA 的 8 天方案进行了小型化。使用该方案,我们在接种每孔~1500 个细胞后 15 天内(n=48),在单个 27-mm 微流控室中获得 hiPSC 集落(最高 160±20 平均值±s.d),并且在无动物成分的定义条件下进行。每天仅需要约 20 µL 的培养基。由于 mRNA 的寿命短,从微流控室中提取的 hiPSC 集落不需要进一步稳定。微流控技术在完全定义的条件下具有高重编程成功率,能够同时对数百个细胞进行重编程,与标准多孔培养条件相比,原材料成本降低了约 100 倍。该系统还能够生成适合临床转化或进一步研究重编程过程的 hiPSCs。

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