Leibniz Research Laboratories for Biotechnology and Artificial Organs (LEBAO), Germany.
REBIRTH Cluster of Excellence, Hannover Medical School, Hannover, Germany.
Stem Cells Transl Med. 2021 Jul;10(7):1063-1080. doi: 10.1002/sctm.20-0453. Epub 2021 Mar 4.
To harness the full potential of human pluripotent stem cells (hPSCs) we combined instrumented stirred tank bioreactor (STBR) technology with the power of in silico process modeling to overcome substantial, hPSC-specific hurdles toward their mass production. Perfused suspension culture (3D) of matrix-free hPSC aggregates in STBRs was applied to identify and control process-limiting parameters including pH, dissolved oxygen, glucose and lactate levels, and the obviation of osmolality peaks provoked by high density culture. Media supplements promoted single cell-based process inoculation and hydrodynamic aggregate size control. Wet lab-derived process characteristics enabled predictive in silico modeling as a new rational for hPSC cultivation. Consequently, hPSC line-independent maintenance of exponential cell proliferation was achieved. The strategy yielded 70-fold cell expansion in 7 days achieving an unmatched density of 35 × 10 cells/mL equivalent to 5.25 billion hPSC in 150 mL scale while pluripotency, differentiation potential, and karyotype stability was maintained. In parallel, media requirements were reduced by 75% demonstrating the outstanding increase in efficiency. Minimal input to our in silico model accurately predicts all main process parameters; combined with calculation-controlled hPSC aggregation kinetics, linear process upscaling is also enabled and demonstrated for up to 500 mL scale in an independent bioreactor system. Thus, by merging applied stem cell research with recent knowhow from industrial cell fermentation, a new level of hPSC bioprocessing is revealed fueling their automated production for industrial and therapeutic applications.
为了充分发挥人类多能干细胞(hPSCs)的潜力,我们将仪器化搅拌槽生物反应器(STBR)技术与计算机模拟过程建模的强大功能相结合,克服了 hPSC 大规模生产的大量特定障碍。在 STBR 中,对无基质 hPSC 聚集体进行灌注悬浮培养(3D),以识别和控制包括 pH 值、溶解氧、葡萄糖和乳酸水平在内的过程限制参数,并避免高密度培养引起的渗透压峰值。培养基补充剂促进了单细胞接种和水动力聚集体大小控制。实验室湿处理获得的过程特性使预测性计算建模成为 hPSC 培养的新合理方法。因此,实现了 hPSC 系独立的指数细胞增殖维持。该策略在 7 天内实现了 70 倍的细胞扩增,达到了无与伦比的 35×10^6 个细胞/ml 的密度,相当于 150ml 规模下的 52.5 亿个 hPSC,同时保持了多能性、分化潜能和核型稳定性。同时,将培养基需求降低了 75%,证明效率显著提高。我们的计算模型的最小输入可以准确预测所有主要过程参数;结合计算控制的 hPSC 聚集动力学,还可以实现线性过程放大,在独立的生物反应器系统中放大到 500ml 规模。因此,通过将应用于干细胞的研究与工业细胞发酵的最新知识相结合,揭示了 hPSC 生物加工的新水平,为其自动化生产用于工业和治疗应用提供了动力。