Automated real-time monitoring of human pluripotent stem cell aggregation in stirred tank reactors

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作者
Ivo Schwedhelm
Daniela Zdzieblo
Antje Appelt-Menzel
Constantin Berger
Tobias Schmitz
Bernhard Schuldt
Andre Franke
Franz-Josef Müller
Ole Pless
Thomas Schwarz
Philipp Wiedemann
Heike Walles
Jan Hansmann
机构
[1] University Hospital Würzburg,Translational Center for Regenerative Therapies
[2] Department Tissue Engineering and Regenerative Medicine (TERM),undefined
[3] Fraunhofer Institute for Silicate Research ISC,undefined
[4] University Hospital Schleswig-Holstein,undefined
[5] Department of Psychiatry and Psychotherapy,undefined
[6] University Hospital Schleswig-Holstein,undefined
[7] Institute of Clinical Molecular Biology,undefined
[8] Fraunhofer Institute for Molecular Biology and Applied Ecology IME,undefined
[9] Mannheim University of Applied Sciences,undefined
[10] Institute of Molecular and Cell Biology,undefined
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摘要
The culture of human induced pluripotent stem cells (hiPSCs) at large scale becomes feasible with the aid of scalable suspension setups in continuously stirred tank reactors (CSTRs). Innovative monitoring options and emerging automated process control strategies allow for the necessary highly defined culture conditions. Next to standard process characteristics such as oxygen consumption, pH, and metabolite turnover, a reproducible and steady formation of hiPSC aggregates is vital for process scalability. In this regard, we developed a hiPSC-specific suspension culture unit consisting of a fully monitored CSTR system integrated into a custom-designed and fully automated incubator. As a step towards cost-effective hiPSC suspension culture and to pave the way for flexibility at a large scale, we constructed and utilized tailored miniature CSTRs that are largely made from three-dimensional (3D) printed polylactic acid (PLA) filament, which is a low-cost material used in fused deposition modelling. Further, the monitoring tool for hiPSC suspension cultures utilizes in situ microscopic imaging to visualize hiPSC aggregation in real-time to a statistically significant degree while omitting the need for time-intensive sampling. Suitability of our culture unit, especially concerning the developed hiPSC-specific CSTR system, was proven by demonstrating pluripotency of CSTR-cultured hiPSCs at RNA (including PluriTest) and protein level.
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