Abstract
ObjectiveFor optimized expansion of human‐induced pluripotent stem cells (hiPSCs) with regards to clinical applications, we investigated the influence of the inoculum density on the expansion procedure in 3D hollow‐fibre bioreactors.Materials and MethodsAnalytical‐scale bioreactors with a cell compartment volume of 3 mL or a large‐scale bioreactor with a cell compartment volume of 17 mL were used and inoculated with either 10 × 106 or 50 × 106 hiPSCs. Cells were cultured in bioreactors over 15 days; daily measurements of biochemical parameters were performed. At the end of the experiment, the CellTiter‐Blue® Assay was used for culture activity evaluation and cell quantification. Also, cell compartment sections were removed for gene expression and immunohistochemistry analysis.ResultsThe results revealed significantly higher values for cell metabolism, cell activity and cell yields when using the higher inoculation number, but also a more distinct differentiation. As large inoculation numbers require cost and time‐extensive pre‐expansion, low inoculation numbers may be used preferably for long‐term expansion of hiPSCs. Expansion of hiPSCs in the large‐scale bioreactor led to a successful production of 5.4 × 109 hiPSCs, thereby achieving sufficient cell amounts for clinical applications.ConclusionsIn conclusion, the results show a significant effect of the inoculum density on cell expansion, differentiation and production of hiPSCs, emphasizing the importance of the inoculum density for downstream applications of hiPSCs. Furthermore, the bioreactor technology was successfully applied for controlled and scalable production of hiPSCs for clinical use.
Highlights
Since the application of hiPSCs in the medical field requires large cell quantities at high‐quality standards, it is of great interest to evaluate fac‐ tors that influence hiPSC expansion in 3D culture systems
The effect of the inoculum density on the hiPSC expansion procedure, cell differentiation and the cell yield was investigated in this study
Analytical‐scale (3 mL) bioreactors inoculated with 50 × 106 cells (AS 50) consumed glucose faster than analytical‐scale bioreactors inoculated with 10 × 106 cells (AS 10), and growth stagnated signifi‐ cantly earlier
Summary
The expression data for the second marker of the ectodermal lineage, NEFL (Figure 3G), showed the strongest increase for embryoid bodies, with expression values being significantly higher compared with AS 10 and AS 50 as well as the 2D cultures (P < 0.001).
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