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

Read more

Summary

Introduction

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).

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.