Defective flow space limits the scaling up of turbulence bioreactors for platelet generation

• Published in: Communications engineering Vol. 3; no. 1; pp. 77 - 12
• Main Authors: Okamoto, Haruki, Fujio, Kosuke, Nakamura, Sou, Harada, Yasuo, Hayashi, Hideki, Higashi, Natsumi, Ninomiya, Atsushi, Tanaka, Ryota, Sugimoto, Naoshi, Takayama, Naoya, Kaneda, Atsushi, Sawaguchi, Akira, Kato, Yoshikazu, Eto, Koji
• Format: Journal Article
• Language: English
• Published: London Springer Nature B.V 01.12.2024; Nature Publishing Group UK; Nature Portfolio
• Subjects: Antigens; Bioreactors; Clinical trials; Efficiency; Energy; Flow cytometry; Fluid dynamics; Impellers; Manufacturing; Scaling up; Shear stress; Simulation; Stem cells; Thrombocytopenia; Turbulence; Turbulent flow
• ISSN: 2731-3395
• DOI: 10.1038/s44172-024-00219-y

To complement donor-dependent platelets supplies, we previously developed an ex vivo manufacturing system using induced pluripotent stem cell (iPSC)-derived expandable immortalized megakaryocyte progenitor cell lines (imMKCLs), and a turbulent flow bioreactor to generate iPSC-derived platelets products (iPSC-PLTs). However, the tank size of the bioreactor was limited to 10 L. Here we examined the feasibility of scaling up to 50 L with reciprocal motion by two impellers. Under optimized turbulence parameters corresponding to 10 L bioreactor, 50 L bioreactor elicited iPSC-PLTs with intact in vivo hemostatic function but with less production efficiency. This insufficiency was caused by increased defective turbulent flow space. A computer simulation proposed that designing 50 L turbulent flow bioreactor with three impellers or a new bioreactor with a modified rotating impeller and unique structure reduces this space. These findings indicate that large-scale iPSC-PLTs manufacturing from cultured imMKCLs requires optimization of the tank structure in addition to optimal turbulent energy and shear stress.Haruki Okamoto and colleagues demonstrate that tank structure is crucial for large-scale platelet production from cultured immortalized megakaryocyte progenitor cell lines, due to the increase in defective turbulent flow space. These insights could guide the development of new bioreactors with improved production efficiency.