Characterization of Hematopoietic Cell Expansion, Oxygen Uptake, and Glycolysis in a Controlled, Stirred-Tank Bioreactor System

• Published in: Biotechnology progress Vol. 14; no. 3; pp. 466 - 472
• Main Authors: Collins, Paul C., Nielsen, Lars K., Patel, Sanjay D., Papoutsakis, E. Terry, Miller, William M.
• Format: Journal Article
• Language: English
• Published: USA American Chemical Society 01.05.1998; American Institute of Chemical Engineers
• Subjects: Animal cells; Biological and medical sciences; Bioreactors; Biotechnology; Eukaryotic cell cultures; Fundamental and applied biological sciences. Psychology; Glycolysis; Hematopoietic Stem Cells - physiology; Humans; Methods. Procedures. Technologies; Miscellaneous; Oxygen Consumption; Human; Cell culture; Bioreactor; Animal; Hematopoietic cell; Glycolysis; CFU-GM-Cell; Oxygen consumption; Umbilical cord; Metabolism; Stirred tank reactor; Blood
• ISSN: 8756-7938; 1520-6033
• DOI: 10.1021/bp980032e

Cultures of umbilical cord blood and mobilized peripheral blood mononuclear cells were carried out in a stirred bioreactor with pH and dissolved oxygen control. Expansion of total cells and colony‐forming units granulocyte‐macrophage was greatly enhanced by the use of a cell‐dilution feeding protocol (as compared to a cell‐retention feeding protocol). The specific oxygen consumption rate (qO2) for these cultures ranged from 1.7 × 10‐8 to 1.2 × 10‐7 μmol/(cell·h). The maximum in qO2 for each culture closely corresponded with the maximum percentage of progenitor or colony‐forming cells (CFCs) present in the culture. The maximum qO2 values are slightly less than those reported for hybridomas, while the lowest qO2 values are somewhat greater than those reported for mature granulocytes. Examination of the ratio of lactate production to oxygen consumption in these cultures suggests that post‐progenitor cells of the granulomonocytic lineage obtain a greater portion of their energy from glycolysis than do CFCs. The different metabolic profiles of CFCs and more mature cells suggest that monitoring the uptake or production of oxygen, lactate, and other metabolites will allow estimation of the content of several cell types in culture.