Expansion of mouse embryonic stem cells on microcarriers

Embryonic stem (ES) cells have been shown to differentiate in vitro into a wide variety of cell types having significant potential for tissue regeneration. Therefore, the operational conditions for the ex vivo expansion and differentiation should be optimized for large‐scale cultures. The expansion of mouse ES cells has been evaluated in static culture. However, in this system, culture parameters are difficult to monitor and scaling‐up becomes time consuming. The use of stirred bioreactors facilitates the expansion of cells under controlled conditions but, for anchorage‐dependent cells, a proper support is necessary. Cytodex‐3, a microporous microcarrier made up of a dextran matrix with a collagen layer at the surface, was tested for its ability to support the expansion of the mouse S25 ES cell line in spinner flasks. The effect of inocula and microcarrier concentration on cell growth and metabolism were analyzed. Typically, after seeding, the cells exhibited a growth curve consisting of a short death or lag phase followed by an exponential phase leading to the maximum cell density of 2.5–3.9 × 106 cells/mL. Improved expansion was achieved using an inoculum of 5 × 104 cells/mL and a microcarrier concentration of 0.5 mg/mL. Medium replacement allowed the supply of the nutrients and the removal of waste products inhibiting cell growth, leading to the maintenance of the cultures in steady state for several days. These conditions favored the preservation of the S25 cells pluripotent state, as assessed by quantitative real‐time PCR and immunostaining analysis. Biotechnol. Bioeng. 2007;96:1211–1221. © 2006 Wiley Periodicals, Inc.

[1]  J. Hescheler,et al.  Tumor-induced angiogenesis studied in confrontation cultures of multicellular tumor spheroids and embryoid bodies grown from pluripotent embryonic stem cells. , 2001, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[2]  M. S. Kallos,et al.  Passaging Protocols for Mammalian Neural Stem Cells in Suspension Bioreactors , 2002, Biotechnology progress.

[3]  P. Robson,et al.  Transcriptional Regulation of Nanog by OCT4 and SOX2* , 2005, Journal of Biological Chemistry.

[4]  M. Kaufman,et al.  Establishment in culture of pluripotential cells from mouse embryos , 1981, Nature.

[5]  Peter W Zandstra,et al.  Shear‐Controlled Single‐Step Mouse Embryonic Stem Cell Expansion and Embryoid Body–Based Differentiation , 2005, Stem cells.

[6]  S Reuveny,et al.  Microcarrier culture systems. , 1990, Bioprocess technology.

[7]  S S Ozturk,et al.  Real-time monitoring and control of glucose and lactate concentrations in a mammalian cell perfusion reactor. , 1997, Biotechnology and bioengineering.

[8]  Michael S Kallos,et al.  Large‐Scale Expansion of Mammary Epithelial Stem Cell Aggregates in Suspension Bioreactors , 2008, Biotechnology progress.

[9]  D. Gottlieb,et al.  Embryonic stem cells express neuronal properties in vitro. , 1995, Developmental biology.

[10]  J. Nichols,et al.  Functional Expression Cloning of Nanog, a Pluripotency Sustaining Factor in Embryonic Stem Cells , 2003, Cell.

[11]  P. Rathjen,et al.  Directed differentiation of pluripotent cells to neural lineages: homogeneous formation and differentiation of a neurectoderm population. , 2002, Development.

[12]  M. Carpenter,et al.  38 – Characterization of Human Embryonic Stem Cells , 2004 .

[13]  P M Alves,et al.  Hydrodynamic effects on BHK cells grown as suspended natural aggregates , 1995, Biotechnology and bioengineering.

[14]  J. Miyazaki,et al.  Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells , 2000, Nature Genetics.

[15]  J. Miller,et al.  Production of human natural killer cells for adoptive immunotherapy using a computer-controlled stirred-tank bioreactor. , 1996, Journal of hematotherapy.

[16]  J. Nichols,et al.  BMP Induction of Id Proteins Suppresses Differentiation and Sustains Embryonic Stem Cell Self-Renewal in Collaboration with STAT3 , 2003, Cell.

[17]  Steve Oh,et al.  High density cultures of embryonic stem cells. , 2005, Biotechnology and bioengineering.

[18]  Russell G Foster,et al.  Experimental validation of novel and conventional approaches to quantitative real-time PCR data analysis. , 2003, Nucleic acids research.

[19]  A. Smith,et al.  Embryo-derived stem cells: of mice and men. , 2001, Annual review of cell and developmental biology.

[20]  Peter W. Zandstra,et al.  Expansion of Hematopoietic Progenitor Cell Populations in Stirred Suspension Bioreactors of Normal Human Bone Marrow Cells , 1994, Bio/Technology.

[21]  Y. Sasai,et al.  Neural conversion of ES cells by an inductive activity on human amniotic membrane matrix. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[22]  D. Lauffenburger,et al.  Supplementation-dependent differences in the rates of embryonic stem cell self-renewal, differentiation, and apoptosis. , 2003, Biotechnology and bioengineering.

[23]  W M Miller,et al.  Stirred culture of peripheral and cord blood hematopoietic cells offers advantages over traditional static systems for clinically relevant applications. , 1998, Biotechnology and bioengineering.

[24]  D. Henrique,et al.  Expansion and neural differentiation of embryonic stem cells in adherent and suspension cultures , 2003, Biotechnology Letters.

[25]  Lubiniecki Large scale mammalian cell culture technology. , 1990, Bioprocess technology.

[26]  G. Keller,et al.  In vitro differentiation of embryonic stem cells. , 1995, Current opinion in cell biology.

[27]  Michael S. Kallos,et al.  Effects of Hydrodynamics on Cultures of Mammalian Neural Stem Cell Aggregates in Suspension Bioreactors , 2001 .

[28]  M. Murakami,et al.  The Homeoprotein Nanog Is Required for Maintenance of Pluripotency in Mouse Epiblast and ES Cells , 2003, Cell.

[29]  C. Dehay,et al.  In vitro differentiation of embryonic stem cells into glial cells and functional neurons. , 1995, Journal of cell science.

[30]  A. Brivanlou,et al.  Molecular signature of human embryonic stem cells and its comparison with the mouse. , 2003, Developmental biology.

[31]  J. Itskovitz‐Eldor,et al.  Differences between human and mouse embryonic stem cells. , 2004, Developmental biology.

[32]  M. Koller,et al.  Growth factor consumption and production in perfusion cultures of human bone marrow correlate with specific cell production. , 1995, Experimental hematology.

[33]  M. Pfaffl,et al.  A new mathematical model for relative quantification in real-time RT-PCR. , 2001, Nucleic acids research.

[34]  R. Cherry,et al.  Transient shear stresses on a suspension cell in turbulence , 1990, Biotechnology and bioengineering.

[35]  R. Lovell-Badge,et al.  Generation of purified neural precursors from embryonic stem cells by lineage selection , 1998, Current Biology.

[36]  Michael S Kallos,et al.  Expansion of mammalian neural stem cells in bioreactors: effect of power input and medium viscosity. , 2002, Brain research. Developmental brain research.

[37]  W M Miller,et al.  Characterization of Hematopoietic Cell Expansion, Oxygen Uptake, and Glycolysis in a Controlled, Stirred‐Tank Bioreactor System , 1998, Biotechnology progress.

[38]  Austin G Smith,et al.  Niche-Independent Symmetrical Self-Renewal of a Mammalian Tissue Stem Cell , 2005, PLoS biology.

[39]  G. Martin,et al.  Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[40]  Smadar Cohen,et al.  Bioreactor cultivation enhances the efficiency of human embryoid body (hEB) formation and differentiation , 2004, Biotechnology and bioengineering.

[41]  Andre Choo,et al.  Perfusion cultures of human embryonic stem cells , 2005, Bioprocess and biosystems engineering.

[42]  A. V. van Wezel Growth of Cell-strains and Primary Cells on Micro-carriers in Homogeneous Culture , 1967, Nature.

[43]  Martin Raff,et al.  Normal timing of oligodendrocyte development from genetically engineered, lineage-selectable mouse ES cells , 2002, Journal of Cell Science.

[44]  M V Peshwa,et al.  Primary hepatocytes outperform Hep G2 cells as the source of biotransformation functions in a bioartificial liver. , 1994, Annals of surgery.

[45]  P. Alves,et al.  Culturing primary brain astrocytes under a fully controlled environment in a novel bioreactor , 2005, Journal of neuroscience research.