Three-dimensional culture systems for the expansion of pluripotent embryonic stem cells
Article first published online: 29 JUN 2010
Copyright © 2010 Wiley Periodicals, Inc.
Biotechnology and Bioengineering
Volume 107, Issue 4, pages 683–695, 1 November 2010
How to Cite
Storm, M. P., Orchard, C. B., Bone, H. K., Chaudhuri, J. B. and Welham, M. J. (2010), Three-dimensional culture systems for the expansion of pluripotent embryonic stem cells. Biotechnol. Bioeng., 107: 683–695. doi: 10.1002/bit.22850
- Issue published online: 13 SEP 2010
- Article first published online: 29 JUN 2010
- Manuscript Accepted: 14 JUN 2010
- Manuscript Revised: 8 JUN 2010
- Manuscript Received: 27 JAN 2010
- BBSRC Grant. Grant Number: BB/D014549/1
- embryonic stem cells;
- 3D agitated suspension culture;
Mouse embryonic stem cell (ESC) lines, and more recently human ESC lines, have become valuable tools for studying early mammalian development. Increasing interest in ESCs and their differentiated progeny in drug discovery and as potential therapeutic agents has highlighted the fact that current two-dimensional (2D) static culturing techniques are inadequate for large-scale production. The culture of mammalian cells in three-dimensional (3D) agitated systems has been shown to overcome many of the restrictions of 2D and is therefore likely to be effective for ESC proliferation. Using murine ESCs as our initial model, we investigated the effectiveness of different 3D culture environments for the expansion of pluripotent ESCs. Solohill Collagen, Solohill FACT, and Cultispher-S microcarriers were employed and used in conjunction with stirred bioreactors. Initial seeding parameters, including cell number and agitation conditions, were found to be critical in promoting attachment to microcarriers and minimizing the size of aggregates formed. While all microcarriers supported the growth of undifferentiated mESCs, Cultispher-S out-performed the Solohill microcarriers. When cultured for successive passages on Cultispher-S microcarriers, mESCs maintained their pluripotency, demonstrated by self-renewal, expression of pluripotency markers and the ability to undergo multi-lineage differentiation. When these optimized conditions were applied to unweaned human ESCs, Cultispher-S microcarriers supported the growth of hESCs that retained expression of pluripotency markers including SSEA4, Tra-1–60, NANOG, and OCT-4. Our study highlights the importance of optimization of initial seeding parameters and provides proof-of-concept data demonstrating the utility of microcarriers and bioreactors for the expansion of hESCs. Biotechnol. Bioeng. 2010;107:683–695. © 2010 Wiley Periodicals, Inc.