These authors contributed equally to this work.
Special theme research article
Co-culture of hematopoietic stem cells and mesenchymal stem cells derived from umbilical cord blood using human autoserum
Article first published online: 20 SEP 2010
© 2010 Curtin University of Technology and John Wiley & Sons, Ltd.
Asia-Pacific Journal of Chemical Engineering
Volume 6, Issue 6, pages 840–849, November/December 2011
How to Cite
Song, K., Yin, Y., Lv, C., Liu, T., Macedo, H. M., Fang, M., Shi, F., Ma, X. and Cui, Z. (2011), Co-culture of hematopoietic stem cells and mesenchymal stem cells derived from umbilical cord blood using human autoserum. Asia-Pacific Jrnl of Chem. Eng, 6: 840–849. doi: 10.1002/apj.507
- Issue published online: 14 DEC 2011
- Article first published online: 20 SEP 2010
- Manuscript Accepted: 19 JUL 2010
- Manuscript Revised: 12 JUL 2010
- Manuscript Received: 31 OCT 2009
- National Science Foundation of China. Grant Numbers: 30670525, 30700181
- new teacher foundation of Ministry of Education. Grant Number: 20070141055
The feasibility of co-culturing hematopoietic stem/progenitor cells (HSPCs) and mesenchymal stem cells (MSCs) derived from human umbilical cord blood (UCB) using cytodex-3 microcarriers was investigated in this paper in order to assess this as a possibility for future clinical therapies. Considering the safety requirements of clinical applications, we have tried to use human autologous serum (HAS), collected from UCB, to replace the widely used fetal bovine serum (FBS). Moreover, both UCB-hematopoietic stem cells (HSCs) and UCB-MSCs could be harvested simultaneously after their ex vivo culture. In addition, the two different types of stem cells could be easily separated by sedimentation after the co-culture due to the distinct weight differences between cytodex-3 microcarriers (containing adherent MSCs) and the suspended HSCs. To optimize the culture conditions, we have assessed the effect of the concentration of HAS (2.8, 5.6, 8.3 and 11.1%) on the expansion of UCB-MSCs and UCB-HSCs. The results have indicated that the expansion of UCB-HSCs supplied with 5.6% autoserum was at least (1.88 ± 0.33)-fold, better than in the other groups, while it had no to little effect on the expansion of UCB-MSCs. We hence conclude that the optimal concentration of HAS for the co-culture conditions herein reported is 5.6%. Finally, the co-culture system we have developed and herein report is feasible to provide expanded UCB-HSPCs and UCB-MSCs for clinical applications, especially the former. © 2010 Curtin University of Technology and John Wiley & Sons, Ltd.