Simultaneous expansion and harvest of hematopoietic stem cells and mesenchymal stem cells derived from umbilical cord blood

被引:0
作者
Song Kedong
Fan Xiubo
Liu Tianqing
Hugo M. Macedo
Jiang LiLi
Fang Meiyun
Shi Fangxin
Ma Xuehu
Cui Zhanfeng
机构
[1] Dalian University of Technology,Dalian R&D Center for Stem Cell and Tissue Engineering
[2] Imperial College London,Biological Systems Engineering Laboratory, Department of Chemical Engineering
[3] First Affiliated Hospital,Department of Hematology
[4] Dalian Medical University,Department of Obstetrics and Gynecology
[5] First Affiliated Hospital,Oxford Centre for Tissue Engineering and Bioprocessing
[6] Dalian Medical University,undefined
[7] University of Oxford,undefined
来源
Journal of Materials Science: Materials in Medicine | 2010年 / 21卷
关键词
Hematopoietic Stem Cell Transplantation; CD105; Umbilical Cord Blood; Stem Cell Factor; Spinner Flask;
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学科分类号
摘要
The simultaneous expansion and harvest of hematopoietic stem cells and mesenchymal stem cells derived from umbilical cord blood were carried out using bioreactors. The co-culture of umbilical cord blood (UCB)-derived hematopoietic stem cells (HSCs) and mesenchymal stem cells (MSCs) was performed within spinner flasks and a rotating wall vessel (RWV) bioreactor using glass-coated styrene copolymer (GCSC) microcarriers. The medium used was composed of serum-free IMDM containing a cocktail of SCF 15 ng·mL−1, FL 5 ng·mL−1, TPO 6 ng·mL−1, IL-3 15 ng·mL−1, G-CSF 1 ng·mL−1 and GM-CSF 5 ng·mL−1. Accessory stromal cells derived from normal allogeneic adipose tissue were encapsulated in alginate-chitosan (AC) beads and used as feeding cells. The quality of the harvested UCB-HSCs and MSCs was assessed by immunophenotype analysis, methylcellulose colony and multi-lineage differentiation assays. After 12 days of culture, the fold-expansion of total cell numbers, colony-forming units (CFU-C), CD34+/CD45+/CD105− (HSCs) cells and CD34−/CD45−/CD105+ (MSCs) cells using the RWV bioreactor were (3.7 ± 0.3)- , (5.1 ± 1.2)- , (5.2 ± 0.4)- , and (13.9 ± 1.2)-fold respectively, significantly better than those obtained using spinner flasks. Moreover, UCB-HSCs and UCB-MSCs could be easily separated by gravity sedimentation after the co-culture period as only UCB-MSCs adhered on to the microcarriers. Simultaneously, we found that the fibroblast-like cells growing on the surface of the GCSC microcarriers could be induced and differentiated towards the osteoblastic, chondrocytic and adipocytic lineages. Phenotypically, these cells were very similarly to the MSCs derived from bone marrow positively expressing the MSCs-related markers CD13, CD44, CD73 and CD105, while negatively expressing the HSCs-related markers CD34, CD45 and HLA-DR. It was thus demonstrated that the simultaneous expansion and harvest of UCB-HSCs and UCB-MSCs is possible to be accomplished using a feasible bioreactor culture system such as the RWV bioreactor with the support of GCSC microcarriers.
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页码:3183 / 3193
页数:10
相关论文
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