Donor age and cell passage affects differentiation potential of murine bone marrow-derived stem cells

被引:373
作者
Kretlow, James D. [2 ,4 ]
Jin, Yu-Qing [1 ,4 ]
Liu, Wei [1 ,4 ]
Zhang, Wen Jie [1 ,4 ]
Hong, Tan-Hui [1 ,4 ]
Zhou, Guangdong [1 ,4 ]
Baggett, L. Scott [3 ,4 ]
Mikos, Antonios G. [2 ,4 ]
Cao, Yilin [1 ,4 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Dept Plast & Reconstruct Surg, Shanghai Key Tissue Engn Lab, Shanghai 200011, Peoples R China
[2] Rice Univ, Dept Bioengn, Houston, TX 77251 USA
[3] Rice Univ, Dept Stat, Houston, TX 77251 USA
[4] Natl Tissue Engn Ctr China, Shanghai 200240, Peoples R China
基金
美国国家卫生研究院;
关键词
D O I
10.1186/1471-2121-9-60
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Bone marrow-derived mesenchymal stem cells (BMSCs) are a widely researched adult stem cell population capable of differentiation into various lineages. Because many promising applications of tissue engineering require cell expansion following harvest and involve the treatment of diseases and conditions found in an aging population, the effect of donor age and ex vivo handling must be understood in order to develop clinical techniques and therapeutics based on these cells. Furthermore, there currently exists little understanding as to how these two factors may be influenced by one another. Results: Differences in the adipogenic, chondrogenic, and osteogenic differentiation capacity of murine MSCs harvested from donor animals of different age and number of passages of these cells were observed. Cells from younger donors adhered to tissue culture polystyrene better and proliferated in greater number than those from older animals. Chondrogenic and osteogenic potential decreased with age for each group, and adipogenic differentiation decreased only in cells from the oldest donors. Significant decreases in differentiation potentials due to passage were observed as well for osteogenesis of BMSCs from the youngest donors and chondrogenesis of the cells from the oldest donors. Conclusion: Both increasing age and the number of passages have lineage dependent effects on BMSC differentiation potential. Furthermore, there is an obvious interplay between donor age and cell passage that in the future must be accounted for when developing cell-based therapies for clinical use.
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页数:13
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