Cell sourcing for bone tissue engineering: Amniotic fluid stem cells have a delayed, robust differentiation compared to mesenchymal stem cells

被引:32
|
作者
Peister, Alexandra [1 ,2 ]
Woodruff, Maria A. [3 ]
Prince, Jarod J. [1 ]
Gray, Derwin P. [1 ]
Hutmacher, Dietmar W. [2 ,3 ]
Guldberg, Robert E. [2 ,4 ]
机构
[1] Morehouse Coll, Dept Biol, Atlanta, GA 30314 USA
[2] Georgia Inst Technol, Parker H Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
[3] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Kelvin Grove, Qld 4059, Australia
[4] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
关键词
OSTEOGENIC DIFFERENTIATION; IN-VITRO; STROMAL CELLS; MINERALIZATION; PROLIFERATION;
D O I
10.1016/j.scr.2011.03.001
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Cell based therapies for bone regeneration are an exciting emerging technology, but the availability of osteogenic cells is limited and an ideal cell source has not been identified. Amniotic fluid-derived stem cells (AFS) and bone-marrow derived mesenchymal stem cells (MSCs) were compared to determine their osteogenic differentiation capacity in both 2D and 3D environments. In 2D culture, the AFS cells produced more mineralized matrix but delayed peaks in osteogenic markers. Cells were also cultured on 3D scaffolds constructed of poly-c-caprolactone for 15 weeks. MSCs differentiated more quickly than AFS cells on 3D scaffolds, but mineralized matrix production slowed considerably after 5 weeks. In contrast, the rate of AFS cell mineralization continued to increase out to 15 weeks, at which time AFS constructs contained 5-fold more mineralized matrix than MSC constructs. Therefore, cell source should be taken into consideration when used for cell therapy, as the MSCs would be a good choice for immediate matrix production, but the AFS cells would continue robust mineralization for an extended period of time. This study demonstrates that stem cell source can dramatically influence the magnitude and rate of osteogenic differentiation in vitro. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:17 / 27
页数:11
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