Osteogenic Differentiation of Bone Marrow Stromal Cells Induced by Coculture with Chondrocytes Encapsulated in Three-Dimensional Matrices

被引:25
|
作者
Thompson, Andrew D. [2 ]
Betz, Martha W. [1 ]
Yoon, Diana M. [3 ]
Fisher, John P. [1 ]
机构
[1] Univ Maryland, Fischell Dept Bioengn, College Pk, MD 20742 USA
[2] Univ Maryland, Dept Cell Biol & Genet, College Pk, MD 20742 USA
[3] Univ Maryland, Dept Chem & Biomol Engn, College Pk, MD 20742 USA
基金
美国国家科学基金会;
关键词
MESENCHYMAL STEM-CELLS; IN-VITRO; NITRIC-OXIDE; EXPRESSION; COLLAGEN; MINERALIZATION; OSTEOBLASTS; CULTURES; PHENOTYPE; PROTEINS;
D O I
10.1089/ten.tea.2007.0275
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Endochondral ossification implicates chondrocyte signaling as an important factor in directing the osteogenic differentiation of mesenchymal stem cells in vivo. In this study, the osteoinductive capabilities of articular chondrocytes suspended in alginate hydrogels were analyzed via coculture with bone marrow stromal cells (BMSCs). In particular, the effect of chondrocyte coculture time on the mechanism underlying this osteogenic induction was examined. Chondrocytes were suspended in alginate beads and cultured above BMSCs in monolayer. Beads containing chondrocytes were removed after 1, 10, or 21 days of coculture. Quantitative reverse transcriptase polymerase chain reaction was used to assess the expression of alkaline phosphatase, bone morphogenetic protein-2, and osteocalcin by BMSCs after days 1, 8, 14, and 21. Calcium deposition was also assayed to characterize the extent of mineralization within cultures. Results indicate that osteogenic differentiation of BMSCs is initiated upon brief exposure to chondrocyte signaling, but requires continued exposure in order to progress fully and maintain an osteoblastic phenotype.
引用
收藏
页码:1181 / 1190
页数:10
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