Differentiation of Human Bone Marrow Mesenchymal Stem Cells to Chondrocytes for Construction of Three-dimensional Cartilage Tissue

被引:14
作者
Chikayoshi Matsuda
Mutsumi Takagi
Takako Hattori
Shigeyuki Wakitani
Toshiomi Yoshida
机构
[1] Osaka University,International Center for Biotechnology
[2] Osaka-Minami National Hospital,Department of Orthopedic Surgery
[3] Shinshu University School of Medicine,Orthopedic Surgery
[4] Hokkaido University,Division of Biotechnology and Molecular Chemistry, Graduate School of Engineering
来源
Cytotechnology | 2005年 / 47卷
关键词
Chondrocyte; Differentiation; Mesenchymal stem cell; Three-dimension;
D O I
暂无
中图分类号
学科分类号
摘要
A differentiation method of human bone marrow mesenchymal stem cells (MSCs) to chondrocytes was developed for the construction of a three-dimensional (3D) cartilage tissue. The adhesive cells, which were isolated from a human bone marrow aspirate were embedded in type I collagen in a poly-l-lactate-glycolic acid copolymer (PLGA) mesh and cultivated for 4 week together with growth factors. The degree of cellular differentiation was estimated by quantitative RT-PCR of aggrecan and type II collagen mRNAs and by staining with Safranin O. The 3D culture showed a higher degree of differentiation even without growth factors than the conventional pellet culture with growth factors, namely, dexamethasone and transforming growth factor (TGF)-β 3. The 3D culture for 2 week with the combined addition of dexamethasone, TGF-β 3, and insulin-like growth factor (IGF)-I reached a 30% expression of aggrecan mRNA compared with that in primary human chondrocytes, while the aggrecan mRNA expression in the conventional pellet culture was less than 2%. The sequential two-step differentiation cultivation, during which the cells were cultivated in 3D for 1 week after the conventional two-dimensional (2D) culture for 1 week, could markedly accelerate the expression of aggrecan mRNA compared with the 3D cultivation for 2 week.
引用
收藏
页码:11 / 17
页数:6
相关论文
共 89 条
[1]  
Alastair M.(1998)Chondrogenic differentiation of cultured human mesenchymal stem cells from marrow Tissue Eng. 4 415-428
[2]  
Mackey Stephen C.(2000)Effect of transforming growth factor-β 1 on chondrogenic differentiation of cultured equine mesenchymal stem cells Am. J. Veterinary Res. 9 1003-1010
[3]  
Beck J.(2001)Chondrocytic differentiation of mesenchymal stem cells sequentially exposed to transforming growth factor-β 1 in monolayer and insulin-like growth factor-I in a three-dimensional matrix J. Orthop. Res. 19 738-749
[4]  
Mary M.(1999)The monoclonal antibody SH-2, raised against human mesenchymal stem cells, recognizes an epitope on endoglin (CD105) Biochem. Biophys. Res. Commun. 265 134-139
[5]  
Frank P.B.(1997)Growth kinetics, self-renewal, and the osteogenic potential of purified human mesenchymal stem cells during extensive subcultivation and following cryopreservation J. Cell. Biochem. 64 278-294
[6]  
Clinton O.C.(1998)Bone regeneration by implantation of purifiedculture-expanded human mesenchymal stem cells J. Orthop. Res. 16 155-162
[7]  
Mark F.P.(1991)Mesenchymal stem cells J. Orthop. Res. 9 641-650
[8]  
Allison A.W.(1996)Differentiation potential of conditionally immortalized mesenchymal progenitor cells from adult marrow of a H-2K J.␣Cell. Physiol. 167 523-538
[9]  
Alan J.N.(2001)-tsA58 transgenic mouse Exp. Cell Res. 268 189-200
[10]  
Brent D.B.-T.(1995)Chondrogenic differentiation of mesenchymal stem cells from bone marrow: differentiation-dependent gene expression of matrix components Bone Marrow Transpl. 16 557-564