A Minimal Common Osteochondrocytic Differentiation Medium for the Osteogenic and Chondrogenic Differentiation of Bone Marrow Stromal Cells in the Construction of Osteochondral Graft

被引:0
作者
Li, Jian [1 ,2 ]
Mareddy, Shobha [1 ]
Tan, Dawn Meifang [1 ]
Crawford, Ross [1 ]
Long, Xing [2 ]
Miao, Xigeng [1 ]
Xiao, Yin [1 ,2 ]
机构
[1] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld 4059, Australia
[2] Wuhan Univ, Sch Stomatol, Wuhan 430072, Peoples R China
基金
澳大利亚研究理事会;
关键词
MESENCHYMAL STEM-CELLS; IN-VITRO; BMP-7; PROLIFERATION; COCULTURE; GROWTH; OP-1;
D O I
10.1089/ten.tea.2008.0463
中图分类号
Q813 [细胞工程];
学科分类号
摘要
To regenerate the complex tissue such as bone-cartilage construct using tissue engineering approach, controllable differentiation of bone marrow stromal cells (BMSCs) into chondrogenic and osteogenic lineages is crucially important. This study proposes to test a minimum common osteochondrocytic differentiation medium (MCDM) formulated by including common soluble supplements (dexamethasone and ascorbic acid) used to induce chondrogenic and osteogenic differentiation. The MCDM coupled with supplemented growth factors was tested for its ability to differentiate BMSCs into osteogenic and chondrogenic lineages in both two-dimensional and three-dimensional culture systems. When transforming growth factor beta 3 was added to MCDM, BMSCs differentiated to chondrocyte-like cells, evidenced by the expression of glycosaminoglycans and type II collagen, whereas osteogenic differentiation was induced by supplementing osteogenic protein-1, resulting in detectable expression of osteopontin and osteocalcin. These chondrogenic and osteogenic differentiation markers were significantly enhanced in the three-dimensional cultures compared to the two-dimensional monolayer cultures. The results achieved in this study lay a foundation for future development of osteochondral graft, which could be engineered from bilayered scaffold with spatially loaded growth factors to control BMSC differentiation.
引用
收藏
页码:2481 / 2490
页数:10
相关论文
共 36 条
[1]   Effects of transforming growth factor β1 and dexamethasone on the growth and chondrogenic differentiation of adipose-derived stromal cells [J].
Awad, HA ;
Halvorsen, YDC ;
Gimble, JM ;
Guilak, F .
TISSUE ENGINEERING, 2003, 9 (06) :1301-1312
[2]   Proliferation kinetics and differentiation potential of ex vivo expanded human bone marrow stromal cells: Implications for their use in cell therapy [J].
Banfi, A ;
Muraglia, A ;
Dozin, B ;
Mastrogiacomo, M ;
Cancedda, R ;
Quarto, R .
EXPERIMENTAL HEMATOLOGY, 2000, 28 (06) :707-715
[3]   In search of common ground [J].
Blow, Nathan .
NATURE, 2008, 451 (7180) :855-860
[4]   Chondrocyte phenotypes on different extracellular matrix monolayers [J].
Brodkin, KR ;
García, AJ ;
Levenston, ME .
BIOMATERIALS, 2004, 25 (28) :5929-5938
[5]   The effect of implants loaded with autologous mesenchymal stem cells on the healing of canine segmental bone defects [J].
Bruder, SP ;
Kraus, KH ;
Goldberg, VM ;
Kadiyala, S .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1998, 80A (07) :985-996
[6]   Biomaterials approach to expand and direct differentiation of stem cells [J].
Chai, Chou ;
Leong, Kam W. .
MOLECULAR THERAPY, 2007, 15 (03) :467-480
[7]   NOVEL BIOREACTORS FOR OSTEOCHONDRAL TISSUE ENGINEERING [J].
Chang, Chih-Hung ;
Lin, Chien-Cheng ;
Chou, Cheng-Hung ;
Lin, Feng-Huei ;
Liu, Hwa-Chang .
BIOMEDICAL ENGINEERING-APPLICATIONS BASIS COMMUNICATIONS, 2005, 17 (01) :38-43
[8]   A role for chemistry in stem cell biology [J].
Ding, S ;
Schultz, PG .
NATURE BIOTECHNOLOGY, 2004, 22 (07) :833-840
[9]   Matrix elasticity directs stem cell lineage specification [J].
Engler, Adam J. ;
Sen, Shamik ;
Sweeney, H. Lee ;
Discher, Dennis E. .
CELL, 2006, 126 (04) :677-689
[10]   Chondrogenic potential of adipose tissue-derived stromal cells in vitro and in vivo [J].
Erickson, GR ;
Gimble, JM ;
Franklin, DM ;
Rice, HE ;
Awad, H ;
Guilak, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 290 (02) :763-769