Comparison of effect of BMP-2,-4, and-6 on in vitro cartilage formation of human adult stem cells from bone marrow stroma

被引:262
作者
Sekiya, I [1 ]
Larson, BL [1 ]
Vuoristo, JT [1 ]
Reger, RL [1 ]
Prockop, DJ [1 ]
机构
[1] Tulane Univ, Hlth Sci Ctr, Ctr Gene Therapy, New Orleans, LA 70112 USA
基金
美国国家卫生研究院;
关键词
marrow stromal cells; chondrogenesis; micromass culture; BMP-2; type II collagen; human;
D O I
10.1007/s00441-004-1075-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The human adult stem cells from bone marrow stroma referred to as mesenchymal stem cells or marrow stromal cells (MSCs) are of interest because they are easily isolated and expanded and are capable of multipotential differentiation. Here, we examined the ability of recombinant human bone morphogenetic protein (BMP)-2, -4, and -6 to enhance in vitro cartilage formation of MSCs. Human MSCs were isolated from bone marrow taken from normal adult donors. The cells were pelleted and cultured for 21 days in chondrogenic medium containing transforming growth factor beta 3 and dexamethasone with or without BMP-2, -4, or -6. All the BMPs tested increased chondrogenic differentiation as assayed by immunohistochemistry and by the size and weight of the cartilage synthesized. However, BMP-2 was the most effective. Microarray analyses of approximately 12,000 genes and reverse transcription-polymerase chain reaction assays established that the critical genes for cartilage synthesis were expressed in the expected time sequence in response to BMP-2. The tissue engineering of autologous cartilage derived from MSCs in vitro for transplantation will be a future alternative for patients with cartilage injuries. To obtain large amounts of cartilage rich in proteoglycans, the use of BMP-2 is recommended, instead of BMP-4 or -6.
引用
收藏
页码:269 / 276
页数:8
相关论文
共 32 条
[1]   The transcrintion factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6 [J].
Akiyama, H ;
Chaboissier, MC ;
Martin, JF ;
Schedl, A ;
de Crombrugghe, B .
GENES & DEVELOPMENT, 2002, 16 (21) :2813-2828
[2]   Cloning of the human prolyl 4-hydroxylase alpha subunit isoform alpha(II) and characterization of the type II enzyme tetramer - The alpha(I) and alpha(II) subunits do not form a mixed alpha(I)alpha(II)beta(2) tetramer [J].
Annunen, P ;
Helaakoski, T ;
Myllyharju, J ;
Veijola, J ;
Pihlajaniemi, T ;
Kivirikko, KI .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (28) :17342-17348
[3]   TREATMENT OF DEEP CARTILAGE DEFECTS IN THE KNEE WITH AUTOLOGOUS CHONDROCYTE TRANSPLANTATION [J].
BRITTBERG, M ;
LINDAHL, A ;
NILSSON, A ;
OHLSSON, C ;
ISAKSSON, O ;
PETERSON, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (14) :889-895
[4]   Regulatory mechanisms in the pathways of cartilage and bone formation [J].
de Crombrugghe, B ;
Lefebvre, W .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (06) :721-727
[5]  
DELEBVRE V, 2001, OSTEOARTHR CARTILAGE, V9, pS69
[6]   S100-ALPHA, CAPL, AND CACY - MOLECULAR-CLONING AND EXPRESSION ANALYSIS OF 3 CALCIUM-BINDING PROTEINS FROM HUMAN HEART [J].
ENGELKAMP, D ;
SCHAFER, BW ;
ERNE, P ;
HEIZMANN, CW .
BIOCHEMISTRY, 1992, 31 (42) :10258-10264
[7]   TYROSINE-RICH ACIDIC MATRIX PROTEIN (TRAMP) IS A TYROSINE-SULFATED AND WIDELY DISTRIBUTED PROTEIN OF THE EXTRACELLULAR-MATRIX [J].
FORBES, EG ;
CRONSHAW, AD ;
MACBEATH, JRE ;
HULMES, DJS .
FEBS LETTERS, 1994, 351 (03) :433-436
[8]  
HANGODY L, 2001, CLIN ORTHOP S, V391, P328
[9]   FIBROMODULIN DISTRIBUTION AND ASSOCIATION WITH COLLAGEN [J].
HEDLUND, H ;
MENGARELLIWIDHOLM, S ;
HEINEGARD, D ;
REINHOLT, FP ;
SVENSSON, O .
MATRIX BIOLOGY, 1994, 14 (03) :227-232
[10]   Differentiation plasticity of chondrocytes derived from mouse embryonic stem cells [J].
Hegert, C ;
Kramer, J ;
Hargus, G ;
Müller, J ;
Guan, K ;
Wobus, AM ;
Müller, PK ;
Rohwedel, J .
JOURNAL OF CELL SCIENCE, 2002, 115 (23) :4617-4628