The use of mesenchymal stem cells for chondrogenesis

被引:221
作者
Pelttari, Karoliina [1 ]
Steck, Eric [1 ]
Richter, Wiltrud [1 ]
机构
[1] Orthopaed Univ Hosp Heidelberg, Div Expt Orthopaed, Heidelberg, Germany
来源
INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED | 2008年 / 39卷
关键词
mesenchymal stem cells; chondrogenesis; hyaline cartilage; repair; endochondral bone formation; autologous chondrocytes transplantation; hypertrophy; osteochondral defects; bone marrow; adipose tissue;
D O I
10.1016/j.injury.2008.01.038
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
The application of autologous chondrocytes in cartilage repair procedures is associated with several disadvantages, including injury of healthy cartilage in a preceding surgery frequently resulting in formation of inferior fibrocartilage at defect sites. In order to improve the quality of regeneration, adult mesenchymal stem cells (MSC) are regarded as a promising alternative. The great challenge, when considering MSC for articular cartilage repair, is to generate cells with features of stable chondrocytes which are resistant to hypertrophy and terminal differentiation, as found in hyaline articular cartilage. Common in vitro protocols for chondrogenic differentiation of MSC successfully induce expression of multiple cartilage-specific molecules, including collagen type 11 and aggrecan, and result in a chondrocyte-like phenotype. However, in vitro chondrogenesis of MSC additionally promotes induction of fibrocartilage- like features such as expression of collagen type 1, and hypertrophy, as demonstrated by up-regulation of collagen type X, MMP13 and ALP-activity. As a consequence, differentiated MSC pellets undergo mineralisation and vascularisation after ectopic transplantation in a process similar to endochondral ossification. This review discusses the complexity and entailed challenges when considering MSC from various sources for clinical application and the necessity to optimise chondrogenesis by repressing hypertrophy to obtain functional and suitable cells for cartilage repair.
引用
收藏
页码:S58 / S65
页数:8
相关论文
共 65 条
[1]   The fate of the terminally differentiated chondrocyte: Evidence for microenvironmental regulation of chondrocyte apoptosis [J].
Adams, CS ;
Shapiro, IM .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 2002, 13 (06) :465-473
[2]  
Angele P, 2004, BIORHEOLOGY, V41, P335
[3]   Adult mesenchymal stem cells: characterization, differentiation, and application in cell and gene therapy [J].
Baksh, D ;
Song, L ;
Tuan, RS .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (03) :301-316
[4]   Chondrogenic differentiation of mesenchymal stem cells from bone marrow: Differentiation-dependent gene expression of matrix components [J].
Barry, F ;
Boynton, RE ;
Liu, BS ;
Murphy, JM .
EXPERIMENTAL CELL RESEARCH, 2001, 268 (02) :189-200
[5]   A prospective, randomised comparison of autologous chondrocyte implantation versus mosaicplasty for osteochondral defects in the knee [J].
Bentley, G ;
Biant, LC ;
Carrington, RWJ ;
Akmal, M ;
Goldberg, A ;
Williams, AM ;
Skinner, JA ;
Pringle, J .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2003, 85B (02) :223-230
[6]   DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS [J].
BENYA, PD ;
SHAFFER, JD .
CELL, 1982, 30 (01) :215-224
[7]   Molecular analysis of expansion, differentiation, and growth factor treatment of human chondrocytes identifies differentiation markers and growth-related genes [J].
Benz, K ;
Breit, S ;
Lukoschek, M ;
Mau, H ;
Richter, W .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 293 (01) :284-292
[8]   Osteoprogenitor cells within skeletal muscle [J].
Bosch, P ;
Musgrave, DS ;
Lee, JY ;
Cummins, J ;
Shuler, F ;
Ghivizzani, SC ;
Evans, C ;
Robbins, PD ;
Huard, J .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2000, 18 (06) :933-944
[9]   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
[10]  
Brittberg M, 1999, CLIN ORTHOP RELAT R, pS147