Rapid phenotypic changes in passaged articular chondrocyte subpopulations

被引:498
作者
Darling, EM [1 ]
Athanasiou, KA [1 ]
机构
[1] Rice Univ, Dept Bioengn, Houston, TX 77251 USA
关键词
articular cartilage; monolayer expansion; choudrocyte; zones; gene expression; differentiation;
D O I
10.1016/j.orthres.2004.08.008
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Articular chondrocytes are often expanded in vitro and then used to assist in healing articular cartilage defects. We investigated the extent of dedifferentiation in monolayer-passaged, zonal articular chondrocytes by using quantitative, real-time PCR. The relative gene expressions for collagen type I and II, aggrecan, and Superficial zone protein were analyzed for relevant passage numbers (P0-P4) to determine how the expansion of chondrocytes affects the expression of cartilage extracellular matrix proteins. Results reveal that dramatic changes occur as early as first passage. Furthermore, these changes are shown to persist even when the expanded cells are encapsulated in 3D, alginate beads. Successful tissue engineering and autologous cell transplantation procedures rely heavily on having a cell Source that expresses the chondrocytic phenotype. The results of this study suggest that major problems exist at the front-end of cartilage regeneration efforts. (c) 2004 Orthopaedic Research Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:425 / 432
页数:8
相关论文
共 32 条
[1]
Biodegradable implants for the treatment of osteochondral defects in a goat model [J].
Athanasiou, K ;
Korvick, D ;
Schenck, R .
TISSUE ENGINEERING, 1997, 3 (04) :363-373
[2]
Benninghoff A., 1925, Z ANAT ENTWICKLUNGS, V76, P43, DOI [DOI 10.1007/BF02134417, 10.1007/BF02134417]
[3]
DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS [J].
BENYA, PD ;
SHAFFER, JD .
CELL, 1982, 30 (01) :215-224
[4]
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
[5]
Buckwalter JA, 1998, AAOS INSTR COURS LEC, V47, P477
[6]
Biomechanical strategies for articular cartilage regeneration [J].
Darling, EM ;
Athanasiou, KA .
ANNALS OF BIOMEDICAL ENGINEERING, 2003, 31 (09) :1114-1124
[7]
Articular cartilage Bioreactors and bioprocesses [J].
Darling, EM ;
Athanasiou, KA .
TISSUE ENGINEERING, 2003, 9 (01) :9-26
[8]
Zonal and topographical differences in articular cartilage gene expression [J].
Darling, EM ;
Hu, JCY ;
Athanasiou, KA .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2004, 22 (06) :1182-1187
[9]
Optimization of chondrocyte expansion in culture -: Effect of TGFβ-2, bFGF and L-ascorbic acid on bovine articular chondrocytes [J].
de Haart, M ;
Marijnissen, WJCM ;
van Osch, GJVM ;
Verhaar, JAN .
ACTA ORTHOPAEDICA SCANDINAVICA, 1999, 70 (01) :55-61
[10]
EROSCHENKO V, 1996, ATLAS HISTOLOGY FUNC, P40