Redifferentiation of dedifferentiated human articular chondrocytes: comparison of 2D and 3D cultures

被引:437
作者
Caron, M. M. J. [1 ]
Emans, P. J. [1 ]
Coolsen, M. M. E. [1 ]
Voss, L. [1 ]
Surtel, D. A. M. [1 ]
Cremers, A. [1 ]
van Rhijn, L. W. [1 ]
Welting, T. J. M. [1 ]
机构
[1] Maastricht Univ, Med Ctr, Dept Orthopaed Surg, CAPHRI Sch Publ Hlth & Primary Care, NL-6202 AZ Maastricht, Netherlands
关键词
Dedifferentiated human articular chondrocyte; Chondrogenic redifferentiation; Alginate culture; Pellet culture; Monolayer culture; Protein expression; MESENCHYMAL STEM-CELLS; IN-VITRO; SULFATED GLYCOSAMINOGLYCANS; ENDOCHONDRAL OSSIFICATION; PROTEOGLYCAN PHENOTYPE; CARTILAGE PHENOTYPE; MATRIX COMPONENTS; MONOLAYER-CULTURE; GENE-EXPRESSION; OXYGEN-TENSION;
D O I
10.1016/j.joca.2012.06.016
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
100224 [整形外科学];
摘要
Objective: Three-dimensional (3D) cultures are widely used to redifferentiate chondrocytes. However, the rationale behind the choice for 3D above two-dimensional (2D) cultures is poorly systematically investigated and mainly based on mRNA expression and glycosaminoglycan (GAG) content. The objective was to determine the differential redifferentiation characteristics of human articular chondrocytes (HACs) in monolayer, alginate beads and pellet culture by investigating mRNA expression, protein expression, GAG content and cell proliferation. Design: Dedifferentiated HACs from six individuals were redifferentiated in identical medium conditions for 7 days in monolayer, alginate beads or pellet culture. Read-out parameters were expression of chondrogenic and hypertrophic mRNAs and proteins, GAG content and cell proliferation. Results: 3D cultures specifically expressed chondrogenic mRNAs [collagen type II (COL2A1), SRY (sex determining region Y)-box 9 (SOX9), aggrecan (ACAN)), whereas 2D cultures did not. Hypertrophic mRNAs (collagen type X (COL10A1), runt-related transcription factor 2 (RUNX2), matrix metalloproteinase 13 (MMP13), vascular endothelial growth factor A (VEGFA), osteopontin (OPN), alkaline phosphatase (ALP)) were highly increased in 2D cultures and lower in 3D cultures. Collagen type I (COL1A1) mRNA expression was highest in 3D cultures. Protein expression supports most of the mRNA data, although an important discrepancy was found between mRNA and protein expression of COL2A1 and SOX9 in monolayer culture, stressing on the importance of protein expression analysis. GAG content was highest in 3D cultures, whereas chondrocyte proliferation was almost specific for 2D cultures. Conclusions: For redifferentiation of dedifferentiated HACs, 3D cultures exhibit the most potent chondrogenic potential, whereas a hypertrophic phenotype is best achieved in 2D cultures. This is the first human study that systematically evaluates the differences between proliferation, GAG content, protein expression and mRNA expression of commonly used 2D and 3D chondrocyte culture techniques. (C) 2012 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1170 / 1178
页数:9
相关论文
共 59 条
[1]
AULTHOUSE AL, 1989, IN VITRO CELL DEV B, V25, P659
[2]
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
[3]
INDEPENDENT REGULATION OF COLLAGEN TYPES BY CHONDROCYTES DURING THE LOSS OF DIFFERENTIATED FUNCTION IN CULTURE [J].
BENYA, PD ;
PADILLA, SR ;
NIMNI, ME .
CELL, 1978, 15 (04) :1313-1321
[4]
DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS [J].
BENYA, PD ;
SHAFFER, JD .
CELL, 1982, 30 (01) :215-224
[5]
Pellet Culture Elicits Superior Chondrogenic Redifferentiation than Alginate-Based Systems [J].
Bernstein, Peter ;
Dong, Meng ;
Corbeil, Denis ;
Gelinsky, Michael ;
Guenther, Klaus-Peter ;
Fickert, Stefan .
BIOTECHNOLOGY PROGRESS, 2009, 25 (04) :1146-1152
[6]
Expression of a stable articular cartilage phenotype without evidence of hypertrophy by adult human articular chondrocytes in vitro [J].
Binette, F ;
McQuaid, DP ;
Haudenschild, DR ;
Yaeger, PC ;
McPherson, JM ;
Tubo, R .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1998, 16 (02) :207-216
[7]
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
[8]
Buckwalter JA, 1998, AAOS INSTR COURS LEC, V47, P477
[9]
CHONDROCYTES IN AGAROSE CULTURE SYNTHESIZE A MECHANICALLY FUNCTIONAL EXTRACELLULAR-MATRIX [J].
BUSCHMANN, MD ;
GLUZBAND, YA ;
GRODZINSKY, AJ ;
KIMURA, JH ;
HUNZIKER, EB .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1992, 10 (06) :745-758
[10]
Effects of transforming growth factor-ß subtypes on in vitro cartilage production and mineralization of human bone marrow stromal-derived mesenchymal stem cells [J].
Cals, F. L. J. ;
Hellingman, C. A. ;
Koevoet, W. ;
de Jong, R. J. Baatenburg ;
van Osch, G. J. V. M. .
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2012, 6 (01) :68-76