Extracellular matrix production in vitro in cartilage tissue engineering

被引:53
作者
Chen, Jie-Lin [1 ,2 ,3 ]
Duan, Li [1 ,2 ,3 ]
Zhu, Weimin [1 ,3 ]
Xiong, Jianyi [1 ,3 ]
Wang, Daping [1 ,3 ]
机构
[1] Shenzhen Univ, Affiliated Hosp 1, Shenzhen Peoples Hosp 2, Shenzhen Key Lab Tissue Engn, Shenzhen 518035, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Sch Med, Guangzhou 510182, Guangdong, Peoples R China
[3] Shenzhen Second Peoples Hosp, Dept Orthoped, Shenzhen 518035, Guangdong, Peoples R China
关键词
Cartilage; Tissue engineering; Extracellular matrix; Collagen type II; MESENCHYMAL STEM-CELLS; TRANSFORMING GROWTH-FACTOR-BETA-1 TGF-BETA-1; AUTOLOGOUS CHONDROCYTE IMPLANTATION; RABBIT ARTICULAR CHONDROCYTES; INTERMITTENT HYDROSTATIC-PRESSURE; BONE MORPHOGENETIC PROTEIN-2; II COLLAGEN-SYNTHESIS; CHONDROGENIC DIFFERENTIATION; GENE-EXPRESSION; GROWTH-FACTOR;
D O I
10.1186/1479-5876-12-88
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cartilage tissue engineering is arising as a technique for the repair of cartilage lesions in clinical applications. However, fibrocartilage formation weakened the mechanical functions of the articular, which compromises the clinical outcomes. Due to the low proliferation ability, dedifferentiation property and low production of cartilage-specific extracellular matrix (ECM) of the chondrocytes, the cartilage synthesis in vitro has been one of the major limitations for obtaining high-quality engineered cartilage constructs. This review discusses cells, biomaterial scaffolds and stimulating factors that can facilitate the cartilage-specific ECM production and accumulation in the in vitro culture system. Special emphasis has been put on the factors that affect the production of ECM macromolecules such as collagen type II and proteoglycans in the review, aiming at providing new strategies to improve the quality of tissue-engineered cartilage.
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页数:9
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共 91 条
[1]   Cryopreservation of articular cartilage [J].
Abazari, Alireza ;
Jomha, Nadr M. ;
Elliott, Janet A. W. ;
McGann, Locksley E. .
CRYOBIOLOGY, 2013, 66 (03) :201-209
[2]   Growth Factor Directed Chondrogenic Differentiation of Porcine Bone Marrow-Derived Progenitor Cells [J].
Abukawa, Harutsugi ;
Oriel, Brad S. ;
Leaf, Jeremy ;
Vacanti, Joseph P. ;
Kaban, Leonard B. ;
Troulis, Maria J. ;
Hartnick, Christopher J. .
JOURNAL OF CRANIOFACIAL SURGERY, 2013, 24 (03) :1026-1030
[3]   Influence of cryopreservation, cultivation time and patient's age on gene expression in Hyalograft® C cartilage transplants [J].
Albrecht, Christian ;
Tichy, Brigitte ;
Nuernberger, Sylvia ;
Zak, Lukas ;
Handl, Markus Johannes ;
Marlovits, Stefan ;
Aldrian, Silke .
INTERNATIONAL ORTHOPAEDICS, 2013, 37 (11) :2297-2303
[4]   DETECTION OF ABNORMALITIES IN THE SUPERFICIAL ZONE OF CARTILAGE REPAIRED USING A TISSUE ENGINEERED CONSTRUCT DERIVED FROM SYNOVIAL STEM CELLS [J].
Ando, Wataru ;
Fujie, Hiromichi ;
Moriguchi, Yu ;
Nansai, Ryosuke ;
Shimomura, Kazunori ;
Hart, David A. ;
Yoshikawa, Hideki ;
Nakamura, Norimasa .
EUROPEAN CELLS & MATERIALS, 2012, 24 :292-307
[5]   Expansion on specific substrates regulates the phenotype and differentiation capacity of human articular chondrocytes [J].
Barbero, Andrea ;
Grogan, Shawn Patrick ;
Mainil-Varlet, Pierre ;
Martin, Ivan .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2006, 98 (05) :1140-1149
[6]   Extracellular matrix scaffolds for cartilage and bone regeneration [J].
Benders, Kim E. M. ;
van Weeren, P. Rene ;
Badylak, Stephen F. ;
Saris, Daniel B. F. ;
Dhert, Wouter J. A. ;
Malda, Jos .
TRENDS IN BIOTECHNOLOGY, 2013, 31 (03) :169-176
[7]   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
[8]   Wavy-walled bioreactor supports increased cell proliferation and matrix deposition in engineered cartilage constructs [J].
Bueno, EM ;
Bilgen, B ;
Barabino, GA .
TISSUE ENGINEERING, 2005, 11 (11-12) :1699-1709
[9]   Down-regulation of human type II collagen gene expression by transforming growth factor-β1 (TGF-β1) in articular chondrocytes involves SP3/SP1 ratio [J].
Chadjichristos, C ;
Ghayor, C ;
Herrouin, JF ;
Ala-Kokko, L ;
Suske, G ;
Pujol, JP ;
Galéra, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (46) :43903-43917
[10]   Evaluating osteochondral defect repair potential of autologous rabbit bone marrow cells on type II collagen scaffold [J].
Chen, Wei-Chuan ;
Yao, Chao-Ling ;
Wei, Yu-Hong ;
Chu, I-Ming .
CYTOTECHNOLOGY, 2011, 63 (01) :13-23