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Tissue Engineering
The Chondrocyte: Biology and Clinical Application
To cite this article:
Zhen Lin, Craig Willers, Jiake Xu, Ming-Hao Zheng.
Tissue Engineering.
July 2006,
12(7): 1971-1984.
doi:10.1089/ten.2006.12.1971.
Published in Volume: 12 Issue 7: August 4, 2006
Zhen Lin Department of Orthopaedic Surgery, Faculty of Medicine and Dentistry, University of Western Australia, Western Australia 6009, Australia. Craig Willers Department of Orthopaedic Surgery, Faculty of Medicine and Dentistry, University of Western Australia, Western Australia 6009, Australia. Jiake Xu Department of Orthopaedic Surgery, Faculty of Medicine and Dentistry, University of Western Australia, Western Australia 6009, Australia. Prof. Ming-Hao Zheng, PhD, DM, FRCPathDepartment of Orthopaedic Surgery, Faculty of Medicine and Dentistry, University of Western Australia, Western Australia 6009, Australia. Chondrocyte is a unique cell type in articular cartilage tissue and is essential for cartilage formation and functionality. It arises from mesenchymal stem cells (MSCs) and is regulated by a series of cytokine and transcription factor interactions, including the transforming growth factor-β super family, fibroblast growth factors, and insulin-like growth factor-1. To understand the biomechanisms of the chondrocyte differentiation process, various cellular model systems have been employed, such as primary chondrocyte culture, clonal normal cell lines (HCS-2/8, Ch-1, ATDC5, CFK-2, and RCJ3.1C5.18), and transformed clonal cell lines (T/C-28a2, T/C-28a4, C-28/I2, tsT/AC62, and HPV-16 E6/E7). Additionally, cell culture methods, including conventional monolayer culture, three-dimensional scaffold culture, bioreactor culture, pellet culture, and organ culture, have been established to create stable environments for the expansion, phenotypic maintenance, and subsequent biological study of chondrocytes for clinical application. Knowledge gained through these study systems has allowed for the use of chondrocytes in orthopedics for the treatment of cartilage injury and epiphyseal growth plate defects using tissueengineering approaches. Furthermore, the potential of chondrocyte implantation for facial reconstruction, the treatment of long segmental tracheal defects, and urinary incontinence and vesicoureteral reflux are being investigated. This review summarizes the present study of chondrocyte biology and the potential uses of this cell in orthopedics and other disciplines.  This paper was cited by:Cartilage replacement by use of hybrid systems of autologous cells and polyethylene: an experimental study Ilona Schoen, Torsten Rahne, Annekatrin Markwart, Kerstin Neumann, Alexander Berghaus, Ernst Roepke Journal of Materials Science: Materials in Medicine. Jun 2009 CrossRef Cartilage Tissue Formation Using Redifferentiated Passaged Chondrocytes In Vitro Nazish Ahmed, Lu Gan, Andras Nagy, Jianing Zheng, Chen Wang, Rita A. Kandel Tissue Engineering Part A. Mar 2009, Vol. 15, No. 3: 665-673 Abstract | Full Text PDF or HTML | Reprints & PermissionsThe Role of the Biochemical and Biophysical Environment in Chondrogenic Stem Cell Differentiation Assays and Cartilage Tissue Engineering Kristin E. Wescoe, Rebecca C. Schugar, Constance R. Chu, Bridget M. Deasy Cell Biochemistry and Biophysics. Nov 2008, Vol. 52, No. 2: 85-102 CrossRef Gene expression profiles of human chondrocytes during passaged monolayer cultivation Zhen Lin, Jonathan B. Fitzgerald, Jiake Xu, Craig Willers, David Wood, Alan J. Grodzinsky, Ming H. Zheng Journal of Orthopaedic Research. Oct 2008, Vol. 26, No. 9: 1230-1237 CrossRef Biological Treatment for Degenerative Disc Disease Yejia Zhang, Howard S. An, Chadi Tannoury, Eugene J.-M.A. Thonar, Mitchell K. Freedman, D Greg Anderson American Journal of Physical Medicine & Rehabilitation. Oct 2008, Vol. 87, No. 9: 694-702 CrossRef Roles of Wnt signalling in bone growth, remodelling, skeletal disorders and fracture repair Carmen E. Macsai, Bruce K. Foster, Cory J. Xian Journal of Cellular Physiology. Jul 2008, Vol. 215, No. 3: 578-587 CrossRef Characterization of spatial growth and distribution of chondrocyte cells embedded in collagen gels through a stereoscopic cell imaging system Masahiro Kino-oka, Yoshikatsu Maeda, Yasuaki Sato, Ali Baradar Khoshfetrat, Takeyuki Yamamoto, Katsura Sugawara, Masahito Taya Biotechnology and Bioengineering. May 2008, Vol. 99, No. 5: 1230-1240 CrossRef FBS suppresses TGF-β1-induced chondrogenesis in synoviocyte pellet cultures while dexamethasone and dynamic stimuli are beneficial Bahar Bilgen, Ester Orsini, Roy K. Aaron, Deborah McK. Ciombor Journal of Tissue Engineering and Regenerative Medicine. Dec 2007, Vol. 1, No. 6: 436-442 CrossRef Chondrocyte hypertrophy and apoptosis induced by GROα require three-dimensional interaction with the extracellular matrix and a co-receptor role of chondroitin sulfate and are associated with the mitochondrial splicing variant of cathepsin B Eleonora Olivotto, Roberta Vitellozzi, Patricia Fernandez, Elisabetta Falcieri, Michela Battistelli, Sabrina Burattini, Annalisa Facchini, Flavio Flamigni, Spartaco Santi, Andrea Facchini, Rosa Maria Borzi' Journal of Cellular Physiology. Mar 2007, Vol. 210, No. 2: 417-427 CrossRef
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